BD SafetyGlide Allergy — Class II medical device recall Z-1577-2013
Terminated recall by Becton Dickinson & Company, reported 2013-07-03, distributed nationwide. There has been an increase in complaints regarding the needle/safety mechanism disengaging from the syringe.
| Recall number | Z-1577-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2013-05-01 |
| Classified | 2013-06-21 |
| Reported by FDA | 2013-07-03 |
| Terminated | 2013-09-25 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 1,326,000 units |
| Lot numbers | 2132028, 2159189 |
| Model numbers | 305950 |
Product
BD SafetyGlide Allergy. REF 305950 Sterile Allergy Treatment Syringe Tray. The device is used for aspiration and injection of medications.
Reason for recall
There has been an increase in complaints regarding the needle/safety mechanism disengaging from the syringe.
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-1577-2013. 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.