BD Stimex Insulated Needle 22G x 2 — Class II medical device recall Z-0923-2021
Terminated recall by Becton Dickinson & Company, reported 2021-02-03, distributed in AL, CT, FL, IL, IN, MI, MO, MS…. BD was advised by the European Notified Body, NSAI, that the instructions for use (IFU) needs to be updated to
| Recall number | Z-0923-2021 |
|---|---|
| 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 | 2020-12-09 |
| Classified | 2021-01-26 |
| Reported by FDA | 2021-02-03 |
| Terminated | 2022-08-10 |
| Distributed | AL, CT, FL, IL, IN, MI, MO, MS, NC, NE, NV, NY, PA, RI, TN, TX, UT, VA |
| Countries outside the US | AU, BE, CA, SG |
| Quantity | 16,250 units |
| UPC / GTIN / UDI-DI | 50382904042047 |
| Model numbers | 404204 |
Product
BD Stimex Insulated Needle 22G x 2.13in ( 50 units/cs.) Indicated for administration of medications to affect anesthesia or analgesia to a specific anatomical location (region). Catalog No. 404204
Reason for recall
BD was advised by the European Notified Body, NSAI, that the instructions for use (IFU) needs to be updated to include the general contraindications
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-0923-2021. 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.