HIGH

Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.

The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

Quick Facts at a Glance

Recall Date
April 3, 2026
Hazard Level
HIGH
Brand
DEPUY
Geographic Scope
1 states

Hazard Information

The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact DEPUY (IRELAND) or your healthcare provider for instructions. Notification method: E-Mail

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Full Description

Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.. Reason: The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.. Classification: Class II. Quantity: 3 units. Distribution: US Nationwide distribution in the states of MN, NC, TX.

View Original Recall on FDA - Medical Devices

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Product Classification

Product Details

Brand
DEPUY
Model Numbers
Part Number: 150450107. UDI-DI: 10603295533139. Lot Number: 1006440. Expiration Date: 11/30/2035.
Affected States
ALL
Report Date
May 6, 2026
Recall Status
ACTIVE

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