Reported Feb 17, 2016 · Terminated
Reuseable rotary blade/abrader, product number 899751504. The oval burr laterally hooded is an attachment or accessory…
Richard Wolf Medical Instruments Corp.
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: Richard Wolf Medical Instruments Corp. · 353 Corporate Woods Pkwy · Vernon Hills, IL · 60061-3110
Is this the product you have?
- Reuseable rotary blade/abrader, product number 899751504. The oval burr laterally hooded is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
- Lot codes and dates
- Affected lot 0207201502.
- Amount recalled
- four units
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
Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proximal end making the product dysfunctional.
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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