Reported Dec 12, 2018 · Terminated
Biomet 20mm Compress Device Short Anchor Plug With Drill Set / With Pin Inserter Ion Implant Item number: 178562…
Zimmer 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: Zimmer Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
4 of 4 products
| # | Product as published |
|---|---|
| 1 | Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. |
| 2 | Tumor resections. |
| 3 | Revision of previously failed total joint arthroplasty. |
| 4 | Trauma. The Compress¿ Segmental Femoral Replacement System (Short Spindle and Anchor Plug) components are intended for uncemented use only. |
- Lot codes and dates
- Lot Number608740
- UDI Number(01)00880304461666(17)271113(10)608740
- Amount recalled
- 6 units
This recall covers 14 products
The agency filed one notice per product. You are reading one of them; the other 13 are below.
1 more are in the archive.
Where it was sold
Why it was recalled
Potential metal burrs in the holes of the device preventing the appropriate drill and transverse pins from being inserted
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.
Free recall alerts
Get alerted about new Zimmer Biomet, Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.