FDAMay 25, 2023device

Quidel Triage Cardiac Panel: REF: 97000HS, 97021HS (Troponin I), 97022HS (CK-MB and Troponin I), 97000HSEU, 97000HSEUJP, 97000HZ01, 97000QIL. Lots T13664 - T14045.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Raw material issue may cause cardiac panel products to have an average of 30% troponin signal reduction across measurement range 0.05 ng/mL to 30 ng/mL, QC testing won't detect anomaly, so an alternate method is recommended, if unavailable, use recommendations to mitigate potential patient impact, which could be missed/delayed myocardial infarction diagnosis.

What to do

FDA enforcement status: Ongoing

Brands named

quidel cardiovascularquidel

UPCs

30014613337911300146133379353001461333794230014613337928

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Quidel Triage Cardiac Panel: REF: 97000HS, 97021HS (Troponin I), 97022HS (CK-MB and Troponin I), 97000HSEU, 97000HSEUJP, 97000HZ01, 97000QIL. Lots T13664 - T14045. — Recall Details · AllClear