Fresh Recalls

FDAClass II · Medical device · Recall Z-2461-2026 · Recalled June 24, 2026

TRI TS BASEPLATE SIZE 3 recall — Howmedica Osteonics Corp.

Agency report date: June 24, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
TRI TS BASEPLATE SIZE 3
Company / brand
Howmedica Osteonics
Lot / serial / date codes
Part Number: 5521-B-300. UDI: (01)07613327026313(17)260921(10) UZD9IB. Lot Number: UZD9IB.
Distribution
US Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.
Agency product description and boundaries

TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: TRI TS BASEPLATE SIZE 3 recall status

3. Open the official notice or contact

Official recall ID
Z-2461-2026
Brand
All Howmedica Osteonics recalls
Classification
Class II
Units affected
7 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Mahwah, NJ, United States
Firm address
325 Corporate Dr, 07430-2006

Identifying details (verbatim from the notice)

Product codes / lots
Part Number: 5521-B-300. UDI: (01)07613327026313(17)260921(10) UZD9IB. Lot Number: UZD9IB.
Distribution
US Nationwide distribution in the states of AZ, CA, GA, MI, NC, NJ, NY, WV.
Firm notified the public via
Letter
FDA event ID
99080
Recall initiated
May 19, 2026
FDA classified
June 17, 2026
FDA report date
June 24, 2026

Other medical device recalls from around the same time

Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved September 22, 2026 at 6:00 PM UTC.

Report a data error on this page