3mL Safety-Lok Syringe — Class II medical device recall Z-2008-2019
Terminated recall by Becton Dickinson & Company, reported 2019-07-31, distributed in FL, IL, KS, MA, ND, NH, NY, OH…. The syringes have scale markings that were printed incorrectly. The scale is skewed to varying degrees, result
| Recall number | Z-2008-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2019-02-01 |
| Classified | 2019-07-22 |
| Reported by FDA | 2019-07-31 |
| Terminated | 2020-06-11 |
| Distributed | FL, IL, KS, MA, ND, NH, NY, OH, PA, RI, SC, VA, WI |
| Quantity | 428,800 |
| UPC / GTIN / UDI-DI | 30382903096061 |
| Lot numbers | 8307694 |
| Model numbers | 309606 |
Product
3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2008-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.