ClearanceBrief
Recall Z-1992-2026 · KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

DEPUY (IRELAND)

Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.

DateApr 29, 2026 (initiated Apr 3, 2026)
StatusOpen, Classified
ReasonThe external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Root causeUnder Investigation by firm
ActionDepuy Ireland notified consignees on about 04/03/2026 via email. Consignees were instructed to examine inventory for affected units and immediately quarantine them, arrange for the return of all affected units, and complete and return the provided Business Response Form. Consignees were also instructed to forward the notification letter to anyone within each facility that needs to be informed, notify customers if affected units were further distributed and post a copy of the notification letter in a visible area for awareness.
Quantity3 units
DistributionUS Nationwide distribution in the states of MN, NC, TX.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K242871ATTUNE™ Revision Hinge Knee
Depuy Ireland UC, Nov 21, 2024