Reported Sep 25, 2013 · Terminated
OSTEORAPTOR 2.3 mm with 1 ULTRABRAID Suture, White; Part Number: 72201991 Biodegradable suture anchor
Smith & Nephew, Inc. Endoscopy Division
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. Endoscopy Division · 150 Minuteman Drive · Andover, MA · 01810-1031
Is this the product you have?
- OSTEORAPTOR 2.3 mm with 1 ULTRABRAID Suture, White
- Part Number72201991 Biodegradable suture anchor
- Lot codes and dates
193 of 193 codes
502723335027246050272749502730925027414550274574502771045027753150278113502816605028302250283200502838505028545050287132502900445029033650292248502937205029581750298408503016895030207750305597503076165030761750307618503076635030892450308925503089265030940650309508503107795031175550312497503147315031617850316439503177605031897050320251503206725032164350321930503229295032401750325608503266985032782050329812503316905033290550334815503365295033942650340626503416185034300450343606
- Amount recalled
- 22879 US
This recall covers 26 products
The agency filed one notice per product. You are reading one of them; the other 25 are below.
13 more are in the archive.
Where it was sold
- Nationwide
- PR
Why it was recalled
Pinholes detected in a small number of primary pouches that may constitute a breach of the sterile barrier.
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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