FDA Device recall Z-0772-2023
Pilling Wecksorb Cylindrical Sponges
- FDA Device
- Class II
- terminated
- Published 2023-01-04
On 2023-01-04 the FDA classified a Class II recall of Pilling Wecksorb Cylindrical Sponges by Teleflex, citing specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0772-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-09-28 |
| Published | 2023-01-04 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Teleflex |
| Distribution | IL, MS, PA, TN |
Product
Pilling Wecksorb Cylindrical Sponges
Reason
Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.
Identifiers
| code_info | Catalog Number: 200400, Lot Number: 22B0395 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0772-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.