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Browse Device Recalls

3 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 3 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.

Medical Device Recalls

Browse 3 FDA device recalls.

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DateProductReasonClassFirm
Nov 15, 2012 Viterion TeleHealth Monitor Model Number V500; Product Codes 08832984 (US) an... Viterion telehealth monitors do not transmit "HI" (above the meter's measurable range) and "LO" (... Class II Viterion TeleHealthcare Llc
Nov 15, 2012 Viterion TeleHealth Monitor Model Number V100, Product Codes 09377512 (US) an... Viterion telehealth monitors do not transmit "HI" (above the meter's measurable range) and "LO" (... Class II Viterion TeleHealthcare Llc
Nov 15, 2012 Viterion TeleHealth Monitor Model Number V100-BGM, Product Code 81842478 (US... Viterion telehealth monitors do not transmit "HI" (above the meter's measurable range) and "LO" (... Class II Viterion TeleHealthcare Llc

Frequently Asked Questions

When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.

All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.

Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.