Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Teleflex Medical Disposable Aortic Punch Recalled by TELEFLEX MEDICAL INC Due to There is a potential for the device packaging...
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
Teleflex Medical Disposable Aortic Punch, in the following sizes: a) 2.8 mm, REF DP-28K b) 3.6 mm, REF DP-36K c) 4.0 mm, REF DP-40K d) 4.4 mm, REF DP-44K e) 4.8 mm, REF DP-48K f) 5.2 mm, REF DP-52K g) 5.6 mm, REF DP-56K h) 6.0 mm, REF DP-60K i) 2.8 mm, REF MDP-28K j) 3.6 mm, REF MDP-36K k) 4.0 mm, REF MDP-40K l) 4.4 mm, REF MDP-44K m) 4.8 mm, REF MDP-48K n) 5.2 mm, REF MDP-52K o) 5.6 mm, REF MDP-56K p) 6.0 mm, REF MDP-60K
Quantity: 587066 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.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report