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  "name": "Sterile custom surgical procedure packs:    (1) 89-10507.02, TOTAL KNEE PACK, Stonewall Jackson Hospital;  (2) 89-10508.02, LOCAL PACK, Stonewall Jackson Hospital;  (3) 89-10509.02, LAPAROTOMY PACK, Stonewall Jackson Hospital;  (4) 89-10517.04, CNRV BASIC SETUP PACK, New River Valley Medical Center;  (5) 89-10526.04, CNRV LAPAROSCOPY PACK, New River Valley Medical Center;  (6) 89-10530.04, CNRV PERIPHERAL VAS PACK, New River Valley Medical Center;  (7) 89-10532.04, CNRV SPINE PACK, New River Valley Medical Center;  (8) 89-10534.02, CMC ANTERIOR SPINE PACK, Carilion Roanoke Memorial Hosp;  (9) 89-10544.03, CORONARY BYPASS PACK PGYBK, Carilion Roanoke Memorial Hosp;  (10) 89-10545.02, CMC CRANIOTOMY PACK, Carilion Roanoke Memorial Hospital;  (11) 89-10552.02, CMC EXTREMITY PACK, Carilion Roanoke Memorial Hospital;  (12) 89-10553.02, CMC GYN LAPAROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (13) 89-10554.02, CMC GYN MAJOR PACK, Carilion Roanoke Memorial  Hospital;  (14) 89-10555.02, ORTHO MAJOR PACK, Carilion Roanoke Memorial Hospital;  (15) 89-10556.02, CMC HYSTEROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (16) 89-10558.04, CCASC LAPAROTOMY PACK, Carilion Roanoke Memorial Hospital;  (17) 89-10560.03, CMC LAPAROTOMY PACK, Carilion Roanoke Memorial Hospital;  (18) 89-10561.02, CMC LAPAROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (19) 89-10562.02, CMC MINOR ENT/PLASTIC PACK, Carilion Roanoke Memorial Hospital;  (20) 89-10564.02, CMC MAJOR PLASTIC PACK, Carilion Roanoke Memorial Hospital;  (21) 89-10569.02, CMC PEDIATRIC PACK, Carilion Roanoke Memorial Hospital;  (22) 89-10570.02, CMC POSTERIOR SPINE PACK, Carilion Roanoke Memorial Hospital;  (23) 89-10574.02, CMC SHOULDER ARTHROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (24) 89-10575.02, OWEN HIP PACK, Carilion Roanoke Memorial Hosp;  (25) 89-10576.03, THORACOSCOPY / THORACOTOMY, Carilion Roanoke Memorial Hosp;  (26) 89-10580.03, VALVE REPLACEMENT PACK PGYBK, Carilion Roanoke Memorial Hosp.",
  "description": "FDA recall Z-1691-2023 — DeRoyal Industries Inc is recalling Sterile custom surgical procedure packs:    (1) 89-10507.02, TOTAL KNEE PACK, Stonewall Jackson Hospital;  (2) 89-10508.02, LOCAL PACK, Stonewall Jackson Hospital;  (3) 89-10509.02, LAPAROTOMY PACK, Stonewall Jackson Hospital;  (4) 89-10517.04, CNRV BASIC SETUP PACK, New River Valley Medical Center;  (5) 89-10526.04, CNRV LAPAROSCOPY PACK, New River Valley Medical Center;  (6) 89-10530.04, CNRV PERIPHERAL VAS PACK, New River Valley Medical Center;  (7) 89-10532.04, CNRV SPINE PACK, New River Valley Medical Center;  (8) 89-10534.02, CMC ANTERIOR SPINE PACK, Carilion Roanoke Memorial Hosp;  (9) 89-10544.03, CORONARY BYPASS PACK PGYBK, Carilion Roanoke Memorial Hosp;  (10) 89-10545.02, CMC CRANIOTOMY PACK, Carilion Roanoke Memorial Hospital;  (11) 89-10552.02, CMC EXTREMITY PACK, Carilion Roanoke Memorial Hospital;  (12) 89-10553.02, CMC GYN LAPAROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (13) 89-10554.02, CMC GYN MAJOR PACK, Carilion Roanoke Memorial  Hospital;  (14) 89-10555.02, ORTHO MAJOR PACK, Carilion Roanoke Memorial Hospital;  (15) 89-10556.02, CMC HYSTEROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (16) 89-10558.04, CCASC LAPAROTOMY PACK, Carilion Roanoke Memorial Hospital;  (17) 89-10560.03, CMC LAPAROTOMY PACK, Carilion Roanoke Memorial Hospital;  (18) 89-10561.02, CMC LAPAROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (19) 89-10562.02, CMC MINOR ENT/PLASTIC PACK, Carilion Roanoke Memorial Hospital;  (20) 89-10564.02, CMC MAJOR PLASTIC PACK, Carilion Roanoke Memorial Hospital;  (21) 89-10569.02, CMC PEDIATRIC PACK, Carilion Roanoke Memorial Hospital;  (22) 89-10570.02, CMC POSTERIOR SPINE PACK, Carilion Roanoke Memorial Hospital;  (23) 89-10574.02, CMC SHOULDER ARTHROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (24) 89-10575.02, OWEN HIP PACK, Carilion Roanoke Memorial Hosp;  (25) 89-10576.03, THORACOSCOPY / THORACOTOMY, Carilion Roanoke Memorial Hosp;  (26) 89-10580.03, VALVE REPLACEMENT PACK PGYBK, Carilion Roanoke Memorial Hosp. (Devices, Class II). The enforcement record is RECORDED; the classification is a DETERMINATION (FDA's regulatory verdict); the boundary is INTERPRETATION (a recall ≠ harm to a specific person). Source: openFDA. CC0.",
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    "name": "Sterile custom surgical procedure packs:    (1) 89-10507.02, TOTAL KNEE PACK, Stonewall Jackson Hospital;  (2) 89-10508.02, LOCAL PACK, Stonewall Jackson Hospital;  (3) 89-10509.02, LAPAROTOMY PACK, Stonewall Jackson Hospital;  (4) 89-10517.04, CNRV BASIC SETUP PACK, New River Valley Medical Center;  (5) 89-10526.04, CNRV LAPAROSCOPY PACK, New River Valley Medical Center;  (6) 89-10530.04, CNRV PERIPHERAL VAS PACK, New River Valley Medical Center;  (7) 89-10532.04, CNRV SPINE PACK, New River Valley Medical Center;  (8) 89-10534.02, CMC ANTERIOR SPINE PACK, Carilion Roanoke Memorial Hosp;  (9) 89-10544.03, CORONARY BYPASS PACK PGYBK, Carilion Roanoke Memorial Hosp;  (10) 89-10545.02, CMC CRANIOTOMY PACK, Carilion Roanoke Memorial Hospital;  (11) 89-10552.02, CMC EXTREMITY PACK, Carilion Roanoke Memorial Hospital;  (12) 89-10553.02, CMC GYN LAPAROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (13) 89-10554.02, CMC GYN MAJOR PACK, Carilion Roanoke Memorial  Hospital;  (14) 89-10555.02, ORTHO MAJOR PACK, Carilion Roanoke Memorial Hospital;  (15) 89-10556.02, CMC HYSTEROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (16) 89-10558.04, CCASC LAPAROTOMY PACK, Carilion Roanoke Memorial Hospital;  (17) 89-10560.03, CMC LAPAROTOMY PACK, Carilion Roanoke Memorial Hospital;  (18) 89-10561.02, CMC LAPAROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (19) 89-10562.02, CMC MINOR ENT/PLASTIC PACK, Carilion Roanoke Memorial Hospital;  (20) 89-10564.02, CMC MAJOR PLASTIC PACK, Carilion Roanoke Memorial Hospital;  (21) 89-10569.02, CMC PEDIATRIC PACK, Carilion Roanoke Memorial Hospital;  (22) 89-10570.02, CMC POSTERIOR SPINE PACK, Carilion Roanoke Memorial Hospital;  (23) 89-10574.02, CMC SHOULDER ARTHROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (24) 89-10575.02, OWEN HIP PACK, Carilion Roanoke Memorial Hosp;  (25) 89-10576.03, THORACOSCOPY / THORACOTOMY, Carilion Roanoke Memorial Hosp;  (26) 89-10580.03, VALVE REPLACEMENT PACK PGYBK, Carilion Roanoke Memorial Hosp.",
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      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1691-2023/enforcement-record",
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      "name": "FDA recall Z-1691-2023: DeRoyal Industries Inc is recalling Sterile custom surgical procedure packs:    (1) 89-10507.02, TOTAL KNEE PACK, Stonewall Jackson Hospital;  (2) 89-10508.02, LOCAL PACK, Stonewall Jackson Hospital;  (3) 89-10509.02, LAPAROTOMY PACK, Stonewall Jackson Hospital;  (4) 89-10517.04, CNRV BASIC SETUP PACK, New River Valley Medical Center;  (5) 89-10526.04, CNRV LAPAROSCOPY PACK, New River Valley Medical Center;  (6) 89-10530.04, CNRV PERIPHERAL VAS PACK, New River Valley Medical Center;  (7) 89-10532.04, CNRV SPINE PACK, New River Valley Medical Center;  (8) 89-10534.02, CMC ANTERIOR SPINE PACK, Carilion Roanoke Memorial Hosp;  (9) 89-10544.03, CORONARY BYPASS PACK PGYBK, Carilion Roanoke Memorial Hosp;  (10) 89-10545.02, CMC CRANIOTOMY PACK, Carilion Roanoke Memorial Hospital;  (11) 89-10552.02, CMC EXTREMITY PACK, Carilion Roanoke Memorial Hospital;  (12) 89-10553.02, CMC GYN LAPAROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (13) 89-10554.02, CMC GYN MAJOR PACK, Carilion Roanoke Memorial  Hospital;  (14) 89-10555.02, ORTHO MAJOR PACK, Carilion Roanoke Memorial Hospital;  (15) 89-10556.02, CMC HYSTEROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (16) 89-10558.04, CCASC LAPAROTOMY PACK, Carilion Roanoke Memorial Hospital;  (17) 89-10560.03, CMC LAPAROTOMY PACK, Carilion Roanoke Memorial Hospital;  (18) 89-10561.02, CMC LAPAROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (19) 89-10562.02, CMC MINOR ENT/PLASTIC PACK, Carilion Roanoke Memorial Hospital;  (20) 89-10564.02, CMC MAJOR PLASTIC PACK, Carilion Roanoke Memorial Hospital;  (21) 89-10569.02, CMC PEDIATRIC PACK, Carilion Roanoke Memorial Hospital;  (22) 89-10570.02, CMC POSTERIOR SPINE PACK, Carilion Roanoke Memorial Hospital;  (23) 89-10574.02, CMC SHOULDER ARTHROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (24) 89-10575.02, OWEN HIP PACK, Carilion Roanoke Memorial Hosp;  (25) 89-10576.03, THORACOSCOPY / THORACOTOMY, Carilion Roanoke Memorial Hosp;  (26) 89-10580.03, VALVE REPLACEMENT PACK PGYBK, Carilion Roanoke Memorial Hosp.",
      "text": "The FDA logged enforcement record Z-1691-2023: DeRoyal Industries Inc is voluntarily recalling Sterile custom surgical procedure packs:    (1) 89-10507.02, TOTAL KNEE PACK, Stonewall Jackson Hospital;  (2) 89-10508.02, LOCAL PACK, Stonewall Jackson Hospital;  (3) 89-10509.02, LAPAROTOMY PACK, Stonewall Jackson Hospital;  (4) 89-10517.04, CNRV BASIC SETUP PACK, New River Valley Medical Center;  (5) 89-10526.04, CNRV LAPAROSCOPY PACK, New River Valley Medical Center;  (6) 89-10530.04, CNRV PERIPHERAL VAS PACK, New River Valley Medical Center;  (7) 89-10532.04, CNRV SPINE PACK, New River Valley Medical Center;  (8) 89-10534.02, CMC ANTERIOR SPINE PACK, Carilion Roanoke Memorial Hosp;  (9) 89-10544.03, CORONARY BYPASS PACK PGYBK, Carilion Roanoke Memorial Hosp;  (10) 89-10545.02, CMC CRANIOTOMY PACK, Carilion Roanoke Memorial Hospital;  (11) 89-10552.02, CMC EXTREMITY PACK, Carilion Roanoke Memorial Hospital;  (12) 89-10553.02, CMC GYN LAPAROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (13) 89-10554.02, CMC GYN MAJOR PACK, Carilion Roanoke Memorial  Hospital;  (14) 89-10555.02, ORTHO MAJOR PACK, Carilion Roanoke Memorial Hospital;  (15) 89-10556.02, CMC HYSTEROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (16) 89-10558.04, CCASC LAPAROTOMY PACK, Carilion Roanoke Memorial Hospital;  (17) 89-10560.03, CMC LAPAROTOMY PACK, Carilion Roanoke Memorial Hospital;  (18) 89-10561.02, CMC LAPAROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (19) 89-10562.02, CMC MINOR ENT/PLASTIC PACK, Carilion Roanoke Memorial Hospital;  (20) 89-10564.02, CMC MAJOR PLASTIC PACK, Carilion Roanoke Memorial Hospital;  (21) 89-10569.02, CMC PEDIATRIC PACK, Carilion Roanoke Memorial Hospital;  (22) 89-10570.02, CMC POSTERIOR SPINE PACK, Carilion Roanoke Memorial Hospital;  (23) 89-10574.02, CMC SHOULDER ARTHROSCOPY PACK, Carilion Roanoke Memorial Hospital;  (24) 89-10575.02, OWEN HIP PACK, Carilion Roanoke Memorial Hosp;  (25) 89-10576.03, THORACOSCOPY / THORACOTOMY, Carilion Roanoke Memorial Hosp;  (26) 89-10580.03, VALVE REPLACEMENT PACK PGYBK, Carilion Roanoke Memorial Hosp. — reason: The custom procedure packs contain light handle covers that have been recalled by another firm.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-04-17. Affected lots/codes: (1) 89-10507.02 - lot 58700464,  exp 12/1/2024, GTIN pack-00749756362788, case-50749756362783; (2) 89-10508.02 - lot 58700430, exp 9/1/2026, GTIN pack-00749756362818, case-50749756362813; (3) 89-10509.02 - lot 58775010, exp 12/1/2024, GTIN pack-00749756362832, case-50749756362837; (4) 89-10517.04 - lot 58700579, exp 12/1/2024, GTIN pack-00749756363228, case-50749756363223; (5) 89-10526.04 - lot 58388765, exp 11/1/2024, GTIN pack-00749756363242, case-50749756363247; (6) 89-10530.04 - lot 58543121, exp 11/1/2024, GTIN pack-00749756364447, case-50749756364442; (7) 89-10532.04 - lot 58543905, exp 7/1/2024, GTIN pack-00749756363266, case-50749756363261; (8) 89-10534.02 - lots 58565821 and 58700561, exp 3/1/2024, GTIN pack-00749756363532, case-50749756363537; (9) 89-10544.03 - lot 58700000, exp 10/1/2024, GTIN pack-00749756366342, case-50749756366347; (10) 89-10545.02 - lot 58565830, exp 3/1/2024, GTIN pack-00749756363556, case-50749756363551; (11) 89-10552.02 - lot 58700667, 58700675, and 58724108, exp 12/1/2024, GTIN pack-00749756363549, case-50749756363544; (12) 89-10553.02 - lot 58544060, exp 11/1/2024, GTIN pack-00749756363624, case-50749756363629; (13) 89-10554.02 - lot 58544166, exp 12/1/2024, GTIN pack-00749756363440, case-50749756363445; (14) 89-10555.02 - lot 58589647 and 58724116, exp 12/1/2024, GTIN pack-00749756363648, case-50749756363643; (15) 89-10556.02 - lot 58589567, exp 12/1/2024, GTIN pack-00749756364287, case-50749756364282; (16) 89-10558.04 - lot 58542769, exp 11/1/2024, lot 58621694 and 58699993, exp 12/1/2024, GTIN pack-00749756364430, case-50749756364435; (17) 89-10560.03 - lot 58543201, 58554436, and 58700499, exp 9/1/2024, GTIN pack-00749756363778, case-50749756363773; (18) 89-10561.02 - lot 58542793, exp 11/1/2024, lot 58589591 and 58738016, exp 12/1/2024, GTIN pack-00749756363723, case-50749756363728; (19) 89-10562.02 - lot 58621820, exp 10/1/2024, GTIN pack-00749756364140, case-50749756364145; (20) 89-10564.02 - lot 58543083, exp 11/1/2024, and lot 58700501, exp 12/1/2024, GTIN pack-00749756363761, case-50749756363766; (21) 89-10569.02 - lot 58544182 exp 12/1/2024, GTIN pack-00749756363457, case-50749756363452; (22) 89-10570.02 - lot 58700739, exp 1/1/2024, and 58775036, exp 3/14/2024, GTIN pack-00749756363587, case-50749756363582; (23) 89-10574.02 - lot 58700641, exp 7/1/2024, GTIN pack-00749756364041, case-50749756364046; (24) 89-10575.02 - lot 58565848, exp 12/1/2023, GTIN pack-00749756366144, case-50749756366149; (25) 89-10576.03 - lot 58700704, exp 12/1/2024, GTIN pack-00749756364126, case-50749756364121; (26) 89-10580.03 - lot 58543454, exp 8/1/2024, GTIN pack-00749756366328, case-50749756366323.. A RECORDED FDA enforcement action (occurred=true).",
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        "value": "Devices recall, status Ongoing",
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          "name": "openFDA drug & device enforcement (recall) reports — U.S. FDA",
