Reported Dec 6, 2017 · Terminated
ROSA Surgical Device 2.5.8
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. · 1800 W Center St · Warsaw, IN · 46580-2304
Is this the product you have?
- ROSA Surgical Device 2.5.8
- Lot codes and dates
Serial No. RO10011RO10014RO13023 and RO13027
- Amount recalled
- 22 units (4 US and 18 OUS)
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Issue with optional neuro-endoscopy module detected under specific conditions during internal testing.
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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