Reported Nov 14, 2012 · Terminated
Alloclassic SL Shaft
Zimmer, Inc.
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: Zimmer, Inc. · 345 E Main St · Warsaw, IN · 46580-2746
Is this the product you have?
- Alloclassic SL Shaft
- Lot codes and dates
Item 28392840284128422843284428452846284728482949285128522883288428852886
- and 2887 Lots
120 of 120 codes
235924923592512359251236873924139142413914242601025261382335608238132423874492388541240123724012372492774252355323557672355767236151123615112371517237647624406722453100247973624983632529208230330223478562355765235576524282472428247244669924563532497037250606725060672509374251749423160562326792233586223554282370478237647823828542388539239120424287422431991243973324530932301633234338223638292363829236382923704902492887
- Amount recalled
- 1355
This recall covers 40 products
The agency filed one notice per product. You are reading one of them; the other 39 are below.
27 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 2010 by the Zimmer GmbH production site in Winterthur, 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
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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