Hazard Type

Battery Hazard Recalls

349 product recalls involving battery hazard. Search official CPSC, FDA, and USDA datasets for every recall issued due to this hazard.

349Total Recalls
64Critical
14402.8MUnits Affected
All Recalls

Every Battery Hazard Recall

Sorted by most recent. Click any recall for full details and safety information.

349 recalls
CriticalFDA
Arrow International Inc.
Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400J (IPN000308), cardiac pump
Cardiac Devices·4 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500F (IPN000323), cardiac pump
Cardiac Devices·48 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601(IPN916548), cardiac pump
Cardiac Devices·0 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/AJLA, REF IAP-0701 (IPN917286), cardiac pump
Cardiac Devices·0 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700(IPN917285), cardiac pump
Cardiac Devices·0 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500E (IPN000322), cardiac pump
Cardiac Devices·112 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601(IPN917288), cardiac pump
Cardiac Devices·0 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500D (IPN000321), cardiac pump
Cardiac Devices·39 affected·Oct 17, 2022
RecallFDA
Baxter Healthcare Corporation
Starling Monitor, Product code CMMST5 and Starling Monitor SV, Product code CMM-ST5 (same products); and accessories/spare parts Starlin...
Medical Devices·9,671 affected·Sep 2, 2022
High RiskFDA
Siemens Healthcare Diagnostics, Inc.
Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use in the quantitative determination of iron in human serum and (lithium heparin...
Diagnostic Devices·1,614 affected·Jun 28, 2022
High RiskFDA
Alere San Diego, Inc.
The Cholestech LDX¿ System combines enzymatic methodology and solidphase technology to measure total cholesterol, HDL cholesterol, trigl...
Diabetes Devices·436,990 affected·Jun 24, 2022
High RiskFDA
Siemens Medical Solutions Usa, Inc
Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System
Medical Devices·233 affected·May 24, 2022
High RiskFDA
Medtronic Minimed
MiniMed 640G Insulin Pump (O.U.S. Version)
Diabetes Devices·323,417 affected·May 23, 2022
High RiskFDA
Medtronic Minimed
MiniMed 740G Insulin Pump (O.U.S. Version)
Diabetes Devices·40 affected·May 23, 2022
High RiskFDA
Medtronic Minimed
MiniMed 670G Insulin Pump (U.S. and O.U.S. Version)
Diabetes Devices·279,251 affected·May 23, 2022
High RiskFDA
Medtronic Minimed
MiniMed 720G Insulin Pump (O.U.S. Version)
Diabetes Devices·575 affected·May 23, 2022
High RiskFDA
Medtronic Minimed
MiniMed 780G Insulin Pump (O.U.S. Version)
Diabetes Devices·83,398 affected·May 23, 2022
CriticalFDA
Medtronic Inc
HeartWare Battery, Model #1650DE, a component of the HeartWare Ventricular Assist Device (HVAD) System.
Cardiac Devices·429 affected·May 5, 2022
CriticalFDA
Smiths Medical Asd Inc.
Medfusion Syringe Pump Model: Model 4000-0100-50, Model 4000-0101-249, Model 4000-0101-50, Model 4000-0101-51, Model 4000-0101-78, Model...
Medical Devices·58,671 affected·Apr 18, 2022
CriticalFDA
Ge Healthcare, Llc
Replacement back up batteries distributed on or after April 1, 2019, for CARESCAPE R860, Engstr¿om Carestation and Engstr¿om PRO Ventilat...
Respiratory Devices·88,379 affected·Apr 18, 2022
High RiskFDA
Cardinal Healthcare
Lithium Carbonate Extended-Release Tablets, USP, 300 mg, 100 Tablets per bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., M...
Oral Drugs·1 affected·Jan 26, 2022
RecallFDA
Physio-control, Inc.
HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Cardiac Devices·1 affected·Jan 13, 2022
High RiskFDA
Greiner Bio-one North America, Inc.
greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in t...
Medical Devices·889,200 affected·Dec 9, 2021
High RiskFDA
Ge Healthcare, Llc
GE Vscan Extend, being sold as "Vscan Extend Sector DICOM"
Medical Devices·12,526 affected·Nov 4, 2021
High RiskFDA
Ge Healthcare, Llc
GE Vscan Extend, being sold as "Vscan Extend Dual USB"
