# FDA recall Z-0030-2022

> **Contamac Solutions, Inc.** · Class II · device recall initiated 2021-07-27.

## Product

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

## Reason for recall

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

## Key facts

- **Recall number:** Z-0030-2022
- **Recalling firm:** Contamac Solutions, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-07-27
- **Report date:** 2021-10-13
- **Termination date:** 2023-06-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Grand Junction, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0030-2022

## Citation

> AI Analytics. FDA recall Z-0030-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0030-2022. Source: US FDA. Licensed CC0.

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