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  "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1350-2023.jsonld",
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  "name": "Easy Read App associated with First Response Pregnancy Test Sticks  - Intended use of converting analog pregnancy test results into text  pregnant  or  not pregnant  for display on consumer devices (e.g., smart phone, iPad)",
  "description": "FDA recall Z-1350-2023 — Church & Dwight Inc is recalling Easy Read App associated with First Response Pregnancy Test Sticks  - Intended use of converting analog pregnancy test results into text  pregnant  or  not pregnant  for display on consumer devices (e.g., smart phone, iPad) (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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  "dateModified": "2026-06-24T07:02:03.626072+00:00",
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  "sameAs": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1350-2023&lang=eng",
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    "name": "Easy Read App associated with First Response Pregnancy Test Sticks  - Intended use of converting analog pregnancy test results into text  pregnant  or  not pregnant  for display on consumer devices (e.g., smart phone, iPad)",
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      "name": "Church & Dwight Inc"
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      "@id": "https://drug-device-safety-atlas.ryanjhunter.workers.dev/recalls/Z-1350-2023/enforcement-record",
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      "name": "FDA recall Z-1350-2023: Church & Dwight Inc is recalling Easy Read App associated with First Response Pregnancy Test Sticks  - Intended use of converting analog pregnancy test results into text  pregnant  or  not pregnant  for display on consumer devices (e.g., smart phone, iPad)",
      "text": "The FDA logged enforcement record Z-1350-2023: Church & Dwight Inc is voluntarily recalling Easy Read App associated with First Response Pregnancy Test Sticks  - Intended use of converting analog pregnancy test results into text  pregnant  or  not pregnant  for display on consumer devices (e.g., smart phone, iPad) — reason: Church & Dwight First Response Pregnancy Kits was marketed with the Easy Read App without a new 510k.  There is also a potential for Easy Read App to be unable to reads the test results (i.e., no results reported on the APP screen) or to misread the analog results shown on the pregnancy test stick and may lead to misinterpretation of false positive or false negative tests by the user.. Status: Ongoing — the recall is still being carried out.. Initiated 2023-01-25. Affected lots/codes: All lots with the Easy Read App. A RECORDED FDA enforcement action (occurred=true).",
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        "value": "Devices recall, status Ongoing",
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          "url": "https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1350-2023&lang=eng"
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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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      "name": "FDA classified recall Z-1350-2023 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.",
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      "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."
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    {
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      "@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",
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        "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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            "Field": "Reason",
            "Value": "Church & Dwight First Response Pregnancy Kits was marketed with the Easy Read App without a new 510k.  There is also a potential for Easy Read App to be unable to reads the test results (i.e., no results reported on the APP screen) or to misread the analog results shown on the pregnancy test stick and may lead to misinterpretation of false positive or false negative tests by the user.",
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          "item": {
            "Field": "Distribution pattern",
            "Value": "US Nationwide distribution.",
            "Status": "recorded"
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