Akreos, SKU: AO60P0300. Akreos intraocular lenses
Recall
- Recall Number
- Z-2451-2025
- Event Number
- 97232
- Firm
- Bausch & Lomb Surgical, Inc.
- FEI Number
- 1119279
- Product Code
- HQL
- Status
- Open, Classified
- Root Cause
- Process control
- Initiated
- June 6, 2025
- Posted
- August 26, 2025
- Address
- 21 N Park Place Blvd, Clearwater, FL, 33759-3917
Description
Akreos, SKU: AO60P0300. Akreos intraocular lenses
An off-power error was identified, which resulted in a diopter of 16, rather than the intended 3 diopter. Implantation of affected intraocular lens could result in functional visual impairment or reduction in visual acuity which could result in the need for optical or surgical correction.
6/6/2025, recall notices were emailed to customers who were asked to do the following: 1) Check your inventory, quarantine, and do not use the IOL from this impacted lot. 2) Provide this notice to all those who need to be aware within your organization or to any organization where the potentially affected devices have been transferred (as appropriate). Also, please transfer this notice to other organizations on which this action has an impact (as appropriate). Please maintain awareness of this notice and resulting action for an appropriate period to ensure effectiveness of the corrective action. 3) Complete and return the acknowledgement form via email to [email protected] For questions regarding this notice, please call firm at 1-800-338-2020, Option 9.
US: AZ, CA
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