Data Foundry

Medical device recalls 2024

In-vitro diagnostic kits: — Class III medical device recall Z-1189-2024

Ongoing recall by Abbott Molecular, Inc., reported 2024-03-06, distributed nationwide. Products that were intended for export only which were not approved or registered in accordance with U.S. spec

Recall numberZ-1189-2024
Product typeMedical device
ClassificationClass III
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmAbbott Molecular, Inc., Des Plaines, IL, United States
Recall initiated2024-02-01
Classified2024-02-26
Reported by FDA2024-03-06
DistributedNationwide (US)
Quantity7 kits
Reason classesunapproved product
UPC / GTIN / UDI-DI00884999000759, 00884999009301, 00884999009882, 00884999009912, 00884999010451
Lot numbers381102, 381111, 381411, 382133, 530242
Model numbers01N33-020, 04N62-020, 05J03-001, 05J03-004, 05J04-022
Expiration dates2024-03-28, 2024-05-25, 2024-06-17, 2024-09-22

Product

In-vitro diagnostic kits: (1) Abbott Vysis LSI ATM (11q22.3) SpectrmOrange Probe, REF 01N33-020; (2) Abbott Vysis PTEN/CEP 10 FISH Probe Kit, REF 04N62-020; (3) Abbott Vysis TelVysion 1p SpectrumGreen Probe, REF 05J03-001; (4) Abbott Vysis TelVysion 4P SpectrumGreen Probe, REF 05J03-004; (5) Abbott Vysis TelVysion 22q SpectrumOrange Probe, REF 05J04-022;

Reason for recall

Products that were intended for export only which were not approved or registered in accordance with U.S. specifications were shipped to U.S. customers.

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-1189-2024. 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.