Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Teleflex Pilling Aortic Punch Recalled by Deroyal Industries, Inc. Lafollette Due to The sterile packaging has the potential to be...
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 Deroyal Industries, Inc. Lafollette directly.
Affected Products
Teleflex Pilling Aortic Punch, 4.0mm. Sterile, Rx Only, disposable. Included as part of Intl-Cardiac Surgery Kit - Product Usage: This device is used for cardiovascular surgical procedures.
Quantity: 669 units
Why Was This Recalled?
The sterile packaging has the potential to be compromised.
Where Was This Sold?
International distribution of Kuwait City, Kuwait.
About Deroyal Industries, Inc. Lafollette
Deroyal Industries, Inc. Lafollette has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report