Class II — Retractable Technologies, Inc.
| Recalling firm | RETRACTABLE TECHNOLOGIES, INC. |
|---|---|
| Registered facility | RETRACTABLE TECHNOLOGIES, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The needle cannula of a retractable needle may detach from the needle holder in the patient. |
| Product | EasyPoint Needle, 25G x 5/8", REF: 82091 |
| Quantity | 477,600 |
| Distribution | US Nationwide distribution including in the states of NY, FL, IL, MA, UT, NJ, AZ, MO, WA, NC, CA, TX, NV, IN, PA, VA, IA, GA, TN, MI, OH, OK, CO, OR, SC, MN, CT. |
| Initiated | 2024-02-05 |
| Classified | 2024-03-14 |
| Recall number | Z-1293-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Retractable Technologies, Inc. (Z-1293-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93981/
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