Reported Aug 3, 2022 · Ongoing
HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)
Paragon 28, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Paragon 28, Inc. · 14445 Grasslands Dr · Englewood, CO · 80112-7062
Is this the product you have?
HammerTube Implant2.75mm10¿ Cannulated (Sterile)
- Lot codes and dates
- Part NumberP40-002-0275-S
- UDI-DI Code(01)00889795033987(17)270323(10)26010822202
- Lot Number26010822202
- Amount recalled
- 9 implants
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Due to Titanium plasma coating not present implant.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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