{ "@context": { "schema": "https://schema.org/", "au": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/vocab/agent-native#", "@vocab": "https://schema.org/", "claims": { "@id": "au:claims", "@container": "@list" }, "epistemicStatus": "au:epistemicStatus", "occurred": "au:occurred", "supported": "au:supported", "adjudged": "au:adjudged", "operative": "au:operative", "grounding": "au:grounding", "groundingType": "au:groundingType", "adjudicator": "au:adjudicator", "source": "au:source", "sourceUrl": "au:sourceUrl", "value": "au:value", "claimType": "au:claimType", "reviewStatus": "au:reviewStatus", "commercialInfluence": "au:commercialInfluence", "falsifier": "au:falsifier" }, "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0466-2026.jsonld", "@type": "schema:Dataset", "name": "Radiography 7300 C; Model Number: 712037;", "description": "FDA recall Z-0466-2026 — Philips Medical Systems DMC GmbH is recalling Radiography 7300 C; Model Number: 712037; (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.", "license": "https://creativecommons.org/publicdomain/zero/1.0/", "isAccessibleForFree": true, "isPartOf": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/", "rdfs:isDefinedBy": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/vocab/agent-native", "seeAlso": "https://agenticu.ryanjhunter.workers.dev/commons/the-research-object", "dateModified": "2026-06-24T07:02:03.626072+00:00", "isBasedOn": { "@type": "schema:Dataset", "name": "openFDA drug & device enforcement (recall) reports", "url": "https://open.fda.gov/apis/drug/enforcement/", "creator": { "@type": "schema:GovernmentOrganization", "name": "U.S. Food & Drug Administration" } }, "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-0466-2026&lang=eng", "about": { "@type": "schema:MedicalDevice", "name": "Radiography 7300 C; Model Number: 712037;", "manufacturer": { "@type": "schema:Organization", "name": "Philips Medical Systems DMC GmbH" } }, "claims": [ { "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0466-2026/enforcement-record", "@type": "schema:Claim", "name": "FDA recall Z-0466-2026: Philips Medical Systems DMC GmbH is recalling Radiography 7300 C; Model Number: 712037;", "text": "The FDA logged enforcement record Z-0466-2026: Philips Medical Systems DMC GmbH is voluntarily recalling Radiography 7300 C; Model Number: 712037; — reason: Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.. Status: Ongoing — the recall is still being carried out.. Initiated 2025-10-01. Affected lots/codes: Model Number: 712037; UDI-DI: 00884838116016; Serial Numbers: 6, 7, 8, 9, 11, 12, 13, 14, 15, 17, 24860004, 24860006, 24860008, 24860009, 24860010, 24860011, 24860012, 24860013, 24860014, 24860015, 24860017, 24860018, 24860019, 24860021, 24860034, 24860036, 24860037, 24860038, 24860039, 24860040, 24860044, 24860045, 24860047, 24860049, 24860051, 24860053, 24860055, 24860056, 24860057, 24860058, 24860059, 24860060, 24860061, 24860062, 24860064, 24860065, 24860066, 24860067, 24860068, 24860069, 24860070, 24860072, 24860073, 24860074, 24860075, 24860076, 24860077, 24860078, 24860079, 24860080, 24860081, 24860082, 24860083, 24860084, 24860085, 24860086, 24860087, 24860088, 24860089, 24860090, 24860091, 24860092, 24860093, 24860094, 24860096, 24860098, 24860099, 24860100, 24860101, 24860102, 24860103, 24860104, 24860105, 24860106, 24860107, 24860108, 24860109, 24860110, 24860111, 24860112, 24860113, 24860115, 24860116, 24860117, 24860118, 24860119, 24860120, 24860121, 24860122, 24860123, 24860124, 24860125, 24860126, 24860128, 24860129, 24860130, 24860131, 24860133, 24860135, 24860137, 24860139, 24860141, 24860142, 24860143, 24860144, 24860145, 24860146, 24860148, 24860149, 24860150, 24860153, 24860157, 24860158, 24860159, 24860163, 24860164, 24860165, 24860166, 24860167, 24860168, 24860169, 24860170, 24860172, 24860173, 24860174, 24860175, 24860177, 24860178, 24860179, 24860180, 24860181, 24860182, 24860183, 24860184, 24860185, 24860186, 24860187, 24860191, 24860192, 24860193, 24860196, 24860197, 24860198, 24860200, 24860203, 24860204, 24860205, 24860207, 24860208, 24860209, 24860210, 24860211, 24860212, 24860213, 24860214, 24860216, 24860217, 24860218, 24860219, 24860220, 24860221, 24860222, 24860223, 24860224, 24860225, 24860226, 24860227, 24860228, 24860229, 24860232, 24860233, 24860234, 24860235, 24860236, 24860237, 24860238, 24860239, 24860240, 24860241, 24860248, 24860252, 24860254, 24860255, 24860256, 24860257, 24860259, 24860260, 24860261, 24860262, 24860264, 24860265, 24860266, 24860267, 24860268, 24860269, 24860270, 24860271, 24860272, 24860273, 24860275, 24860276, 24860277, 24860278, 24860280, 24860281, 24860282, 24860283, 24860284, 24860286, 24860288, 24860289, 24860290, 24860294, 24860295, 24860296, 24860297, 24860298, 24860299, 24860302, 24860306, 24860308, 24860310, 24860311, 24860312, 24860314, 24860315, 24860317, 24860318, 24860319, 24860321, 24860322, 24860324, 24860325, 24860328, 24860332, 24860337, 24860338, 24860339, 24860340, 24860342, 24860343, 24860344, 24860352, 24860355, 24860356, 24860357, 24860361, 24860363, 24860365, 24860366, 24860367, 24860368, 24860369, 24860370, 24860372, 24860373, 24860376, 24860382, 24860383, 24860384, 24860388, 24860390, 24860391, 24860392, 24860393, 24860394, 24860401, 24860404, 24860407, 24860410, 24860411, 24860416, 24860420, 24860425;. A RECORDED FDA enforcement action (occurred=true).", "claimType": "official_fact", "reviewStatus": "current", "commercialInfluence": false, "epistemicStatus": { "occurred": true, "supported": true, "adjudged": true, "operative": true }, "grounding": { "groundingType": "SourceCitation", "source": "openFDA drug & device enforcement (recall) reports — U.S. FDA", "sourceUrl": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-0466-2026&lang=eng", "value": "Devices recall, status Ongoing", "adjudicator": { "name": "openFDA drug & device enforcement (recall) reports — U.S. FDA", "url": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-0466-2026&lang=eng" } }, "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." }, { "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-0466-2026/fda-classification", "@type": "schema:Claim", "name": "FDA classified recall Z-0466-2026 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", "reviewStatus": "current", "commercialInfluence": false, "epistemicStatus": { "occurred": false, "supported": true, "adjudged": true, "operative": true }, "grounding": { "groundingType": "AdjudicativeAct", "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-0466-2026&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-0466-2026&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-0466-2026/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." } ], "hasPart": [ { "@type": "schema:ItemList", "name": "FDA recall details — Z-0466-2026", "numberOfItems": 9, "itemListElement": [ { "@type": "schema:ListItem", "position": 1, "item": { "Field": "Recall number", "Value": "Z-0466-2026", "Status": "recorded" } }, { "@type": "schema:ListItem", "position": 2, "item": { "Field": "Product type", "Value": "Devices", "Status": "recorded" } }, { "@type": "schema:ListItem", "position": 3, "item": { "Field": "Classification", "Value": "Class II", "Status": "determination" } }, { "@type": "schema:ListItem", "position": 4, "item": { "Field": "Status", "Value": "Ongoing — the recall is still being carried out.", "Status": "recorded" } }, { "@type": "schema:ListItem", "position": 5, "item": { "Field": "Recalling firm", "Value": "Philips Medical Systems DMC GmbH", "Status": "recorded" } }, { "@type": "schema:ListItem", "position": 6, "item": { "Field": "Reason", "Value": "Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.", "Status": "recorded" } }, { "@type": "schema:ListItem", "position": 7, "item": { "Field": "Initiated", "Value": "2025-10-01", "Status": "recorded" } }, { "@type": "schema:ListItem", "position": 8, "item": { "Field": "Lot/code info", "Value": "Model Number: 712037; UDI-DI: 00884838116016; Serial Numbers: 6, 7, 8, 9, 11, 12, 13, 14, 15, 17, 24860004, 24860006, 24860008, 24860009, 24860010, 24860011, 24860012, 24860013, 24860014, 24860015, 24860017, 24860018, 24860019, 24860021, 24860034, 24860036, 24860037, 24860038, 24860039, 24860040, 24860044, 24860045, 24860047, 24860049, 24860051, 24860053, 24860055, 24860056, 24860057, 24860058, 24860059, 24860060, 24860061, 24860062, 24860064, 24860065, 24860066, 24860067, 24860068, 24860069, 24860070, 24860072, 24860073, 24860074, 24860075, 24860076, 24860077, 24860078, 24860079, 24860080, 24860081, 24860082, 24860083, 24860084, 24860085, 24860086, 24860087, 24860088, 24860089, 24860090, 24860091, 24860092, 24860093, 24860094, 24860096, 24860098, 24860099, 24860100, 24860101, 24860102, 24860103, 24860104, 24860105, 24860106, 24860107, 24860108, 24860109, 24860110, 24860111, 24860112, 24860113, 24860115, 24860116, 24860117, 24860118, 24860119, 24860120, 24860121, 24860122, 24860123, 24860124, 24860125, 24860126, 24860128, 24860129, 24860130, 24860131, 24860133, 24860135, 24860137, 24860139, 24860141, 24860142, 24860143, 24860144, 24860145, 24860146, 24860148, 24860149, 24860150, 24860153, 24860157, 24860158, 24860159, 24860163, 24860164, 24860165, 24860166, 24860167, 24860168, 24860169, 24860170, 24860172, 24860173, 24860174, 24860175, 24860177, 24860178, 24860179, 24860180, 24860181, 24860182, 24860183, 24860184, 24860185, 24860186, 24860187, 24860191, 24860192, 24860193, 24860196, 24860197, 24860198, 24860200, 24860203, 24860204, 24860205, 24860207, 24860208, 24860209, 24860210, 24860211, 24860212, 24860213, 24860214, 24860216, 24860217, 24860218, 24860219, 24860220, 24860221, 24860222, 24860223, 24860224, 24860225, 24860226, 24860227, 24860228, 24860229, 24860232, 24860233, 24860234, 24860235, 24860236, 24860237, 24860238, 24860239, 24860240, 24860241, 24860248, 24860252, 24860254, 24860255, 24860256, 24860257, 24860259, 24860260, 24860261, 24860262, 24860264, 24860265, 24860266, 24860267, 24860268, 24860269, 24860270, 24860271, 24860272, 24860273, 24860275, 24860276, 24860277, 24860278, 24860280, 24860281, 24860282, 24860283, 24860284, 24860286, 24860288, 24860289, 24860290, 24860294, 24860295, 24860296, 24860297, 24860298, 24860299, 24860302, 24860306, 24860308, 24860310, 24860311, 24860312, 24860314, 24860315, 24860317, 24860318, 24860319, 24860321, 24860322, 24860324, 24860325, 24860328, 24860332, 24860337, 24860338, 24860339, 24860340, 24860342, 24860343, 24860344, 24860352, 24860355, 24860356, 24860357, 24860361, 24860363, 24860365, 24860366, 24860367, 24860368, 24860369, 24860370, 24860372, 24860373, 24860376, 24860382, 24860383, 24860384, 24860388, 24860390, 24860391, 24860392, 24860393, 24860394, 24860401, 24860404, 24860407, 24860410, 24860411, 24860416, 24860420, 24860425;", "Status": "recorded" } }, { "@type": "schema:ListItem", "position": 9, "item": { "Field": "Distribution pattern", "Value": "Worldwide Distribution: US (Nationwide) Distribution and OUS (International) countries of: Australia, Austria, Bahrain, Belgium, Bosnia-Herz., Canada, Chile, Croatia, Denmark, Estonia, Finland, France, Germany, Ghana, Gibraltar, Guadeloupe, Indonesia, Iraq, Israel, Italy, Jordan, Kuwait, Kyrgyzstan, Latvia, Lithuania, Netherlands, New Zealand, Norway, Panama, Philippines, Poland, Portugal, R¿union, Samoa, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, T¿rkiye, Turkmenistan, United Kingdom, Utd.Arab.Emir.,", "Status": "recorded" } } ] } ] }