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Consensus® Hip System
CONSENSUS ORTHOPEDICS, INC. · Model 1704-0-0048 · UDI-DI 00844588004124
JDL
Prescription
10
510(k) clearances
3,886
Adverse events (7 deaths)
5
Recalls
49
Facilities
Description
Acetabular Shell, No Hole, Cementless, PC
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-30 | Howmedica Osteonics Corp. | Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o |
| 2010-06-07 | Wright Medical Technology Inc | The inner and outer product packaging was missing the following information: shelf life, translations, manufacturing date, CE marking and also listed the incorrect sterilization m |
| 2009-05-14 | Wright Medical Technology Inc | Incorrect packaging, swapped sizes |
| 2009-05-14 | Wright Medical Technology Inc | Incorrect packaging, swapped sizes |
| 2004-01-09 | Stryker Howmedica Osteonics | This device is not approved for sale in the US. |
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Get your free API keyRead the docsData 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.
