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Lifewatch Services, Inc.

Country not established

Devices
1
FDA recalls
3

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Lifewatch Services, Inc. makes

Lifewatch Services, Inc. manufactures the LifeWatch Mobile Cardiac Telemetry 3 Lead LifeWatch MCT 3L, a Class II medical device.

The company is based in the US and its devices are listed in the FDA 510(k) registry.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

FDA recalls3

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 3 recalls initiated by Lifewatch Services, Inc., initiated on 2011-09-26. By recorded status: 3 terminated. The reasons filed fall into these groups: electrical or power. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2011

    • 26 Sep 2011 Z-0206-2012 Unclassified (pre-2012) Terminated LifeWatch received complaints of minor shocks and burns during use of the LifeStar ACT systems with shorts in the leads. Distribution: Nationwide distribution. Submission numbers: K071995, K101639
    • 26 Sep 2011 Z-0207-2012 Unclassified (pre-2012) Terminated LifeWatch received complaints of minor shocks and burns during use of the LifeStar ACT systems with shorts in the leads. Distribution: Nationwide distribution. Submission numbers: K081257, K110499
    • 26 Sep 2011 Z-0208-2012 Unclassified (pre-2012) Terminated LifeWatch received complaints of minor shocks and burns during use of the LifeStar ACT systems with shorts in the leads. Distribution: Nationwide distribution. Submission numbers: K071995, K081257, K101639, K110499

Frequently asked questions

How many devices does Lifewatch Services, Inc. have in the registry?

The registry currently lists 1 device for Lifewatch Services, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lifewatch Services, Inc.'s devices?

Among its 1 most recently registered device, Lifewatch Services, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Lifewatch Services, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Lifewatch Services, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Lifewatch Services, Inc.?

FDA recall records list 3 recalls initiated by Lifewatch Services, Inc., the most recent initiated on 26 Sep 2011. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Lifewatch Services, Inc. in the registry?

The most recently registered devices listed for Lifewatch Services, Inc. include LifeWatch Mobile Cardiac Telemetry 3 Lead LifeWatch MCT 3L.

Generated automatically from registry data and not verified by a human reviewer.