Data Foundry

Medical device recalls 2013

Clinical Chemistry Phosphorus Reagent The Phosphorus assay is used… — Class II medical device recall Z-0020-2014

Terminated recall by Abbott Laboratories, Inc, reported 2013-10-23, distributed nationwide. Reagent lots 64736UN12, 03991UN13, 51611UN13, 74805UN12, and 03992UN13 have incorrect expiration dates assigne

Recall numberZ-0020-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAbbott Laboratories, Inc, Irving, TX, United States
Recall initiated2013-08-12
Classified2013-10-17
Reported by FDA2013-10-23
Terminated2015-04-06
DistributedNationwide (US)
Countries outside the USAE, AR, AT, AU, BD, BE, BG, BR, BS, CA, CH, CL, CN, CW, CY, CZ, DE, DK, DO, DZ, EE, EG, ES, FI, FR, GB, GR, GT, HK, HR, IE, IL, IN, IQ, IT, JM, JO, KE, KR, KW, KY, LB, LT, LU, LV, MA, MX, MY, NL, NO, NZ, OM, PA, PH, PK, PL, PT, PY, QA, RO, RS, RU, SA, SE, SG, SI, SK, SV, TH, TN, TR, TT, TW, UY, VN, ZA
Quantity7,213
Reason classeslabeling
Lot numbers64736UN12, 74805UN12

Product

Clinical Chemistry Phosphorus Reagent The Phosphorus assay is used for the quantitation of phosphorus in human serum, plasma, or urine.

Reason for recall

Reagent lots 64736UN12, 03991UN13, 51611UN13, 74805UN12, and 03992UN13 have incorrect expiration dates assigned by Supplier.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0020-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.