VER2 DBL OFFSET RASP HANDLE, LT Nonsterile
Reported: August 20, 2014 Initiated: July 23, 2014 #Z-2224-2014
Product Description
VER2 DBL OFFSET RASP HANDLE, LT Nonsterile
Reason for Recall
The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
Details
- Recalling Firm
- Zimmer, Inc.
- Units Affected
- 412 units
- Distribution
- Worldwide Distribution-USA (nationwide) including the states of AK, AL, AZ, CA, CO, FL, GA, IN, KS, KY, MI, MN, NC, NJ, NY, OH, OK, OR, PA, SD, TN, TX, UT, and VA, and the countries of Australia, France, Germany, Italy, Switzerland, and Canada.
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
VER2 DBL OFFSET RASP HANDLE, LT Nonsterile. Recalled by Zimmer, Inc.. Units affected: 412 units.
Why was this product recalled? ▼
The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 20, 2014. Severity: Moderate. Recall number: Z-2224-2014.
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