Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
This recall is currently active, issued June 11, 2025. It was issued by Contamac Solutions, Inc..
- Company
- Contamac Solutions, Inc.
- Recall Initiated
- May 15, 2025
- Posted
- June 11, 2025
- Recall Number
- Z-1956-2025
- Quantity
- 17,273 cartons (604,555 ampoules)
- Firm Location
- Grand Junction, CO
- Official Source
- View on FDA website ↗
Reason for Recall
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.
Lot / Code Info
UDI: 00850012123002/ Lot: HFH, HGC, HGI, HGN, HKF, HKK
Root Cause
Process control
Action Taken
On May 15, 2025, Contamac Solutions issued a Urgent Medical Device Recall Notification via Email. In addition, the firm issued a press release concerning the recall on the Contamac Solutions, Inc. eCommerce website . Contamac Solutions ask consignees to take the following actions: 1. Refer to the package label and Product Distribution Information to verify the product is impacted. 2. Immediately quarantine and discontinue use of impacted product 3. Please either return any unused product to Contamac Solutions or destroy and discard the product (i.e. remove vial cap and empty contents before discarding). Please contact recall@contamacsolutions.com to initiate a return. 4. Complete the Customer Response form. If you are having trouble accessing the form, please reach out to recall@contamacsolutions.com for assistance. 5. Provide the recall notification to all those who need to be aware, including others within your organization or to any organization where the affected devices may have been transferred. 6. Distributors - If you have further distributed the product, please provide this recall notification to those distributors and ask them to provide a copy to their customer.