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TELEFLEX MEDICAL INC recalls Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440
Recalled February 26, 2020 · FDA recall Z-1269-2020 · TELEFLEX MEDICAL
Hazard
There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed. · FDA Class II
Units
1764 units
Sold at
Worldwide
Description
There is a potential for the device packaging to become compromised; thus, the sterility of the device cannot be guaranteed.
Product
Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440
Manufacturer(s)
TELEFLEX MEDICAL INC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →