RECLAIM DISTAL TAPERED Distal Stem — Class II medical device recall Z-2084-2014
Terminated recall by DePuy Orthopaedics, Inc., reported 2014-07-30, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. The product can be difficult to remove from the Distal Stem both out of the package and after proximal reaming
| Recall number | Z-2084-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Orthopaedics, Inc., Warsaw, IN, United States |
| Recall initiated | 2014-06-03 |
| Classified | 2014-07-20 |
| Reported by FDA | 2014-07-30 |
| Terminated | 2017-05-17 |
| Distributed | AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV |
| Countries outside the US | AT, AU, CA, CH, CL, CN, CZ, DE, DK, ES, FR, GB, IE, IL, IT, NO, NZ, PL, SG, SI, ZA |
| Quantity | 3,623 |
| Lot numbers | 107310, 107311, 107313, 107314, 107315, 107320, 107323, 107325, 107328, 107330, 107331, 107333, 107334, 107336, 107338, 107339, 107340, 136244, 136247, 136251, 136252, 136256, 136257, 136262, 136268, 136271, 136276, 136286, 136369, 136370, 136371, 136372, 136373, 136374, 136375, 136376, 136377, 136377A, 136378, 136380 and 460 more |
Product
RECLAIM DISTAL TAPERED Distal Stem, various sizes. Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the locking taper surface of the Distal Stem is protected during proximal preparation.
Reason for recall
The product can be difficult to remove from the Distal Stem both out of the package and after proximal reaming.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2084-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
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.