Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
8mm FlexDex Needle Driver Recalled by FlexDex Inc. Due to The firm is reinforcing the IFU instructions: "Do...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact FlexDex Inc. directly.
Affected Products
8mm FlexDex Needle Driver, Product Code FD-335 ND
Quantity: 273
Why Was This Recalled?
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.
Where Was This Sold?
Distribution information not available.
About FlexDex Inc.
FlexDex Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report