FDA Medical Device Recalls (openFDA)
Becton Dickinson & Company: ReliOn Insulin Syringe 0.5cc 30 Gauge 5/16 inch (8mm) Needle (U-100 Insulin). NDC 81306-0515-23.
- Recall number
- Z-0569-05
- Recalling firm
- Becton Dickinson & Company
- Product
- ReliOn Insulin Syringe 0.5cc 30 Gauge 5/16 inch (8mm) Needle (U-100 Insulin). NDC 81306-0515-23.
- Status
- Terminated
- Initiated
- 2004-10-22
- Posted
- 2005-03-03
- Terminated
- 2006-04-14
- Reason
- Syringes labeled as 5/16 inch product (30 ga) actually contained the 1/2 inch product (28 ga).
- Root cause
- Other
- Action
- BD has sent letters to the distributor McKesson Inc and the retailer Wal-Mart Inc.
- Quantity
- 1543000 syringes
- Distribution
- The syringes were sent to McKesson Corp, 120 Senlac Drive, Carrollton, TX 75006 who then sold them to Wal-Mart Corp, 702 SW 8th Street, Bentonville, AR 72716. There are no other customers.
- Lot, serial or model codes
- Batch # 4083690
- 510(k) numbers
- ["K955235"]
- PMA numbers
- not on file
- Product code
- FMF
- 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