FDA Medical devices recall ·
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution recall
- Recall number
- Z-1956-2025
- Date
- (initiated May 15, 2025)
- Company / brand
- Contamac Solutions, Inc.
806 Kimball Ave, Grand Junction, CO, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 17,273 cartons (604,555 ampoules)
- Hazard tags
- Sterility
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Why was it recalled?
Contact lens insertion solution may lack sterility.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI: 00850012123002/ Lot: HFH, HGC, HGI, HGN, HKF, HKK
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: Arizona California Colorado Florida Illinois Indiana Kansas Kentucky Louisiana Maine Michigan North Carolina New Jersey New York Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina Texas Utah Virginia Washington Wisconsin
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1956-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.