FDA Device recall Z-2007-2019
3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573
- FDA Device
- Class II
- terminated
- Published 2019-07-31
On 2019-07-31 the FDA classified a Class II recall of 3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573 by Becton Dickinson And, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2007-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-02-01 |
| Published | 2019-07-31 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | FL, IL, KS, MA, ND, NH, NY, OH, PA, RI, SC, VA, WI |
Product
3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573
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.
Identifiers
| code_info | Lot Number 8303571 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2007-2019%22
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