Contamac Nutrifill Lens Solution Recall: Foreign Material Risk
Contamac recalls preservative-free lens insertion solution due to potential foreign material. Affected products include 35ml ampoules with specific lot numbers. Consumers should check labels for UDI and lot codes.
Lower-risk recall
Contact lens solution may contain foreign material
Contact the company
What happened, in plain English
Contamac is recalling preservative-free lens insertion solutions that may contain foreign material. This could cause eye irritation or injury if used without proper cleaning. Read more at govinfonow.com/recall/62148-contamac-nutrifill-lens-solution-recall-foreign-material-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/62148-contamac-nutrifill-lens-solution-recall-foreign-material-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0030-2022
Cite this page
“Contamac Nutrifill Lens Solution Recall: Foreign Material Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62148-contamac-nutrifill-lens-solution-recall-foreign-material-risk. Based on FDA recall #Z-0030-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0030-2022%22&limit=1).
Why it’s dangerous
The solution may contain foreign material that could irritate or damage the eye during lens insertion. This risk is low but could cause discomfort or injury if the material is present.
Who’s affected
People who use Contamac Nutrifill lens insertion solutions for contact lenses. Those with sensitive eyes or recent lens wear are at slightly higher risk.
How to tell if you have this one
Check for the product name: Nutrifill Scleral, Hybrid, or Gas Permeable Lens Insertion Solution. Look for the UDI code 00850012123002 and lot number FOE on the packaging.
- Brand
Contamac- Category
Medical device
What to do — step by step
Check Product Label
Look for the UDI code 00850012123002 and lot number FOE on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 48 states.
FDA distribution: “US Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY.…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA terminated this recall 22 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this product safe to use?
The recall states the solution may contain foreign material, so it's not recommended for use until the remedy is followed.
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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-0030-2022 (July 27, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0030-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 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.