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      "falsifier": "A RECORD of measured/reported events (occurred=true) from openFDA drug & device enforcement (recall) reports — U.S. FDA; superseded when openFDA drug & device enforcement (recall) reports — U.S. FDA publishes its next release."
    },
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      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1691-2023/fda-classification",
      "@type": "schema:Claim",
      "name": "FDA classified recall Z-1691-2023 as Class II",
      "text": "The FDA assigned this recall Class II: Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.. This is the FDA's official risk classification — its regulatory DETERMINATION of the hazard category (a verdict constituted by the FDA's recognition, occurred=FALSE), adjudged=TRUE because the FDA issued it. It is NOT a measurement of harm to any specific person.",
      "claimType": "regulatory_determination",
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        "source": "U.S. FDA recall classification (openFDA enforcement)",
        "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1691-2023&lang=eng",
        "value": "Class II",
        "adjudicator": {
          "name": "U.S. FDA recall classification (openFDA enforcement)",
          "url": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1691-2023&lang=eng"
        }
      },
      "falsifier": "occurred=FALSE: a regulatory DETERMINATION (an authority's classification/judgment) has NO material truthmaker independent of recognition — it is constituted by U.S. FDA recall classification (openFDA enforcement)'s say-so (a Searle institutional fact), not measured. adjudged=TRUE because U.S. FDA recall classification (openFDA enforcement) (an external authority) issued it. Distinct from a recorded measurement (which has an independent truthmaker) and from a modeled figure (a computed quantity, not a verdict). Challengeable; superseded if the authority reclassifies."
    },
    {
      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1691-2023/boundary",
      "@type": "schema:Claim",
      "name": "What an FDA recall is — and is NOT",
      "text": "A recall is a RECORDED FDA enforcement action — the FDA logged that a firm is removing or correcting a product, classed by the FDA's risk judgment. It does NOT establish that any specific unit is affected or caused harm; causation is not established. This record informs and compares — it is NOT medical advice and does not tell anyone to start or stop a drug or device. For a medical decision, route to the FDA recall record and a licensed pharmacist or prescriber.",
      "claimType": "interpretation",
      "reviewStatus": "current",
      "commercialInfluence": false,
      "epistemicStatus": {
        "occurred": false,
        "supported": true,
        "adjudged": false,
        "operative": true
      },
      "grounding": {
        "groundingType": "Interpretation",
        "source": "Atlas Commons L5 boundary (enforcement-action ≠ harm causation)",
        "sourceUrl": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/",
        "value": "a recorded enforcement action, not proof of harm or causation; not medical advice",
        "adjudicator": null
      },
      "falsifier": "occurred=FALSE (a framing, not an event) and adjudged=FALSE (an in-house reading, not an authority's verdict) — the LOWEST-warrant claim here. A flat representation would render this identically to the official facts; the four-status does not."
