Contamac Solutions, Inc.: Medical Device Recall in 2021 - (Recall #: Z-0030-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35 Single-use 10ml ampoules (360ml), UDI:00850012123002

Product Classification:

Class II

Date Initiated: July 27, 2021

Date Posted: October 13, 2021

Recall Number: Z-0030-2022

Event ID: 88529

Reason for Recall:

Contact lens solution may contain foreign material

Status: Terminated

Product Quantity: 104335 vials

Code Information:

Lot Number: FOE

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated