# FDA recall Z-1372-2018

> **Hamilton Medical AG** · Class II · device recall initiated 2018-03-12.

## Product

Hamilton-C3 Ventilator Unit    Intended to provide ventilator support to adults and pediatrics and optionally infants and neonates in the hospital.

## Reason for recall

After two and a half years, the battery fuel gauge may indicate a higher battery charge than what is available.

## Distribution

Worldwide Distribution -- USA, including the states of AZ, CA, CO, FL, GA, HI, IL, IN, KY, MA, MI, MN, MO, MT, NC, ND, NE, NV, OH, OK, PA, SC, SD, TN, TX, UT, VA, VT, and WA; and, the countries of Algeria, Angola, Argentina, Armenia, Australia, Austria, Austria, Azerbaijan, Bangladesh, Belarus, Belgian, Bolivia, Brazil, Bulgaria, Bulgaria, Cambodia, Canada, Chile, China, Colombia, Costa Rica, Croatia, Czechia, Denmark, Dominican. Rep., Ecuador, Egypt, El Salvador, Estland, Finland, France, Gabon, Germany, Greece, Guatemala, Holland, Honduras, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, Kuwait, Latvia, Lebanon, Libya, Lithuania, Malaysia, Maldives, Mauritius, Macedonia, Mexico, Mongolia, Morocco, Myanmar, Nepal, New Zealand, Nigeria, Norway, Oman, Pakistan, Palestine, Panama, Peru, Philippines, Poland, Portugal, Puerto Rico, Romania, Russia, Rwanda, Saudi Arabia, Scotland, Serbia, Seychelles, Slovakia, Slovenia, South Africa, S

## Key facts

- **Recall number:** Z-1372-2018
- **Recalling firm:** Hamilton Medical AG
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2018-03-12
- **Report date:** 2018-04-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bonaduz, Switzerland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1372-2018

## Citation

> AI Analytics. FDA recall Z-1372-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-1372-2018. Source: US FDA. Licensed CC0.

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