ADRIA SRL recalls Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745
The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
Read the official notice →- Date
- 2021-10-27
- Country
- United States
- Brand
- Adria
- Product
- Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745
- Classification
- Class II
- Units
- The products were distributed to the following US states: NJ and NY.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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