Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in packages with unacceptable...
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 Amendia, Inc directly.
Affected Products
Dual Stylet Needle, Part Number 812-11R-15 The guide wire is passed through the cannulated handle of the Dual Stylet Needles and pressed into the bone
Quantity: 1078 units
Why Was This Recalled?
The rods are packaged in packages with unacceptable seals. In some cases, the integrity of the seal is compromised by channels or voids.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Amendia, Inc
Amendia, Inc has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report