Medical device recalls
Device recalls are the largest single group in this archive, because the FDA logs corrections and removals as well as outright withdrawals. Many are handled entirely between the manufacturer and a hospital and need nothing from a patient. Each notice states who has to act.
13,634 stored notices, reported between Jun 20, 2012 and Sep 9, 2026. Newest first.
Reported Jan 21, 2026
A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Jan 21, 2026
Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mobius Imaging, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2026
Product Name: Allura Xper FD10C; Model number: 722001;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2026
MAVERICK¿ Measurement Module Spectrometer PN 820-01367 (originally part of a kit PN 820-01519) Finished Goods PN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Repligen Corporation
FDA (openFDA device enforcement)
Reported Jan 21, 2026
CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec LLC
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Impella 5.5 with SmartAssist¿ S2, Impella 5.5 with SmartAssist S2 Set, AU.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abiomed, Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.
High riskUsing this product could cause serious injury, illness or death — stop using it now.AVID Medical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Beckman Coulter UniCel Dxl 600, Part numbers: A71460, A71461, A30260; Immunoassay Method, Troponin Subunit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 14, 2026
BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number: 119695-000, 119629-000, 119630-000,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IMRIS Imaging Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK,OXYGEN,UND CHIN,MED CO OUS ONLY; HUD1035 O2 MASK,MED…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Revogene C. difficile, in vitro diagnostic assay intended for use with the Revogene instrument, Catalog Number 410300
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Philips Incisive CT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare (Suzhou) Co., Ltd.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with streptavidin-coated microparticles and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Securitas Healthcare LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 14, 2026
LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
The Pressio 2 ICP Monitoring System, Model Number PSO-4000; Intracranial Pressure Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sophysa
FDA (openFDA device enforcement)
Reported Jan 14, 2026
The AlignRT InBore system contains six Class 1 lasers which enables the system s cameras to track the patient s…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vision RT Ltd.
FDA (openFDA device enforcement)
Reported Jan 7, 2026
BVI Leos Laser and Endoscopy System. Model Number: OME6000U.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver-Visitec International, Inc.
FDA (openFDA device enforcement)
Reported Jan 7, 2026
Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog Number: 0523-48 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferndale Laboratories, Inc.
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.