STAAR AQ Cartridge-FP recall
STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.
Why was STAAR AQ Cartridge-FP recalled?
The STAAR AQ Cartridge-FP may malfunction and may crack during loading or delivery of the IOL (Intraocular Lenses).
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?
1281706, 1282812
- Product
- STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses.
- Recalling firm
- Staar Surgical Co.
- Quantity
- 2,612 units
- Distribution
- US
- Recall date
- June 22, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)