# FDA recall Z-1956-2025

> **Contamac Solutions, Inc.** · Class II · device recall initiated 2025-05-15.

## Product

Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution

## 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.

## Key facts

- **Recall number:** Z-1956-2025
- **Recalling firm:** Contamac Solutions, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-15
- **Report date:** 2025-06-18

- **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-1956-2025

## Citation

> AI Analytics. FDA recall Z-1956-2025. Retrieved 2026-08-01 from https://api.ai-analytics.org/recall/Z-1956-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
