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Adria Srl FDA Recalls
3 recalls on file across devices, 0 of them Class I and 0 still open. This firm is not matched to a listed company.
Newest first
Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.
| Product |
|---|
| Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749Class IIMay 17, 2021The recalling firm was notified by the contract sterilizer t |
| Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745Class IIMay 17, 2021The recalling firm was notified by the contract sterilizer t |
| Herniatome, 17G x 15cm, Lumbar Type with with 20ga-30cm Introducer, Model Number 5091715Class IIMay 17, 2021The recalling firm was notified by the contract sterilizer t |