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 Jun 10, 2026
Pediatric care bed; Product Designation: KayserBett IDA;
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kayserbetten GmbH & Co. Kg
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kico Knee Innovation Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oculus Technologies
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
FDA (openFDA device enforcement)
Reported Jun 10, 2026
ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SSC- Surgical Specialties Corporation
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Aligned Medical AMS16835 Fluids Kit RX
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2026
Automated Impella Controller (AIC); Product Code: 0042-0000-US;
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abiomed, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2026
RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U 28-N4-32-164-28U…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bolton Medical Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2026
HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Devicor Medical Products Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2026
GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Information Technologies Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2026
Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) ANESTHESIA TRAY, Medline…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medline Industries, LP
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2026
Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2026
Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.O&m Halyard Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2026
Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 27, 2026
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2026
Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
FDA (openFDA device enforcement)
Reported May 27, 2026
Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported May 27, 2026
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
8 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2026
OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm, 010-107-1007-2/Small 7 Degree 10mm X…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novapproach Spine, LLC
FDA (openFDA device enforcement)
Reported May 27, 2026
Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 27, 2026
Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tangent Endoscopy, LLC
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.