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 18, 2023
MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheter, Sterile, Single Use, Rx Only: 13.5cm, Straight…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien LP
FDA (openFDA device enforcement)
Reported Jan 18, 2023
COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LLC
FDA (openFDA device enforcement)
Reported Jan 18, 2023
BIOSTOP G BIORESORBABLE CEMENT RESTRICTOR Catalog Numbers: 546308000 (Size 8); 546310000 (Size 10); 546312000 (Size…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Depuy Ireland UC
FDA (openFDA device enforcement)
Reported Jan 18, 2023
DeRoyal ORGAN RECOVERY PACK PGYBK, a) REF 89-9004.09 and b) 89-9004.10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
RSDL (Reactive Skin Decontamination Lotion) Kit, NSN 6505-21-912-5229. Used to remove and/or neutralize chemical…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Emergent Protective Products USA Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Codman Surgical Patties, Part number 801400; SURG PATXRAY 1/2X1/2-200; Lot 6396457
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400, Female Lock - Female Lock Guarded Luer Connector,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.International Medical Industries, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Medline CISION Sterile Blades. Labeled as follows with corresponding Item Number. a. STERILE BLADE NO. 10 CARBON STEEL,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
FDA (openFDA device enforcement)
Reported Jan 18, 2023
RadiaLux Lighted Retractor (Pink), REF: 50-101-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate monitoring during labor. PN:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Philips Trilogy 100 Ventilator, Model Numbers 1054260, 1054096, U1054260, U1054260B, 1054260B, CA1054096B, BT1054260,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2023
cobas infinity central lab, Material Number 07154003001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
IMMULITE 2000 Thyroglobulin (US)- For in vitro diagnostic use with the IMMULITE 2000 Systems Analyzers (IMMULITE 2000/…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Stradis Healthcare Foley Catheter Insertion Tray with preconnected bag and catheter, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stradis Healthcare
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2023
6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems. Ref: CRANI-A Intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2023
VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2023
ActiveAid 922, Shower/Commode Chair
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Altimate Medical, Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2023
Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular paracentesis incisions in cataract procedures. Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver Visitec International, Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2023
BECKMAN COULTER IRISpec CA/CB/CC control, REF 900-7211, For in vitro diagnostic use only.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2023
API LISTERIA 10 STRIPS+10 MEDIA, CATALOG 10300
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
93 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 11, 2023
DeRoyal Tonsillectomy Tray, REF 89-10698.01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2023
Detect Covid-19 Test Product/Model Number: 21205
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Detect Headquarters
FDA (openFDA device enforcement)
Reported Jan 11, 2023
9 Gauge Disposable Trocars with Blunt Pushers for Use with Subcutaneous Implants Part Number: 50134-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ENDO Pharmaceuticals Solutions, 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.