FDA-Device2022-08-03Class II
HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)
Paragon 28, Inc.
Hazard
Due to Titanium plasma coating not present implant.
Sold states
U.S. Nationwide distribution in the states of AL, CA, GA, IL and KY.
Affected count
9 implants
Manufactured in
14445 Grasslands Dr, Englewood, CO, United States
Products
HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1468-2022Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief