FDAOctober 10, 2019device

Various temporary devices used during the implantation of the device system: bone fixation plates and screws, drill bits, manual surgical instruments for general use. Item Nos. 0202024301 0202024325 0202024330 0202024342 0202024344 0202024346 0202024360 0202024362 47225806700

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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