Grand Junction, CO, United States
Contamac Solutions, Inc. recalls
2 recalls recorded since 2018, most recently on 15 May 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)1
Terminated or completed1
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 15 May 2025
- Reason
- Contact lens insertion solution may lack sterility.
- 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.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1956-2025
- Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Terminated Class II Medical devices
- Recall started
- 27 July 2021
- Terminated
- 7 June 2023
- Reason
- Contact lens solution may contain foreign material
- 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. OUS: N/A
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0030-2022
- Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.