MANI Infusion Cannula recall
MANI Infusion Cannula 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery Ref: MTC…
Why was MANI Infusion Cannula recalled?
Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Codes: V180082900, Exp. Date: 2020/11 and V190000100, Exp Date: 2020/12
- Product
- MANI Infusion Cannula 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery Ref: MTC…
- Recalling firm
- Mani, Inc. - Kiyohara Facility
- Quantity
- 60 units (US)
- Distribution
- US Nationwide distribution in the state of MO.
- Recall date
- December 16, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)