TELEFLEX LLC Pilling Wecksorb Cylindrical Sponges Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pilling Wecksorb Cylindrical Sponges
Brand
TELEFLEX LLC
Lot Codes / Batch Numbers
Catalog Number: 200400, Lot Number: 22B0395
Products Sold
Catalog Number: 200400, Lot Number: 22B0395
TELEFLEX LLC is recalling Pilling Wecksorb Cylindrical Sponges due to Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IL, MS, PA, TN
Page updated: Jan 10, 2026