FDA Device recall Z-0630-2022
BD Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings
- FDA Device
- Class II
- ongoing
- Published 2022-02-16
On 2022-02-16 the FDA classified a Class II recall of BD Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings by Becton Dickinson And, citing 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 in….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0630-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-01-05 |
| Published | 2022-02-16 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
BD Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings. Catalog Number: 256066
Reason
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.
Identifiers
| code_info | All unexpired analyzers (Exp. Date 12/2021 - 8/2024) UDI: 00382902560661 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0630-2022%22
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