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Integra LifeSciences Corp. recalls Panta Nail, Rx only, Sterile,
Recalled March 29, 2017 · FDA recall Z-1539-2017 · Integra LifeSciences
Hazard
Voluntary recall/Removal of Panta and Panta XI Nails because there may be the potential that the internal and external package seal does not provide the level of sterility intended. · FDA Class II
Units
4,449 units
Sold at
US Nationwide and Internationally
Description
Voluntary recall/Removal of Panta and Panta XI Nails because there may be the potential that the internal and external package seal does not provide the level of sterility intended.
Product
Panta Nail, Rx only, Sterile,
Manufacturer(s)
Integra LifeSciences Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →