The Sjögren’s Foundation remains dedicated to the safety of Sjögren’s patients and providing you with the information you need to make important health decisions.
On May 15, 2025, Contamac Solutions issued a nationwide voluntary recall of Nutrifill Preservative Free Scleral, Hybrid, and Gas Permeable Lens Insertion Saline Solution (Lots: HFH, HGC, HGI, HGN, HKF, and HKK) distributed between June 16, 2024 and October 28, 2024.
Several consumer complaints were filed describing red, irritated, burning, and painful eyes with some consumers developing infections and corneal ulcers. Upon investigation, quality failures during manufacturing resulted in Contamac Solutions claiming they could not confirm sterility of 605,465 ampoules manufactured within lots HFH, HGC, HGI, HGN, HKF, and HKK.
Consumers should verify if the product is impacted by looking at the lot number. If you have an affected lot, discontinue use immediately. Contact your physician or healthcare provider if you experience any problems related to the use of this product.
Product Reporting and Refund
Consumers can return the remaining product to the point of purchase for a refund. If purchased from Contamac Solutions directly, consumers can request a return by emailing recall [at] contamacsolutions [dot] com (recall[at]contamacsolutions[dot]com) and fill out the Customer Response Form.
For further information on the recall or assistance with the completion of the online report form, please contact:
Toll Free: 1-303-500-0561
Email: recall [at] contamacsolutions [dot] com (recall[at]contamacsolutions[dot]com)
Reporting Adverse Reactions
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
- Complete and submit the report Online
- Regular Mail or Fax: Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
The Sjögren’s Foundation remains dedicated to the safety of Sjögren’s patients and providing you with the information you need to make important health decisions.
On May 15, 2025, Contamac Solutions issued a nationwide voluntary recall of Nutrifill Preservative Free Scleral, Hybrid, and Gas Permeable Lens Insertion Saline Solution (Lots: HFH, HGC, HGI, HGN, HKF, and HKK) distributed between June 16, 2024 and October 28, 2024.
Several consumer complaints were filed describing red, irritated, burning, and painful eyes with some consumers developing infections and corneal ulcers. Upon investigation, quality failures during manufacturing resulted in Contamac Solutions claiming they could not confirm sterility of 605,465 ampoules manufactured within lots HFH, HGC, HGI, HGN, HKF, and HKK.
Consumers should verify if the product is impacted by looking at the lot number. If you have an affected lot, discontinue use immediately. Contact your physician or healthcare provider if you experience any problems related to the use of this product.
Product Reporting and Refund
Consumers can return the remaining product to the point of purchase for a refund. If purchased from Contamac Solutions directly, consumers can request a return by emailing recall [at] contamacsolutions [dot] com (recall[at]contamacsolutions[dot]com) and fill out the Customer Response Form.
For further information on the recall or assistance with the completion of the online report form, please contact:
Toll Free: 1-303-500-0561
Email: recall [at] contamacsolutions [dot] com (recall[at]contamacsolutions[dot]com)
Reporting Adverse Reactions
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Learn More About the Nutrifill Recall by Clicking Below