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 Jun 17, 2026
EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Berlin Heart GmbH
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Boston Scientific CSK Electrodes: REF: CSK-TC10, CSK Electrode, STAINLESS STEEL, 10 cm x 28 ga (0.36 mm) REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2026
TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Hintermann Series Talar Implant, Left, Size 2 REF 302112
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DT MedTech, LLC
FDA (openFDA device enforcement)
Reported Jun 17, 2026
MOSAIQ Oncology Information System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Bicarby" Dialysate; Model Numbers: RFP-400-G, RFP-401-G, RFP-402-G, RFP-404-G, RFP-407-G, and RFP-456-G;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Roast Systems Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Allia IGS 3 Pulse angiographic X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HF Acquisition Co. LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Plum Solo Precision IV Pump, 40001-0401
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2026
NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.In2bones USA, LLC
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830
Moderate riskThis product could cause temporary or reversible health problems — stop using it.INSPIREMD Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inter-Med LLC
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medartis AG
FDA (openFDA device enforcement)
Reported Jun 17, 2026
SD LTM 64 PLUS, EEG Amplifier/recorder, Model/Catalog Number: SD LTM 64 PLUS, Software Version: firmware 2021.02,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micromed S.p.A.
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acute Dual Lumen Catheter with Straight…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mozarc Medical US LLC
FDA (openFDA device enforcement)
Reported Jun 17, 2026
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Jun 17, 2026
NexxZr T Multi A3.5 W98-16mm, REF: 745451
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sagemax Bioceramics, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2026
Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mid Scala Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Bionics, LLC
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model/Catalog Number: 555076 Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
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.