CareFusion V — Class II medical device recall Z-0398-2023
Ongoing recall by Carefusion 2200 Inc, reported 2022-12-14, distributed nationwide. XXX
| Recall number | Z-0398-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Carefusion 2200 Inc, Vernon Hills, IL, United States |
| Recall initiated | 2022-11-02 |
| Classified | 2022-12-03 |
| Reported by FDA | 2022-12-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, CA, DE, EG, HK, IL, KR, PH, SA, TH, ZA |
| Quantity | 4 units |
| UPC / GTIN / UDI-DI | 10885403041013 |
| Model numbers | F-5008 |
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 0.7MM TIP OVERALL LENGTH 9-1/2" (240MM) , REF F-5008
Reason for recall
XXX
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-0398-2023. 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.