CareFusion V — Class II medical device recall Z-0414-2023
Ongoing recall by Carefusion 2200 Inc, reported 2022-12-14, distributed nationwide. BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contai
| Recall number | Z-0414-2023 |
|---|---|
| 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 | 147 units |
| UPC / GTIN / UDI-DI | 10885403041273 |
| Model numbers | F-5302 |
Product
CareFusion V. Mueller TITANIUM BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED STRAIGHT FINE, 0.5MM TIP OVERALL LENGTH 8-3/4" (225MM), REF F-5302
Reason for recall
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface with the device power supply, as well as cleaning and maintenance instructions. Refer to the attached V. Mueller" Bipolar Forcep IFU.
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-0414-2023. 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.