medical Class II Updated 2018-05-02

Howmedica Osteonics Corp. recalls Knee Prosthesis, Sterile, Single-Use devices Product Usag

Recalled Product

Knee Prosthesis, Sterile, Single-Use devices Product Usage: The knee system devices are intended for use in revision total knee arthroplasty to alleviate pain and restore function

Hazard / Issue

Firm became aware that the specific product/lot combinations referenced above may contain the incorrect size implant from what is labeled on the box.

Issued by

FDA

Distribution: Affected products were sent to three medical facilities. Affected product will be returned to the manufacturer for disposition.
Lot/Code Info: Catalog 5521-B-300, lot code ATV7IA Catalog 5521-B-400, lot code ATY40A
View official government recall

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