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Browse Device Recalls

7 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 7 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 7 FDA device recalls.

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DateProductReasonClassFirm
Jul 29, 2025 Chemistry Products LAC Slides. Catalog Number: 8433880. 1 Sales Unit = contai... VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600 Systems are experiencin... Class II Ortho-Clinical Diagnostics, Inc.
Jul 29, 2025 VITROS Chemistry Products LAC Slides. Catalog Number: 8150112. 1 Sales Unit =... VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600 Systems are experiencin... Class II Ortho-Clinical Diagnostics, Inc.
Jul 10, 2024 The VITROS XT Chemistry Products ALB-TP Slides is a single device that contai... The reason for this recall is QuidelOrtho has determined that during normal use the VITROS XT ALB... Class II Ortho-Clinical Diagnostics, Inc.
Apr 9, 2024 VITROS Immunodiagnostic Products Free T3 Reagent Pack-IVD is for the quantita... T3 Reagent Packs used with Free T3 Calibrators may produce positively biased results for patient ... Class II QUIDELORTHO
Apr 9, 2024 VITROS Immunodiagnostic Products Free T3 Calibrators-IVD are for use with Fre... Free T3 Calibrators used with T3 Reagent Packs may produce positively biased results for patient ... Class II QUIDELORTHO
Oct 25, 2023 VITROS Chemistry Products ECO2 Slides-For in vitro diagnostic use only. VITR... Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing that some lots from Coa... Class II Ortho-Clinical Diagnostics, INc.
Aug 9, 2023 Proboscis/Piston Assembly, Part Number J55375, for VITROS 5,1 FS Chemistry Sy... Ortho Clinical Diagnostics (QuidelOrtho) confirmed certain Proboscis/Piston Assemblies manufactur... Class II Ortho-Clinical Diagnostics, Inc.

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.