Recall archive / FDA device enforcement
Pilling Wecksorb Cylindrical Sponges — FDA record Z-0772-2023
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Sep 28, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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.
- Classification
- Class II
- Recalling firm
- TELEFLEX LLC
- Quantity
- 1,000 units
- Agency-reported status
- Terminated
- Source record identifier
- Z-0772-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Catalog Number: 200400, Lot Number: 22B0395 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Domestic distribution to IL, MS, PA, TN.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jan 4, 2023
- Recall initiation date
- Sep 28, 2022
- Center classification date
- Dec 28, 2022
- Termination date
- Jul 24, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.