Reported Dec 16, 2020 · Terminated
MANI Infusion Cannula 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials…
Mani, Inc. - Kiyohara Facility
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: Mani, Inc. - Kiyohara Facility · Park 8-3 · Utsunomiya, N/A · N/A
Is this the product you have?
- MANI
- Infusion Cannula 23G S - Product Usagefor use in injecting perfusate or aspirating out intraocular
- materials during ophthalmic surgery RefMTC 23S
- Lot codes and dates
- Lot CodesV180082900, Exp
- Date2020/11 and V190000100
- Exp Date2020/12
- Amount recalled
- 60 units (US)
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
- MO
Why it was recalled
Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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