Reported Dec 16, 2020 · Terminated
MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during…
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 TROCAR KIT 23G S - Product Usagefor use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery
- RefMTK 23S
- Lot codes and dates
- Lot CodesV180077300
- Exp Date2020/10 and V200009500
- EXp Date2022/03
- Amount recalled
- 6 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.
Free recall alerts
Get alerted about new Mani, Inc. - Kiyohara Facility recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.