Reported Oct 27, 2021 · Terminated
Herniatome, 17G x 15cm, Lumbar Type with with 20ga-30cm Introducer, Model Number 5091715
Adria Srl
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: ADRIA SRL · Via Modena 46 · San Giovanni In Persiceto, N/A · N/A
Is this the product you have?
Herniatome17G x 15cmLumbar Type with with 20ga-30cm IntroducerModel Number 5091715
- Lot codes and dates
- Lot NumberAD0316/20
- Amount recalled
- N/A
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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