Drug recall
BD Regional Block Needles 22G x 1.50in (50 units/cs.). Indicated for administration of medications to affect…
FDA recall event 86994 · Class II · Becton Dickinson & Company
Key facts
| Event ID | 86994 |
|---|---|
| Recall numbers | Z-0923-2021, Z-0924-2021 |
| Recalling firm | Becton Dickinson & Company |
| Product type | Devices |
| Products | BD Regional Block Needles 22G x 1.50in (50 units/cs.). Indicated for administration of medications to affect anesthesia or analgesia to a specific anatomical location (region). Catalog No. 408348, BD Stimex Insulated Needle 22G x 2.13in ( 50 units/cs.) Indicated for administration of medications to affect anesthesia or analgesia to a specific anatomical location (region). Catalog No. 404204 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | BD was advised by the European Notified Body, NSAI, that the instructions for use (IFU) needs to be updated to include the general contraindications |
| Initiation date | Dec 9, 2020 |
| Report date | Feb 3, 2021 |
| Termination date | Aug 10, 2022 |
| City | Franklin Lakes |
| State | NJ |
| Country | United States |
| FEI number | 2243072 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: