Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Herniatome Recalled by ADRIA SRL Due to The recalling firm was notified by the contract...
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 ADRIA SRL directly.
Affected Products
Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749
Quantity: N/A
Why Was This Recalled?
The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
Where Was This Sold?
This product was distributed to 2 states: NJ, NY
About ADRIA SRL
ADRIA SRL has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report