Reported Nov 29, 2017 · Terminated
ROSA Surgical Device 2.5.8 It is intended to be used in the operating room for the spatial positioning and orientation…
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 It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed with three-dimensional imaging software, and uses fiducial markers or optical registration. The system is intended for use by neurosurgeons to guide standard neurosurgical instruments. It is indicated for any neurosurgical condition in which the use of stereotactic surgery may be appropriate.
- Lot codes and dates
Serial No. RO10011RO14033RO14031RO14035RO13027RO13023RO10014RO10009RO10010RO14030RO11016RO11017RO12022RO14029RO14032RO08003RO09004RO10007RO10013RO12018RO12019RO13025RO14034RO11015RO13024RO09005RO13026RO12021and RO12020
- Amount recalled
- 29 devices(8 US and 21 OUS)
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
Why it was recalled
Software corrections reactivating the cooperative endoscopy mode.
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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