FDADecember 22, 2021device
8mm FlexDex Needle Driver, Product Code FD-335 ND
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The firm is reinforcing the IFU instructions: "Do not use if the package is damaged." If upon inspection of the packaging, any damage is observed, including pinholes or tears in the pouch, the product should not be used.
What to do
FDA enforcement status: Terminated
Brands named
flexdex
Recall history
No related federal recalls on record for this brand yet.
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