ClearanceBrief
Recall Z-1269-2020 ยท DWS Instruments, Surgical, Cardiovascular

TELEFLEX MEDICAL INC

Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440

DateJan 27, 2020 (initiated Jan 13, 2020)
StatusTerminated
ReasonThere is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.
Root causeUnder Investigation by firm
ActionThe 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
Quantity1764 units
DistributionWorldwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.