Cartilage Knee Brace***LATEX FREE" Product Usage: Used in the treatment and support of many types of knee injuries or following surgical and nonsurgical correction.
Reported: May 21, 2014 Initiated: March 19, 2014 #Z-1604-2014
Product Description
Cartilage Knee Brace***LATEX FREE" Product Usage: Used in the treatment and support of many types of knee injuries or following surgical and nonsurgical correction.
Reason for Recall
During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex.
Details
- Recalling Firm
- Zimmer, Inc.
- Units Affected
- 2,222 units
- Distribution
- Worldwide Distribution - US Nationwide in the states of: AK, AZ, CA, FL, GA, IA, IL, IN, LA, MD, MI, MO NC, NE, NV, NY, OH, OK, OR, PA, RI, SD, TX, UT, VA, VT, WA, WI & WV and countries of: AUSTRALIA, CANADA, GERMANY, IRAQ, ITALY, SAUDI ARABIA, TUNISIA & UNITES ARAB EMIRATES.
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
Cartilage Knee Brace***LATEX FREE" Product Usage: Used in the treatment and support of many types of knee injuries or following surgical and nonsurgical correction.. Recalled by Zimmer, Inc.. Units affected: 2,222 units.
Why was this product recalled? ▼
During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 21, 2014. Severity: Moderate. Recall number: Z-1604-2014.
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