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.
13,791 stored notices, reported between Jun 20, 2012 and Oct 28, 2026. Newest first.
Reported Jul 8, 2026
Medtronic Harmony Delivery Catheter System
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Heart Valves Division
FDA (openFDA device enforcement)
Reported Jul 8, 2026
SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe, Piston
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mentor Texas LP
FDA (openFDA device enforcement)
Reported Jul 8, 2026
RayCare 2024A SP1. Oncology Information Systems.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2026
GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel, Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2026
ARTIS icono biplane. Model Number: 11327600.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
FDA (openFDA device enforcement)
Reported Jul 8, 2026
GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2026
A M S, ALIGNED MEDICAL SOLUTIONS, DSAEK Pack-RX, Pack Number AMS12394B, surgical convenience kit
High riskUsing this product could cause serious injury, illness or death — stop using it now.Windstone Medical Packaging, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Dual Hose with CPC Connectors…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000434. Introducer Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abiomed, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US Retail Sensor/Transmitter 1-pack…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dexcom, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2026
GE Healthcare AW Server 3.2 ext.6.5; Radiological Image Processing System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems SCS
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Da Vinci ASSY, PSS, SP1098, Part Number: 380601
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IPG Medical Corporation
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Medline Convenience Kits: 1) DYNJ905503F, Model Number: CV ANESTHESIA - ROOM SET UP; 2) DYNJ905503G, Model Number: CV…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medline Industries, LP
19 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Octopus Evolution Tissue Stabilizer, Model TS2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfm Medical Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2026
INZONE DETACHMENT SYSTEM, REF: M00345100950
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Surgify Halo, 3.0 mm, Extendable, Model/Catalog Number: 30.000.SEE.U2; drills, burrs, trephines & accessories (simple,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Surgify Medical Oy
18 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2026
TMJ Bilateral Implants, REF: CHG020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TMJ Solutions Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2026
VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventec Life Systems, 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.