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Use caution Medical device recall · FDA · Published March 12, 2018

Hamilton-C2 Ventilator Battery Gauge May Show Higher Charge Than Actual

Hamilton Medical recalls C2 Ventilators due to battery gauge potentially showing higher charge than actual. This could lead to unexpected shutdowns during critical care. Affected units have serial numbers and were sold in hospitals.

🇺🇸 FDA recall #Z-1371-2018Medical deviceHamilton Medical ›
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Recalling firmHamilton Medical AGvia Crusch 8 · Bonaduz, Switzerland
✎ GovInfoNow plain-language explainer

Hamilton Medical is recalling its C2 Ventilator Units because the battery fuel gauge might show a higher charge level than what's actually available after two and a half years. This could cause the ventilator to shut down unexpectedly during critical medical care. Read more at govinfonow.com/recall/71728-hamilton-c2-ventilator-battery-gauge-may-show-higher-charge-than.

Source Summary by GovInfoNow · govinfonow.com/recall/71728-hamilton-c2-ventilator-battery-gauge-may-show-higher-charge-than · Updated August 21, 2026 · FDA enforcement record: FDA #Z-1371-2018

Cite this page

“Hamilton-C2 Ventilator Battery Gauge May Show Higher Charge Than Actual.” GovInfoNow, updated August 21, 2026. https://govinfonow.com/recall/71728-hamilton-c2-ventilator-battery-gauge-may-show-higher-charge-than. Based on FDA recall #Z-1371-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1371-2018%22&limit=1).

The FDA announced on March 12, 2018, that Hamilton Medical AG is recalling the Hamilton-C2 Ventilator Unit. The battery fuel gauge may indicate a higher charge than available after two and a half years of use.

How to tell if you have it

  • Hamilton Medical
  • Hamilton-C2 Ventilator Unit
  • Product No. 160001
  • All Serial Numbers

The hazard

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

Context

GovInfoNow's records show Hamilton Medical AG has 11 other recalls on record since March 9, 2018. Other recent recalls of similar products include GE Healthcare Carestation Anesthesia System Power Board Recall (Nov. 14, 2025), Baxter Blue Ventilator Adapter Module Recall (Feb. 18, 2026), and GE Healthcare Carestation Anesthesia Systems May Shut Down During Power Outages (Nov. 14, 2025).

How to tell if you have this one

Check for the Hamilton-C2 Ventilator Unit with serial numbers. These units were sold in hospitals and intended for adult, pediatric, and neonatal patients.

  • Brand
    Hamilton Medical
  • Category
    Medical device
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • 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, Spain, SRI Lanka, Sudan, Suriname, Sweden, Sweden, Switzerland, Syria, Taiwan, Tajikistan, Thailand, Trinidad & Tobago, Tunisia, Turkey, UAE, Uganda, UK , Ukraine, Uruguay, Venezuela, Vietnam, and Yemen.
Recall numberProduct, codes & lots
Z-1371-2018Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and neonates in the hospital.; Product No. 160001 All Serial Numbers.
Z-1372-2018Hamilton-C3 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and neonates in the hospital.; Product No. 160005 All Serial Numbers
Based on the official FDA remedy

What to do — step by step

  1. Check Battery Gauge

    Verify the battery gauge reading against the actual battery status to ensure it doesn't show a higher charge than available.

Where it went and when

Where it was distributed

Distributed in 29 states and Puerto Rico, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: yesVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: not listedWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: yesSDIowa: not listedIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFLPuerto Rico: yesPR

FDA 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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Colorado, Florida, Georgia, Hawaii, Illinois, Indiana, Kentucky, Massachusetts, Michigan, Minnesota, Missouri, Montana, Nebraska, Nevada, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington.

Recall timeline

FDA published this recall 37 days after the firm started it.

1. Firm started the recall: Mar 12, 201812. FDA classified it Class II: Apr 12, 201823. Published in FDA’s Enforcement Report: Apr 18, 201832018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-1371-2018 (March 12, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1371-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on August 21, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA