Health product recall

Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses

Last updated

Summary

Product
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalog number
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A -2.25D V00D228
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A -5.25D J003QDG
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A -2.00D J003Q72
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A -7.25D J003QCV
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A 2.00D J003QCD
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A -4.75D J003QD9
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A -3.00D J003QCQ
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A -6.75D J003QBT
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A 2.75D J003QCG
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A -2.50D J003QCM
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A -5.75D J003QDK
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A -7.50D J003QBX
Acuvue® Oasys Max 1-Day Multi-Focal Contact Lenses SENOFILCON A -2.00D J003Q73

Issue

Johnson & Johnson Vision care, Inc. is voluntarily recalling Acuvue® Oasys Max 1-day Multifocal due to a high density of microbubbles (microscopic voids within the contact lens) observed in specific limited lots. Microbubbles will not cause medical harm but may be associated with visual disturbances, particularly in low-light conditions.

Recall start date: June 12, 2025

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Ophthalmology
Companies

Johnson & Johnson Vision Care, Inc.

7500 Centurion Parkway, Jacksonville, Florida, United States, 32256

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-77637

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