Reported Oct 28, 2020 · Ongoing
TWINFIX ULTRA HA 4.5 W/2 UB BLUE & BLK- Absorbable Suture anchor Product Number: 72202624
Smith & Nephew, 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: Smith & Nephew, Inc. · 150 Minuteman Rd · Andover, MA · 01810-1031
Is this the product you have?
- TWINFIX ULTRA HA 4.5 W/2 UB BLUE & BLK-
- Absorbable Suture anchor Product Number72202624
- Lot codes and dates
- Batch Numbers2013904 2018628 2023177 2025213 2039590 2050959 2052719
- Amount recalled
- 263,874 (total)
This recall covers 41 products
The agency filed one notice per product. You are reading one of them; the other 40 are below.
28 more are in the archive.
Where it was sold
Why it was recalled
Product packaging improper or incomplete seal of the pouch surrounding the sterile product may result in a breach of the sterile barrier created by the pouch
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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