FDA Recall Database: Class II Recall: Comprehensive Shoulder Stem, Comprehensive Micro Stem, Comprehensive Mini… by ZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAY

Key facts

What consumers should do

Facilities, clinicians, and consumers holding an affected unit or lot of Comprehensive Shoulder Stem, Comprehensive Micro Stem, Comprehensive Mini Stem; uncemented shoulder prosthesis, Model Nos. 113605, 113606, 113607, 113627 should stop using it for the purpose described in the recall notice and hold remaining stock pending instructions from ZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAY. 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 ORTHOPEDICS MANFACTURING LIMITED-GALWAY 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 ORTHOPEDICS MANFACTURING LIMITED-GALWAY 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 ORTHOPEDICS MANFACTURING LIMITED-GALWAY’s FDA history

Argus HQ has recorded 1 total FDA action tied to ZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAY: 0 warning letters, 1 recall, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

Why was Comprehensive Shoulder Stem, Comprehensive Micro Stem, Compr recalled?

FDA's recall record states the reason as: Five complaints received where surgeon was unable to remove and/or connect the inserter with the stem during surgery due to excess material remaining within the taper. Issue may lead to clinically significant extension of surgery to find a replacement.

Who should I contact about this recall?

Contact ZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAY 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 ORTHOPEDICS MANFACTURING LIMITED-GALWAY had other FDA recalls or enforcement actions?

This is the only FDA action Argus HQ has on file for ZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAY so far. Argus ingests new FDA enforcement records daily.

What is the FDA recall number for this event?

FDA recall number Z-1403-2025.

Related enforcement actions