cobas¿ Liat Influenza A/B Quality Control Kit — Class III medical device recall Z-2203-2016
Terminated recall by Roche Molecular Systems, Inc., reported 2016-07-20, distributed in AK, HI, IA, LA, MA, MD, ME, MN…. Kit labeled with the incorrect expiration date.
| Recall number | Z-2203-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Roche Molecular Systems, Inc., Branchburg, NJ, United States |
| Recall initiated | 2016-05-17 |
| Classified | 2016-07-13 |
| Reported by FDA | 2016-07-20 |
| Terminated | 2017-02-01 |
| Distributed | AK, HI, IA, LA, MA, MD, ME, MN, MT, NC, NY, OR, PA, TX, VA, WA |
| Quantity | 194 distributed |
| Reason classes | labeling |
| Lot numbers | 51222E, 60121H, 60201D, 60229F |
Product
cobas¿ Liat Influenza A/B Quality Control Kit; For use with cobas¿ Liat Influenza A/B Assay.
Reason for recall
Kit labeled with the incorrect expiration date.
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-2203-2016. 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.