Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Pilling Aortic Punch Recalled by TELEFLEX MEDICAL INC Due to There is a potential for the device packaging...

Date: January 13, 2020
Company: TELEFLEX MEDICAL INC
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact TELEFLEX MEDICAL INC directly.

Affected Products

Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440

Quantity: 1764 units

Why Was This Recalled?

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

Where Was This Sold?

Worldwide

About TELEFLEX MEDICAL INC

TELEFLEX MEDICAL INC has 32 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report