Medical Devices·12,526 affected·Nov 4, 2021
High RiskFDA
Ge Healthcare, Llc
GE Vscan Extend, being sold as "Vscan Extend Dual Wi-Fi"
Medical Devices·12,526 affected·Nov 4, 2021
High RiskFDA
Ge Healthcare, Llc
GE Vscan Extend, being sold as "Vscan Extend Sector USB"
Medical Devices·12,526 affected·Nov 4, 2021
High RiskFDA
Ge Healthcare, Llc
GE Vscan Extend, being sold as "Vscan Extend Sector Wi-Fi"
Medical Devices·12,526 affected·Nov 4, 2021
High RiskFDA
Ge Healthcare, Llc
GE Vscan Extend, being sold as "Vscan Extend Console"
Medical Devices·12,526 affected·Nov 4, 2021
High RiskFDA
Ge Healthcare, Llc
GE Vscan Extend, being sold as "Vscan Extend Dual DICOM"
Medical Devices·12,526 affected·Nov 4, 2021
High RiskFDA
Western/scott Fetzer Company
Western Oxytote DTE Digital VIPR System (with D-size cylinder) Model: MNDS-602
Medical Devices·40 affected·Oct 16, 2021
High RiskFDA
Western/scott Fetzer Company
Western Oxytote DTE Digital VIPR System (with E-size cylinder) Model: MNDS-603
Medical Devices·40 affected·Oct 16, 2021
High RiskFDA
Western/scott Fetzer Company
Western Oxytote DTE Digital VIPR (head only) Model: MNDR-600
Medical Devices·4,974 affected·Oct 16, 2021
CriticalFDA
Datascope Corp.
Cardiosave Li-Ion Battery Pack, Part No. 0146-00-0097. Component of the Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) with the belo...
Medical Devices·131 affected·Sep 21, 2021
High RiskFDA
Datascope Corp.
Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-00-0800-34, 0998-0...
Medical Devices·3,969 affected·Sep 8, 2021
High RiskFDA
Philips Ultrasound Inc
Philips Ultrasound, Inc. Sparq, Diagnostic Ultrasound System, REF 795116, 100-240V -, 50/60 Hz, 500 VA, CE2797, Rx Only,
Diagnostic Devices·1 affected·Aug 19, 2021
High RiskFDA
Ge Oec Medical Systems, Inc
OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic and digital spot im...
Surgical Devices·3 affected·Jun 10, 2021
CriticalFDA
Boston Scientific Corporation
INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)
Medical Devices·3,634 affected·Jun 3, 2021
CriticalFDA
Boston Scientific Corporation
INTUA CRT-P, Model Numbers: a) V272 b) V273 c) W273
Medical Devices·1,707 affected·Jun 3, 2021
CriticalFDA
Boston Scientific Corporation
INGENIO DR EL (pacemakers), Model Numbers: a) J174 b) J177 c) K174 (added 7/15/2021) d) K184 (added 7/15/2021) e) K187 (added 7/15/2021)
Cardiac Devices·40,224 affected·Jun 3, 2021
RecallFDA
Mindray Ds Usa, Inc. Dba Mindray North America
3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115-047566-00 /115-060044-00) and TM80 Te...
Medical Devices·804 affected·May 27, 2021
High RiskFDA
Cardinal Health Inc.
LITHIUM CARB 150MG 100; NDC/UPC 54252625; RX; CAPSULES
Oral Drugs·298 affected·Mar 15, 2021
High RiskFDA
Biotronik Inc
BIOTRONIK Ilestro 7 VR-T, DF-1, REF 383578, UDI: 04035479125349 - Product Usage: intended to provide ventricular tachycardia pacing and v...
Cardiac Devices·1,000 affected·Mar 8, 2021
High RiskFDA
Biotronik Inc
BIOTRONIK Ilestro 7 VR-T DX, DF-1, REF 383594, UDI: 04035479125509 - Product Usage: intended to provide ventricular tachycardia pacing an...
Cardiac Devices·3,664 affected·Mar 8, 2021
High RiskFDA
Biotronik Inc
BIOTRONIK INVENTRA 7, HF-T QP DF4 IS4, REF 393012, UDI: 04035479129286 - Product Usage: intended to provide ventricular tachycardia paci...
Cardiac Devices·702 affected·Mar 8, 2021
High RiskFDA
Biotronik Inc
BIOTRONIK ILIVIA NEO 7 DR-T DF-1 ProMRI, REF 429529, UDI: 04035479156749 - Product Usage: intended to provide ventricular tachycardia pac...
Cardiac Devices·98 affected·Mar 8, 2021
High RiskFDA
Biotronik Inc
BIOTRONIK ITREVIA 7, VR-T DF-4, REF 393041, UDI: 04035479129569 - Product Usage: intended to provide ventricular tachycardia pacing and v...
Cardiac Devices·670 affected·Mar 8, 2021
High RiskFDA
Biotronik Inc
BIOTRONIK Ilestro 7 DR-T, DF-1, REF383562, UDI: 04035479125189 - Product Usage: intended to provide ventricular tachycardia pacing and ve...
Cardiac Devices·0 affected·Mar 8, 2021