Fitmore" Hip Stem
Reported: November 14, 2012 Initiated: September 4, 2012 #Z-0220-2013
Product Description
Fitmore" Hip Stem
Reason for Recall
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
Details
- Recalling Firm
- Zimmer, Inc.
- Units Affected
- 1190
- Distribution
- Nationwide Distribution.
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
Fitmore" Hip Stem. Recalled by Zimmer, Inc.. Units affected: 1190.
Why was this product recalled? ▼
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Wintetthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 14, 2012. Severity: Moderate. Recall number: Z-0220-2013.
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