Drug recall
BD Ultra-Fine Pen Needles 32G x 4mm (5/32')-intended for parenteral administration of a drug from a cartridge…
FDA recall event 86679 · Class II · Becton Dickinson & Company
Key facts
| Event ID | 86679 |
|---|---|
| Recall numbers | Z-0508-2021 |
| Recalling firm | Becton Dickinson & Company |
| Product type | Devices |
| Products | BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for parenteral administration of a drug from a cartridge contained in a drug pen injector Catalog Number: 320122 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product shelf cartons incorrectly labeled as products intended for the Latin American market. Although the product description on the label 32G x 4mm pen needles is correct, information pertinent to… |
| Initiation date | Oct 23, 2020 |
| Report date | Dec 9, 2020 |
| Termination date | Sep 8, 2023 |
| 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: