BD Veritor Plus Analyzer — Class II medical device recall Z-0630-2022
Ongoing recall by Becton Dickinson & Co., reported 2022-02-16, distributed nationwide. May have the potential to overheat and/or cause fire, the issue can occur when an unauthorized alternative AC
| Recall number | Z-0630-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Co., Sparks, MD, United States |
| Recall initiated | 2022-01-05 |
| Classified | 2022-02-09 |
| Reported by FDA | 2022-02-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BE, BR, CA, CL, CN, CO, DO, EC, GT, HK, HN, HT, ID, IN, JM, KR, MX, NZ, PA, PE, PH, SG, SV, TH, TT, TW, UY, VN |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00382902560661 |
| Model numbers | 256066 |
| Expiration dates | 2021-12 |
Product
BD Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings. Catalog Number: 256066
Reason for recall
May have the potential to overheat and/or cause fire, the issue can occur when an unauthorized alternative AC power adapter, and not the one provided by BD is used to power the instrument.
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-0630-2022. 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.