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 Nov 30, 2022
Alinity m System, REF 08N53-002, For In Vitro Diagnostic Use
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
InControl Insulin Syringes, Short Needle, 29 Gauge, 1CC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allison Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
BASIN SET, MEBS42K, general surgical kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Contract Systems, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
Unity Total Knee System. Used for knee prosthesis in total knee replacement
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Corin Ltd.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
eSuction Small Cavity, Model ET2005
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Endo-Therapeutics, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
Hamilton-C6
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hamilton Medical AG
FDA (openFDA device enforcement)
Reported Nov 30, 2022
K-ASSAY IgA Immunoturbidimetric Assay, REF: KAI-013
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kamiya Biomedical Company, LLC
FDA (openFDA device enforcement)
Reported Nov 30, 2022
B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries, Inc. 306
FDA (openFDA device enforcement)
Reported Nov 30, 2022
PAJUNK Continuous Epidural Tray, Tuohy Epidural Needle 17G x 4" with EpiLong Soft Catheter, Closed Tip, 19G, Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pajunk Medical Systems, LP
FDA (openFDA device enforcement)
Reported Nov 30, 2022
regard LAMINECTOMY, NU01140, Item Number 900940; neuro surgery convenience kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ROi CPS LLC
39 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2022
Medfusion Model 4000 Syringe Infusion Pump, with software versions V1.6.0 or V1.6.1 that have implemented the Smart…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE, REF 73-8020, STERILE EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Southmedic, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2022
VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS-IR) Product Number: 174-0012
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Visionsense, Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2022
Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Blue Electric Heating Pad, MB-001
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whele LLC dba Perch
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2022
EasyStand Bantam, with the following sizes. a. Small; b. Extra Small. Used for assisting individual in standing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Altimate Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Hill-Rom Progressa Bed System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Nov 23, 2022
BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for the rapid identification and susceptibility of most…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Superion¿ Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Nov 23, 2022
MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Canadian Hospital Specialties
FDA (openFDA device enforcement)
Reported Nov 23, 2022
CareFusion V.Mueller GENESIS MINI CONTAINER 10-1/2 X 7-1/2" (26.7X19.0CM) 3" (7.6CM) DEEP STERRAD COMPATIBLE, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
16 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Endo Stitch V-Loc 180 Absorbable Reload, Models VLOCA004L, VLOCA006L, VLOCA008L, VLOCA204L, VLOCA206L, VLOCA208L,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 23, 2022
125 series iGO2 Portable Oxygen Concentrator-indicated for the administration of supplemental oxygen. Models: 125D,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeVilbiss Healthcare 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.