Akreos, SKU: AO60P0300. Akreos intraocular lenses
FDA Recall Z-2451-2025 · Posted 2025-08-26
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Recalling FirmBausch & Lomb Surgical, Inc.
Recall StatusOpen, Classified
Product CodeHQL
Date Initiated2025-06-06
Product Quantity2
Reason for Recall
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.
Firm Action
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.
Root Cause
Process control
Distribution Pattern
US: AZ, CA
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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