medical Class II Updated 2018-05-02

Howmedica Osteonics Corp. recalls Triathlon Revision Knee Catalog #5545-A-301 and Catalog #554

Recalled Product

Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee system devices are sterile, single-use devices intended for us in revision total knee arthroplasty to alleviate pain and restore function.

Hazard / Issue

Customers may receive the incorrect size implant from what is labeled on the box.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Catalog #5545-A-301, lot code ER9WA1A, ER9WA1D, ER9WA1E Catalog #5546-A-601, lot code ER9MA5A
View official government recall

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