Contamac Solutions, Inc.: Device Recall
Recall #Z-1956-2025 · 05/15/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1956-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Contamac Solutions, Inc.
- Status
- Ongoing
- Date Initiated
- 05/15/2025
- Location
- Grand Junction, CO, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 17,273 cartons (604,555 ampoules)
Reason for Recall
Contact lens insertion solution may lack sterility.
Product Description
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Distribution Pattern
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.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.