Visitec Anterior Chamber Cannula recall
Visitec Anterior Chamber Cannula, .40x22mm (27Gx7/8in) REF 585006 Cannulae are intended to irrigate and or aspirate ophthalmic solutions and liquids…
Why was Visitec Anterior Chamber Cannula recalled?
Contains a sharp tip needle when the product should contain a blunt tip cannula
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 number: 3079324
- Product
- Visitec Anterior Chamber Cannula, .40x22mm (27Gx7/8in) REF 585006 Cannulae are intended to irrigate and or aspirate ophthalmic solutions and liquids…
- Recalling firm
- Beaver-Visitec International Inc.
- Quantity
- 9970 units
- Distribution
- Nationwide Distribution including AL, CT, IN, NC, NY, TX, and VA.
- Recall date
- June 4, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)