Alloclassic SL Shaft — Class II medical device recall Z-0210-2013
Terminated recall by Zimmer, Inc., reported 2012-11-14, distributed nationwide. Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 2010 by th
| Recall number | Z-0210-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2012-09-04 |
| Classified | 2012-11-06 |
| Reported by FDA | 2012-11-14 |
| Terminated | 2014-04-16 |
| Distributed | Nationwide (US) |
| Quantity | 1,355 |
| Reason classes | labeling |
| Lot numbers | 2301633, 2303201, 2303302, 2316056, 2319316, 2326792, 2333704, 2335608, 2335862, 2340681, 2340906, 2343382, 2345324, 2345382, 2347856, 2352268, 2355428, 2355765, 2355767, 2359179, 2359249, 2359251, 2361511, 2363829, 2368739, 2368928, 2370478, 2370490, 2371517, 2375002, 2376476, 2376478, 2381324, 2382854, 2387449, 2388530, 2388539, 2388541, 2390171, 2391015 and 58 more |
| Model numbers | 2301633, 2303201, 2303302, 2316056, 2319316, 2326792, 2333704, 2335608, 2335862, 2340681, 2340906, 2343382, 2345324, 2345382, 2347856, 2352268, 2355428, 2355765, 2355767, 2359179, 2359249, 2359251, 2361511, 2363829, 2368739 and 91 more |
Product
Alloclassic SL Shaft
Reason for recall
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
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.