FDA Medical Device Recalls (openFDA)
Becton Dickinson & Company: 3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061
- Recall number
- Z-2008-2019
- Recalling firm
- Becton Dickinson & Company
- Product
- 3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061
- Status
- Terminated
- Initiated
- 2019-02-01
- Posted
- not on file
- Terminated
- 2020-06-11
- Reason
- The syringes have scale markings that were printed incorrectly. The scale is skewed to varying degrees, resulting in missing and/or partially printed scale numbers and scale lines.
- Root cause
- Under Investigation by firm
- Action
- Urgent Medical Device Recall notification letters dated 2/1/19 were sent to customers.
- Quantity
- 428,800
- Distribution
- The products were distributed to the following US states: FL, IL, KS, MA, ND, NH, NY, OH, PA, RI, SC, VA, and WI. The products were distributed to the following foreign countries: Suriname.
- Lot, serial or model codes
- Lot Number 8307694
- 510(k) numbers
- ["K944757"]
- 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