FDA Medical Device Recalls (openFDA)
Becton Dickinson & Company: BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack
- Recall number
- Z-2889-2020
- Recalling firm
- Becton Dickinson & Company
- Product
- BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack
- Status
- Terminated
- Initiated
- 2020-07-28
- Posted
- not on file
- Terminated
- 2021-04-23
- Reason
- Printed scale markings on the 3mL SafetyGlide syringes, with catalog # 305924, Lot# 8289599, are printed incorrectly. The scale is skewed to different degrees, resulting in missing and/or partially printed scale numbers and scale lines.
- Root cause
- Equipment maintenance
- Action
- BD Sent a customer letter dated 28 July 2020. this letter requests customers to review their inventory for effected lots and Destroy all product subject to the recall. The letter requests customers to return the included response form and notify BD of any adverse events associated to this product.
- Quantity
- 125,200 units
- Distribution
- US and Canada
- Lot, serial or model codes
- Catalog #: 305924 Lot #: 8289599 UDI #: 30382903059240
- 510(k) numbers
- ["K951254"]
- PMA numbers
- not on file
- Product code
- FMI
- 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