# FDA recall Z-1780-2018

> **MHC Medical Products LLC** · Class II · device recall initiated 2018-04-06.

## Product

EasyTouch (ET) Insulin Syringe 29G 0.5ml ¿" (Item 829555)    Product Usage:  INTENDED FOR INJECTION OF U100 INSULIN ONLY

## Reason for recall

The retail shelf cartons may be labeled with an incorrect lot number.

## Distribution

US Nationwide Distribution in the states of: AR, AZ, CA, FL, GA, IL, IN, LA, MA, MI, MO, MS, NC, ND, NH, NJ, NV, NY, OH, PA, SC, TN, TX, VA, WA, WI, WV, and Puerto Rico.

## Key facts

- **Recall number:** Z-1780-2018
- **Recalling firm:** MHC Medical Products LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2018-04-06
- **Report date:** 2018-05-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cincinnati, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1780-2018

## Citation

> AI Analytics. FDA recall Z-1780-2018. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-1780-2018. Source: US FDA. Licensed CC0.

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