Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos recall
Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos IOL intended for primary implantation in the capsular bag of the eye for the visual correction…
Why was Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos recalled?
Lens was manufactured with incorrect raw material.
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?
Model Numbers(s): AO60 and MI60L
- Product
- Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos IOL intended for primary implantation in the capsular bag of the eye for the visual correction…
- Recalling firm
- Bausch & Lomb Surgical, Inc.
- Quantity
- 336 IOLs (283 IOLs in the US, 53 IOLs outside the US)
- Distribution
- Worldwide Distribution: US (nationwide) and Internationally to: Great Britain, France, Spain, Portugal, Sweden, Russia and Guadeloupe.
- Recall date
- February 26, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)