FDA Recall Database: Class II Recall: Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type… by Zimmer, Inc.

Key facts

What consumers should do

Facilities, clinicians, and consumers holding an affected unit or lot of 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 should stop using it for the purpose described in the recall notice and hold remaining stock pending instructions from Zimmer, Inc.. FDA recall records typically direct the recalling firm to notify known accounts directly with a recall letter describing the specific corrective action -- replacement, field correction, refund, or return. Anyone who received the product through a distributor rather than directly from Zimmer, Inc. should confirm with their supplier whether their specific lot or unit is on the affected list, since recall notices are lot- or unit-specific and not every unit of a product line is necessarily included. Questions about a specific unit's status should go to Zimmer, Inc. directly or to the distributor that supplied it; Argus HQ is a public-record aggregator, not the recalling firm, and cannot confirm individual unit status.

What this classification means

A Class II recall is FDA’s middle classification. FDA assigns Class II when use of, or exposure to, the recalled product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote. FDA still requires the recalling firm to notify affected accounts and submit status reports on the correction, though the monitoring intensity is lower than for a Class I recall. FDA's Center for Devices and Radiological Health (for devices) or Center for Drug Evaluation and Research (for drugs) reviews the classification and can require additional corrective action if the initial response is judged insufficient. Because this record is filed as Class II, professionals and consumers handling an affected lot should treat FDA's own classification -- not this page's summary of it -- as the authoritative risk signal. A Class I recall is FDA’s most serious classification. FDA assigns Class I when there is a reasonable probability that use of, or exposure to, the recalled product will cause serious adverse health consequences or death. This classification does not mean harm has already occurred in every case -- it reflects FDA’s assessment of the realistic worst-case risk profile of the defect described in the recall, based on the reason for recall reported by the firm. Class I recalls receive the closest FDA monitoring of the three classes: the recalling firm typically must submit a recall strategy, periodic status reports, and effectiveness checks confirming that the affected lots have actually been removed from distribution or corrected in the field.

Zimmer, Inc.’s FDA history

Argus HQ has recorded 66 total FDA actions tied to Zimmer, Inc.: 0 warning letters, 66 recalls, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

Why was Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +3 Nec recalled?

FDA's recall record states the reason as: 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.

Who should I contact about this recall?

Contact Zimmer, Inc. directly, or the distributor/pharmacy that supplied the product, to confirm whether your specific lot or unit is affected. Argus HQ aggregates the public FDA recall record and is not the recalling firm.

Has Zimmer, Inc. had other FDA recalls or enforcement actions?

Yes. Argus HQ has recorded 66 total FDA actions tied to Zimmer, Inc., including 66 recalls and 0 warning letters.

What is the FDA recall number for this event?

FDA recall number Z-1649-2025.

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