The Recall Desk

FDA (Devices) recall action 96493

Zimmer, Inc. recalled 5 products on 2025-04-30

The FDA (Devices) publishes a recall like this one as 5 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 5 pages.

Products
5
Announced
2025-04-30
Critical
0
Units
1,116

Why these products were recalled

The associated product labeling does not adequately provide compatibility information for use of the 22.2 mm Diameter Ceramic Femoral Heads with cobalt-chrome femoral stems or stainless-steel femoral stems.

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

1–5 of 5

  • ModerateFDA (Devices)··2025-04-30

    Zimmer Biomet Ceramic Hip Prosthesis Head Lacks Stem Compatibility Information

    Zimmer, Inc. is recalling a ceramic hip prosthesis head because its labeling does not adequately describe compatibility with cobalt-chrome or stainless-steel femoral stems.

    Product
    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +0 Neck, Model Number 802602202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
    Category
    Distribution
    0 states
  • ModerateFDA (Devices)··2025-04-30

    Zimmer Biomet Ceramic Hip Prosthesis Heads Lack Stem Compatibility Information

    Zimmer, Inc. is recalling Zimmer Biomet Ceramic Head hip prostheses (Model 802802201, 22.2 mm diameter) because product labeling does not adequately provide compatibility information for use with cobalt-chrome or stainless-steel femoral stems.

    Product
    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, -3 Neck, Model Number 802802201; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
    Category
    Distribution
    0 states
  • ModerateFDA (Devices)··2025-04-30

    Zimmer Biomet Ceramic Femoral Head Hip Prosthesis Labeling Recall

    Zimmer, Inc. is recalling a ceramic femoral head hip prosthesis (Model 802602203) because product labeling lacks compatibility information for use with cobalt-chrome or stainless-steel femoral stems.

    Product
    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +3 Neck, Model Number 802602203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
    Category
    Distribution
    0 states
  • ModerateFDA (Devices)··2025-04-30

    Zimmer Biomet Ceramic Hip Head 22.2 mm Lacks Stem Compatibility Information

    Zimmer, Inc. is recalling a ceramic hip prosthesis head because the product labeling does not adequately describe compatibility with certain femoral stems used in hip replacement surgery.

    Product
    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +3 Neck, Model Number 802802203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
    Category
    Distribution
    0 states
  • ModerateFDA (Devices)··2025-04-30

    Zimmer Biomet Ceramic Hip Prosthesis Head Lacks Compatibility Labeling

    Zimmer, Inc. is recalling a ceramic femoral head for hip prosthesis (Model 802802202, 22.2 mm) because product labeling does not adequately describe compatibility with certain metal femoral stems.

    Product
    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +0 Neck, Model Number 802802202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
    Category
    Distribution
    0 states