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          "item": {
            "Field": "Lot/code info",
            "Value": "(1) 89-10507.02 - lot 58700464,  exp 12/1/2024, GTIN pack-00749756362788, case-50749756362783; (2) 89-10508.02 - lot 58700430, exp 9/1/2026, GTIN pack-00749756362818, case-50749756362813; (3) 89-10509.02 - lot 58775010, exp 12/1/2024, GTIN pack-00749756362832, case-50749756362837; (4) 89-10517.04 - lot 58700579, exp 12/1/2024, GTIN pack-00749756363228, case-50749756363223; (5) 89-10526.04 - lot 58388765, exp 11/1/2024, GTIN pack-00749756363242, case-50749756363247; (6) 89-10530.04 - lot 58543121, exp 11/1/2024, GTIN pack-00749756364447, case-50749756364442; (7) 89-10532.04 - lot 58543905, exp 7/1/2024, GTIN pack-00749756363266, case-50749756363261; (8) 89-10534.02 - lots 58565821 and 58700561, exp 3/1/2024, GTIN pack-00749756363532, case-50749756363537; (9) 89-10544.03 - lot 58700000, exp 10/1/2024, GTIN pack-00749756366342, case-50749756366347; (10) 89-10545.02 - lot 58565830, exp 3/1/2024, GTIN pack-00749756363556, case-50749756363551; (11) 89-10552.02 - lot 58700667, 58700675, and 58724108, exp 12/1/2024, GTIN pack-00749756363549, case-50749756363544; (12) 89-10553.02 - lot 58544060, exp 11/1/2024, GTIN pack-00749756363624, case-50749756363629; (13) 89-10554.02 - lot 58544166, exp 12/1/2024, GTIN pack-00749756363440, case-50749756363445; (14) 89-10555.02 - lot 58589647 and 58724116, exp 12/1/2024, GTIN pack-00749756363648, case-50749756363643; (15) 89-10556.02 - lot 58589567, exp 12/1/2024, GTIN pack-00749756364287, case-50749756364282; (16) 89-10558.04 - lot 58542769, exp 11/1/2024, lot 58621694 and 58699993, exp 12/1/2024, GTIN pack-00749756364430, case-50749756364435; (17) 89-10560.03 - lot 58543201, 58554436, and 58700499, exp 9/1/2024, GTIN pack-00749756363778, case-50749756363773; (18) 89-10561.02 - lot 58542793, exp 11/1/2024, lot 58589591 and 58738016, exp 12/1/2024, GTIN pack-00749756363723, case-50749756363728; (19) 89-10562.02 - lot 58621820, exp 10/1/2024, GTIN pack-00749756364140, case-50749756364145; (20) 89-10564.02 - lot 58543083, exp 11/1/2024, and lot 58700501, exp 12/1/2024, GTIN pack-00749756363761, case-50749756363766; (21) 89-10569.02 - lot 58544182 exp 12/1/2024, GTIN pack-00749756363457, case-50749756363452; (22) 89-10570.02 - lot 58700739, exp 1/1/2024, and 58775036, exp 3/14/2024, GTIN pack-00749756363587, case-50749756363582; (23) 89-10574.02 - lot 58700641, exp 7/1/2024, GTIN pack-00749756364041, case-50749756364046; (24) 89-10575.02 - lot 58565848, exp 12/1/2023, GTIN pack-00749756366144, case-50749756366149; (25) 89-10576.03 - lot 58700704, exp 12/1/2024, GTIN pack-00749756364126, case-50749756364121; (26) 89-10580.03 - lot 58543454, exp 8/1/2024, GTIN pack-00749756366328, case-50749756366323.",
            "Status": "recorded"
          }
        },
        {
          "@type": "schema:ListItem",
          "position": 9,
          "item": {
            "Field": "Distribution pattern",
            "Value": "US Nationwide distribution in the state of VA.",
            "Status": "recorded"
          }
        }
      ]
    }
  ]
}