FDA DeviceClass IINotable

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

Date: 2026-06-24
Brand: Howmedica Osteonics Corp.
Category: Medical Device
FDA Class: Class II

Description

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).

Hazard

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).

Remedy

7 units

View original recall →
Share:

Related Recalls

2026-06-24 · FDA_DEVICE
FDA Recall: TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.
Howmedica Osteonics Corp.
2026-03-25 · FDA_DEVICE
FDA Recall: MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
Howmedica Osteonics Corp.