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TELEFLEX LLC recalls Pilling Wecksorb Cylindrical Sponges
Recalled January 4, 2023 · FDA recall Z-0772-2023 · TELEFLEX
Hazard
Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised. · FDA Class II
Units
1,000 units
Sold at
Domestic distribution to IL, MS, PA, TN.
Description
Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.
Product
Pilling Wecksorb Cylindrical Sponges
Manufacturer(s)
TELEFLEX LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →