Reported Apr 4, 2018 · Terminated
Persona Partial Knee Spacer Blocks To assist in partial knee arthroplasty surgery
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?
- Persona Partial Knee Spacer Blocks To assist in partial knee arthroplasty surgery
- Lot codes and dates
42-5399-035-08/09/10/12/14 (Sizes 8mm9mm10mm12mm14mm)
- Lot numbers
6355264463579568635472766357956963610265635490846357967463594433636102666354909663579676635944346361026763549097635796806359654763613101
- Amount recalled
- 430
This recall covers 20 products
The agency filed one notice per product. You are reading one of them; the other 19 are below.
7 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Zimmer Biomet is conducting a medical device recall for the Persona Partial Knee Spacer Blocks in sizes 8mm, 9mm, 10mm, 12mm, and 14mm. Complaints received indicated that flexion has the potential to feel tight during range-of-motion trialing and that the final trial has the potential to appear looser in extension.
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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