Z-1956-2025 Class II Ongoing
FDA device recall Z-1956-2025 was initiated by Contamac Solutions, Inc. on May 15, 2025 and is designated Class II. Reason for recall: Contact lens insertion solution may lack sterility. The recall status is ongoing. Affected quantity: 17,273 cartons (604,555 ampoules).
Recall Details
- Product Type
- Devices
- Report Date
- June 18, 2025
- Initiation Date
- May 15, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 17,273 cartons (604,555 ampoules)
Product Description
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Reason for Recall
Contact lens insertion solution may lack sterility.
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.
Code Information
UDI: 00850012123002/ Lot: HFH, HGC, HGI, HGN, HKF, HKK