Data Foundry

Medical device recalls 2021

REF: 08P1820 — Class II medical device recall Z-2184-2021

Ongoing recall by Abbott Laboratories, reported 2021-08-11, distributed nationwide. There is a potential for 15% under-recovery on Activated Alanine Aminotransferase (A-ALT) samples greater than

Recall numberZ-2184-2021
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmAbbott Laboratories, Irving, TX, United States
Recall initiated2021-06-10
Classified2021-08-02
Reported by FDA2021-08-11
DistributedNationwide (US)
Countries outside the USAF, AT, AU, BD, BE, BS, CA, CH, CN, CZ, DE, DK, EG, ES, FI, FR, GB, HK, HR, IE, IL, IN, IT, KW, KY, LT, LU, MX, NL, NO, OM, PA, PH, PK, PT, RO, RU, SA, SE, SI, SK, TH, TT, VN
Quantity4,727 units
UPC / GTIN / UDI-DI00380740132569
Lot numbers01JAN2022, 02MAR2022, 03168UN20, 08JAN2022, 09237UN21, 09787UN20, 09APR2022, 09JUL2021, 24OCT2021, 25SEP2021, 37977UN20, 63000UN20, 77743UN21, 77745UN20, 83459UN20
Model numbers08P1820

Product

REF: 08P1820, Abbott Alinity c Activated Alanine Aminotransferase reagent Kit, Alinity c Activated Alanine Aminotransferase Reagent Kit,, IVD, CE, UDI: (01) 00380740132569

Reason for recall

There is a potential for 15% under-recovery on Activated Alanine Aminotransferase (A-ALT) samples greater than 1,200 U/L. In addition there is a potential for a >10% shift in patient results with samples containing bilirubin concentrations greater that 31 mg/dL. This could lead to incorrect patient results.

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-2184-2021. 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.