EasyPoint Needle — Class II medical device recall Z-1293-2024
Ongoing recall by Retractable Technologies, Inc., reported 2024-03-20, distributed nationwide. The needle cannula of a retractable needle may detach from the needle holder in the patient.
| Recall number | Z-1293-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Retractable Technologies, Inc., Little Elm, TX, United States |
| Recall initiated | 2024-02-05 |
| Classified | 2024-03-14 |
| Reported by FDA | 2024-03-20 |
| Distributed | Nationwide (US) |
| Quantity | 477,600 |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00613703820907 |
| Lot numbers | K220402 |
| Model numbers | 82091 |
| Expiration dates | 2027-03-28 |
Product
EasyPoint Needle, 25G x 5/8", REF: 82091
Reason for recall
The needle cannula of a retractable needle may detach from the needle holder in the patient.
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-1293-2024. 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.