Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Contamac Recalled by Contamac Solutions, Inc. Due to Contact lens insertion solution may lack sterility.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Contamac Solutions, Inc. directly.
Affected Products
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Quantity: 17,273 cartons (604,555 ampoules)
Why Was This Recalled?
Contact lens insertion solution may lack sterility.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Contamac Solutions, Inc.
Contamac Solutions, Inc. has 2 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report