Skip to content
RecallWatchMedical Device Safety
Manufacturer

Depuy (Ireland) recalls

The FDA has posted 11 enforcement recalls from Depuy (Ireland) since 2025, none of them Class I (most serious). Most recent report: Jul 8, 2026.

Class II: 11
Class IIOngoingZ-2617-2026

DEPUY (IRELAND) recalls Depuy Synthes

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

  • Metal/Polymer Cemented Constrained Femorotibial Knee Prosthesis
  • Under Investigation by firm
DEPUY (IRELAND)Jul 8, 2026
Class IIOngoingZ-2616-2026

DEPUY (IRELAND) recalls Depuy Synthes

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

  • Metal/Polymer Cemented Constrained Femorotibial Knee Prosthesis
  • Under Investigation by firm
DEPUY (IRELAND)Jul 8, 2026
Class IIOngoingZ-1988-2026

DEPUY (IRELAND) recalls Depuy Synthes

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

  • Metal/Polymer Cemented Constrained Femorotibial Knee Prosthesis
  • Under Investigation by firm
DEPUY (IRELAND)May 6, 2026
Class IIOngoingZ-1986-2026

DEPUY (IRELAND) recalls Depuy Synthes

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

  • Metal/Polymer Cemented Constrained Femorotibial Knee Prosthesis
  • Under Investigation by firm
DEPUY (IRELAND)May 6, 2026
Class IIOngoingZ-1991-2026

DEPUY (IRELAND) recalls Depuy Synthes

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

  • Metal/Polymer Cemented Constrained Femorotibial Knee Prosthesis
  • Under Investigation by firm
DEPUY (IRELAND)May 6, 2026
Class IIOngoingZ-1993-2026

DEPUY (IRELAND) recalls Depuy Synthes

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

  • Metal/Polymer Cemented Constrained Femorotibial Knee Prosthesis
  • Under Investigation by firm
DEPUY (IRELAND)May 6, 2026
Class IIOngoingZ-1987-2026

DEPUY (IRELAND) recalls Depuy Synthes

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

  • Metal/Polymer Cemented Constrained Femorotibial Knee Prosthesis
  • Under Investigation by firm
DEPUY (IRELAND)May 6, 2026
Class IIOngoingZ-1989-2026

DEPUY (IRELAND) recalls Depuy Synthes

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

  • Metal/Polymer Cemented Constrained Femorotibial Knee Prosthesis
  • Under Investigation by firm
DEPUY (IRELAND)May 6, 2026
Class IIOngoingZ-1992-2026

DEPUY (IRELAND) recalls Depuy Synthes

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

  • Metal/Polymer Cemented Constrained Femorotibial Knee Prosthesis
  • Under Investigation by firm
DEPUY (IRELAND)May 6, 2026
Class IIOngoingZ-1985-2026

DEPUY (IRELAND) recalls Depuy Synthes

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

  • Metal/Polymer Cemented Constrained Femorotibial Knee Prosthesis
  • Under Investigation by firm
DEPUY (IRELAND)May 6, 2026
Class IIOngoingZ-1990-2026

DEPUY (IRELAND) recalls Depuy Synthes

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

  • Metal/Polymer Cemented Constrained Femorotibial Knee Prosthesis
  • Under Investigation by firm
DEPUY (IRELAND)May 6, 2026

Firm name as filed with the FDA: “DEPUY (IRELAND)”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.