RecallDepth

Pilling Wecksorb Cylindrical Sponges

This recall is currently active, issued December 28, 2022. It was issued by Teleflex Llc.

Company
Teleflex Llc
Recall Initiated
September 28, 2022
Posted
December 28, 2022
Recall Number
Z-0772-2023
Quantity
1,000 units
Firm Location
Morrisville, NC
Official Source
View on FDA website ↗

Reason for Recall

Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.

Distribution

Domestic distribution to IL, MS, PA, TN.

Lot / Code Info

Catalog Number: 200400, Lot Number: 22B0395

Root Cause

Nonconforming Material/Component

Action Taken

Consignees were notified on about 09/28/2022, via letter. Consignees were instructed to immediately discontinue use and quarantine the products on hand, complete and return the enclosed Acknowledgement Form via fax to 1-855-419-8507 or email to recalls@teleflex.com. A customer service representative will contact you with a Return Goods Authorization (RGA) number and provide instructions for the return of products.

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