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FDAApril 12, 2017device

Bone Dowell Harvest Tubes

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

The hazard

mislabeled as 8mm tube but it is actually 9 mm in size. A 9mm subcomponent was erroneously substituted and etched as 8mm for the actual 8mm subcomponent part.

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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Bone Dowell Harvest Tubes — Recall Details · AllClear