Warning
DEPUY (IRELAND) Recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #Z-1992-2026Medical Device
DEPUY (IRELAND) Recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM
DEPUY (IRELAND) · Class II — Moderate Risk
Product Description
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.
Reason for Recall
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
US Nationwide distribution in the states of MN, NC, TX.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
DEPUY (IRELAND) has recalled a medical device that the FDA classified as Class II affecting 3 units. The recall was initiated on April 3, 2026. The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. It was distributed in MN, NC, TX. Class II recalls involve products that might cause a temporary health problem or pose only a slight threat of a serious nature. Consumers should discontinue use and contact the firm.
Sources: FDA openFDA Enforcement Database
This recall appears in: Medical Device Defects.