Class II — Becton Dickinson & Company
| Recalling firm | Becton Dickinson and Company |
|---|---|
| Registered facility | View this company's 36 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | There has been an increase in complaints regarding the needle/safety mechanism disengaging from the syringe. |
| Product | BD SafetyGlide Allergy. REF 305950 Sterile Allergy Treatment Syringe Tray. The device is used for aspiration and injection of medications. |
| Quantity | 1,326,000 units |
| Distribution | Worldwide Distribution including US Nationwide and the countries of Canada and Suriname. |
| Initiated | 2013-05-01 |
| Classified | 2013-06-21 |
| Terminated | 2013-09-25 |
| Recall number | Z-1577-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Becton Dickinson & Company (Z-1577-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/65243/
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