FDA Device Intelligence
Home › DEPUY ORTHOPAEDICS, INC. › RECLAIM

RECLAIM

DEPUY ORTHOPAEDICS, INC. · Model 10-185-4022 · UDI-DI 10603295533740

LZO Prescription
10
510(k) clearances
32,864
Adverse events (54 deaths)
177
Recalls
275
Facilities

Description

RECLAIM MONOBLOC REVISION FEMORAL STEM STANDARD STEM STANDARD OFFSET SO 22 CEMENTLESS

Recalls

DateFirmReason
2025-09-09BioPro, Inc.Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is impla
2025-03-24Zimmer, Inc.The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome femoral stems or stai
2025-03-24Zimmer, Inc.The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome femoral stems or stai
2025-03-24Zimmer, Inc.The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome femoral stems or stai
2025-03-24Zimmer, Inc.The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome femoral stems or stai
2025-03-24Zimmer, Inc.The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome femoral stems or stai
2025-02-12Zimmer, Inc.There is a potential design issue with the Z1 Offset Stem Inserter leading to fracturing of the distal tip.
2024-12-05Waldemar Link GmbH & Co. KG (Mfg Site)Error on the main label and the patient label. The labels indicate a size XXL, this is a standard-size neck segment.. All further information on the labels is correct (Length, CCD
2024-08-08Zimmer GmbHMislabeled: Incorrect sleeve in the packaging. The outer packaging is labeled as a standard neck sleeve, however, the product within the box is a -6mm neck sleeve, and vice versa.
2024-08-08Zimmer GmbHMislabeled: Incorrect sleeve in the packaging. The outer packaging is labeled as a standard neck sleeve, however, the product within the box is a -6mm neck sleeve, and vice versa.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.