Biofinity® Toric Multifocal and XR Toric
Last updated
Summary
Product
Biofinity® Toric Multifocal and XR Toric
Issue
Medical devices - Labelling and packaging
Medical devices - Sterility
What to do
Contact the manufacturer if you require additional information.
Affected products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| Biofinity® Toric Multifocal | More than 10 numbers, contact manufacturer. | BIOFINITY TORIC MULTIFOCAL |
| Biofinity® XR Toric | RD0228875 | BIOFINITY XR TORIC |
| Biofinity® XR Toric | RE0152873 | BIOFINITY XR TORIC |
| Biofinity® XR Toric | RD0227007 | BIOFINITY XR TORIC |
Issue
The lenses may contain lens blisters (packaging) with an incomplete or leaking seal resulting in a potentially unsterile condition. Consumers may experience adverse reactions up to and including ocular infection, should they not detect the seal integrity failure and the lens becomes unsterile prior to use.
Recall start date: June 24, 2025
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Ophthalmology
Companies
Coopervision Manufacturing Limited (Ata Coopervision)
South Point, Southampton, United Kingdom, SO31 4RF
Published by
Health Canada
Audience
General public
Healthcare
Recall class
Type II
Identification number
RA-77673
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