TELEFLEX MEDICAL INC: Medical Device Recall in 2020 - (Recall #: Z-1269-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440

Product Classification:

Class II

Date Initiated: January 13, 2020

Date Posted: February 26, 2020

Recall Number: Z-1269-2020

Event ID: 84722

Reason for Recall:

There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.

Status: Terminated

Product Quantity: 1764 units

Code Information:

Lot Number 74B1500674

Distribution Pattern:

Worldwide

Voluntary or Mandated:

Voluntary: Firm initiated