FDA-Device2021-10-27Class II
Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745
ADRIA SRL
Hazard
The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
Sold states
The products were distributed to the following US states: NJ and NY.
Affected count
N/A
Manufactured in
Via Modena 46, Societa Unipersonale, San Giovanni In Persiceto, N/A, Italy
Products
Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0145-2022Don't want to check this manually?
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