Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749
Reported: October 27, 2021 Initiated: May 17, 2021 #Z-0146-2022
Product Description
Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749
Reason for Recall
The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
Details
- Recalling Firm
- ADRIA SRL
- Units Affected
- N/A
- Distribution
- The products were distributed to the following US states: NJ and NY.
- Location
- San Giovanni In Persiceto, N/A
Frequently Asked Questions
What product was recalled? ▼
Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749. Recalled by ADRIA SRL. Units affected: N/A.
Why was this product recalled? ▼
The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 27, 2021. Severity: Moderate. Recall number: Z-0146-2022.
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