Recall Z-1604-2014— Zimmer, Inc.
Class II · Terminated
Class II FDA medical device recall by Zimmer, Inc., initiated 2014-03-19, terminated 2015-04-14. FDA's recall record names no specific 510(k) clearance for this event. Product: 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: During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex..
- Recalling firm
- Zimmer, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-03-19
- Terminated
- 2015-04-14
- Firm location
- Warsaw, IN, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.