Reported Nov 29, 2023 · Ongoing
Compress Device Segmental Anchor Plug, 10 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or…
Biomet, 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: Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
- Compress Device Segmental Anchor Plug, 10 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement
- Item Number178400
- Lot codes and dates
- Lot Numbers/UDI 541470 (01)00880304259690(17)270629(10)541470 608490 (01)00880304259690(17)280302(10)608490 608580 (01)00880304259690(17)271030(10)608580 609140 (01)00880304259690(17)271112(10)609140 671410 (01)00880304259690(17)271030(10)671410 671650 (01)00880304259690(17)271030(10)671650 856920 (01)00880304259690(17)271030(10)856920
- Amount recalled
- N/A
This recall covers 19 products
The agency filed one notice per product. You are reading one of them; the other 18 are below.
6 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery
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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