---
title: "Pilling Wecksorb Cylindrical Sponges — FDA record Z-0772-2023 | Is It on Recall"
description: "Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised."
url: https://isitonrecall.com/recall/fda-device-z-0772-2023-pilling-wecksorb-cylindrical-sponges/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / 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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## 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

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0772-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). 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.

- [Illinois](https://isitonrecall.com/state/illinois/)
- [Mississippi](https://isitonrecall.com/state/mississippi/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)

## 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.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0772-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [TELEFLEX LLC records](https://isitonrecall.com/brand/teleflex-llc/)