Class II — TELEFLEX LLC
| Recalling firm | Teleflex |
|---|---|
| Registered facility | View this company's 9 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised. |
| Product | Pilling Wecksorb Cylindrical Sponges |
| Quantity | 1,000 units |
| Distribution | Domestic distribution to IL, MS, PA, TN. |
| Initiated | 2022-09-28 |
| Classified | 2022-12-28 |
| Terminated | 2026-07-24 |
| Recall number | Z-0772-2023 |
| 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 — TELEFLEX LLC (Z-0772-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91312/
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