Contamac Contact Lens Solution Recall: Risk of Unsterile Product
Contamac recalls Nutrifill Physiologic formula contact lens insertion solution due to potential lack of sterility. Affected products have specific UDI and lot numbers. Consumers should check their items and contact Contamac for details.
Lower-risk recall
Contact lens insertion solution may lack sterility.
Contact the company
What happened, in plain English
Contamac is recalling its Nutrifill Physi: Contact Lens Insertion solution because it may not be sterile. This could lead to eye infections if used improperly. The recall affects specific product batches with known UDI and lot numbers. Read more at govinfonow.com/recall/52264-contamac-contact-lens-solution-recall-risk-of-unsterile-product.
Source Summary by GovInfoNow · govinfonow.com/recall/52264-contamac-contact-lens-solution-recall-risk-of-unsterile-product · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1956-2025
Cite this page
“Contamac Contact Lens Solution Recall: Risk of Unsterile Product.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52264-contamac-contact-lens-solution-recall-risk-of-unsterile-product. Based on FDA recall #Z-1956-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1956-2025%22&limit=1).
Why it’s dangerous
The contact lens insertion solution may not be sterile, which can cause eye infections if used. This is a potential risk for individuals who rely on the solution for contact lens care.
Who’s affected
People who use Contamac Nutrifill Physiologic formula contact lens insertion solution are affected. Those with the specific UDI and lot numbers listed are most at risk.
How to tell if you have this one
Check the product label for the UDI: 00850012123002 and lot numbers HFH, HGC, HGI, HGN, HKF, HKK. This product is sold under the brand Contamac.
- Brand
Contamac- Category
Medical device
What to do — step by step
Check Product Label
Look for the UDI code 00850012123002 and lot numbers HFH, HGC, HGI, HGN, HKF, HKK on the product label.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 25 states.
FDA distribution: “US Nationwide distribution in the states of AZ, CA, CO, FL, IL, IN, KS, KY, LA, ME, MI, NC, NJ, NY, OH, OK, OR, PA, RI, SC, TX, UT, VA, WA, WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, California, Colorado, Florida, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Michigan, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Texas, Utah, Virginia, Washington, Wisconsin.
Recall timeline
FDA published this recall 34 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-1956-2025 (May 15, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1956-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.