FDA Device recall Z-1577-2013
BD SafetyGlide Allergy
- FDA Device
- Class II
- terminated
- Published 2013-07-03
On 2013-07-03 the FDA classified a Class II recall of BD SafetyGlide Allergy by Becton Dickinson And, citing there has been an increase in complaints regarding the needle/safety mechanism disengaging from the syringe.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1577-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-01 |
| Published | 2013-07-03 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
BD SafetyGlide Allergy. REF 305950 Sterile Allergy Treatment Syringe Tray. The device is used for aspiration and injection of medications.
Reason
There has been an increase in complaints regarding the needle/safety mechanism disengaging from the syringe.
Identifiers
| code_info | Catalog/Lot Number: REF#305950 Lot 2132028 and Lot 2159189 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1577-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.