FDA Medical Device Recalls (openFDA)
Becton Dickinson & Company: BD SafetyGlide Allergy. REF 305950 Sterile Allergy Treatment Syringe Tray. The device is used for aspiration and injection of medications.
- Recall number
- Z-1577-2013
- Recalling firm
- Becton Dickinson & Company
- Product
- BD SafetyGlide Allergy. REF 305950 Sterile Allergy Treatment Syringe Tray. The device is used for aspiration and injection of medications.
- Status
- Terminated
- Initiated
- 2013-05-01
- Posted
- 2013-06-21
- Terminated
- 2013-09-25
- Reason
- There has been an increase in complaints regarding the needle/safety mechanism disengaging from the syringe.
- Root cause
- Process control
- Action
- Direct consignees were contacted by phone and email on 05/01/2013 and instructed to return the affected product. End users were mailed "Urgent: Product Recall" letters/Response Forms dated 05/01/2013. The notice advises customers of the product issue, identifies affected product and provides instructions on how to handle affected product.
- Quantity
- 1,326,000 units
- Distribution
- Worldwide Distribution including US Nationwide and the countries of Canada and Suriname.
- Lot, serial or model codes
- Catalog/Lot Number: REF#305950 Lot 2132028 and Lot 2159189
- 510(k) numbers
- ["K992734"]
- PMA numbers
- not on file
- Product code
- MEG
- Firm FEI
- 2243072
- Firm city
- Franklin Lakes
- Firm state
- NJ
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28