Boston Foundation For Sight recalls specific BostonSight SCLERAL Lens models with errors in sagittal height or haptics. Affected units have unique serial numbers and UDI numbers listed in the recall notice.
Select orders of lenses were manufactured with errors impacting sagittal height, haptics, or both.
Boston Foundation For Sight is recalling certain BostonSight SCLERAL Lenses due to manufacturing errors that could affect sagittal height or haptics. This means the lenses might not fit properly or function as intended, potentially causing discomfort or vision issues.
The lenses were manufactured with errors in sagittal height or haptics, which are critical components for proper fit and function. These errors could lead to improper lens placement or reduced effectiveness, potentially causing discomfort or vision problems.
People who own or use the recalled BostonSight SCLERAL Lenses with the specific serial numbers listed in the recall notice are most at risk. These lenses were manufactured with errors in sagittal height or haptics.
Check the serial numbers and UDI numbers listed in the recall notice. Affected units include specific serial numbers across multiple UDI numbers as detailed in the record.
Identify your lens's serial number and UDI number to see if it matches the affected units listed in the recall notice.
No, only specific lenses with the listed serial numbers and UDI numbers are affected.
Check the serial number and UDI number on your lens against the list of affected units provided in the recall notice.
The recall notice does not specify a remedy, so you should contact Boston Foundation For Sight directly for further instructions.
We’ve drafted a message you can send Boston Foundation For Sight to request your refund or repair — edit it as you like.
Subject: Recall Z-2190-2025 — Boston Foundation For Sight Boston Foundation For Sight Hello, I own a Boston Foundation For Sight that is covered by recall Z-2190-2025 from Boston Foundation For Sight. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
