Pilling Wecksorb Cylindrical Sponges — Class II medical device recall Z-0772-2023
Terminated recall by TELEFLEX LLC, reported 2023-01-04, distributed in IL, MS, PA, TN. Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected produ
| Recall number | Z-0772-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | TELEFLEX LLC, Morrisville, NC, United States |
| Recall initiated | 2022-09-28 |
| Classified | 2022-12-28 |
| Reported by FDA | 2023-01-04 |
| Terminated | 2026-07-24 |
| Distributed | IL, MS, PA, TN |
| Quantity | 1,000 units |
| Reason classes | sterility |
| Lot numbers | 22B0395 |
| Model numbers | 200400 |
Product
Pilling Wecksorb Cylindrical Sponges
Reason for recall
Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.
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-0772-2023. 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.