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Paragon 28, Inc. recalls HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)
Recalled August 3, 2022 · FDA recall Z-1468-2022 · Paragon 28
Hazard
Due to Titanium plasma coating not present implant. · FDA Class II
Units
9 implants
Sold at
U.S. Nationwide distribution in the states of AL, CA, GA, IL and KY.
Description
Due to Titanium plasma coating not present implant.
Product
HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)
Manufacturer(s)
Paragon 28, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →