TELEFLEX MEDICAL INC Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440
Brand
TELEFLEX MEDICAL INC
Lot Codes / Batch Numbers
Lot Number 74B1500674
Products Sold
Lot Number 74B1500674
TELEFLEX MEDICAL INC is recalling Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440 due to There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.
Recommended Action
Per FDA guidance
The firm initiated the recall by letter on 01/13/2020. The actions to be taking be the consignees are as follows: Check inventory. If affected stock is found, discontinue use immediately and quarantine. Complete the acknowledgement form as soon as possible indicating whether you do or do not have stock and fax it 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. For additional questions, contact the local sales representative or Customer Service at 1-866-396-2111.
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 noticePage updated: Jan 10, 2026