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
High RiskFDA
Zyno Medical Llc
Z-800 Infusion System. Model/Catalog Number: Z-800, Z-800F, Z-800W, Z-800WF. The Z-800 Infusion system is intended to provide intrav...
Medical Devices·34,994 affected·Oct 18, 2024
High RiskFDA
Caire, Inc.
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-2.
Respiratory Devices·26 affected·Oct 4, 2024
High RiskFDA
Smith & Nephew Medical, Ltd.
RENASYS EDGE The RENASYS¿ EDGE pump is indicated for patients who would benefit from a suction pump (NPWT), as it may promote wound he...
Medical Devices·1,589 affected·Oct 2, 2024
RecallCPSC
Amazon.com And Papablic.com From July 2023 Through April 2024 For About $150.
Papablic Infant Swings Recalled Due to Suffocation Hazard; Violations of Federal Regulations for Infant Sleep Products; Imported by Shenzhen Two Pony
Toys·2,700 affected·Aug 1, 2024
High RiskFDA
Smiths Medical Asd, Inc.
smiths medical CADD-Solis Li-ion Rechargeable Battery Packs AC adapter, Model Number REF 21-0270-25, for use with the CADD-Solis infusion...
Medical Devices·156,400 affected·Jun 26, 2024
High RiskFDA
Securitas Healthcare Llc
Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living areas...
Medical Devices·1,268 affected·Jun 20, 2024
CriticalFDA
Baxter Healthcare Corporation
Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20...
Respiratory Devices·2,510 affected·May 29, 2024
CriticalFDA
Optumhealth Care Solutions Llc
Optum Nimbus II Plus, Model number AAA-00170; Ambulatory Infusion Pump
Medical Devices·208 affected·Apr 18, 2024
High RiskFDA
Ge Healthcare Finland Oy
CARESCAPE Canvas 1000, Model Numbers: a) 5865770; b) 5865770-01040169; c) 5865770-01054142; d) 5865770-01054696; e) 5865770-0105469...
Medical Devices·9,267 affected·Apr 5, 2024
High RiskFDA
Ge Healthcare Finland Oy
CARESCAPE Canvas Smart Display, Model Numbers: a) 5514418, b) 5514418 / MAEP2, c) 5514418-01059642, d) 5514418-01080402, e) 55144...
Medical Devices·547 affected·Apr 5, 2024
High RiskFDA
Ge Healthcare Finland Oy
CARESCAPE B850 Model Numbers: a) MBC303, Model Numbers: 1) 2078633-001, 2) 2078633-010, 3) 2078633-012, 4) 2078633-017, 5) 20786...
Medical Devices·25,268 affected·Apr 5, 2024
High RiskFDA
Ge Healthcare Finland Oy
CARESCAPE B650: Model Numbers: a) MBB313, Model Numbers: 1) 2095801-001, 2) 2095801-001-01018416, 3) 2095801-001-01023150, 4) 209...
Medical Devices·54,800 affected·Apr 5, 2024
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051
Medical Devices·1 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-000061, Part Number V15-2-000067
Medical Devices·1 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022
Medical Devices·8 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-001960, Part Number: V15-7-000026
Medical Devices·2 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-001373, Part Number V15-7-000002
Medical Devices·1 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-001956, Part Number V15-7-000021
Medical Devices·1 affected·Sep 29, 2023
High RiskFDA
Physio-control, Inc.
LIFEPAK 15, REF: 99577-001255, Part Number V15-2-001602
Medical Devices·5 affected·Sep 29, 2023
High RiskFDA
Securitas Healthcare Llc
Arial Water Resistant Pendant with Long Wristband, Models: 59362 and 2560-59362; mobile patient alarm
Medical Devices·49 affected·Sep 25, 2023
High RiskFDA
Securitas Healthcare Llc
Arial Water Resistant Pendant with Wristband, Models: 59361 and 2560-59361; mobile patient alarm
Medical Devices·2,691 affected·Sep 25, 2023
High RiskFDA
Securitas Healthcare Llc
Arial Water Resistant Pendant with Neck Lanyard, Models: 59360 and 2560-59360; mobile patient alarm
Medical Devices·1,235 affected·Sep 25, 2023
High RiskFDA
Smiths Medical Asd Inc.
Portex Pro-Vent Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, REF 4599P-1
Medical Devices·31,900 affected·Sep 6, 2023
CriticalFDA
Datascope Corp.
Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-31, 0998-UC-0800-31, 0998-00-0800-32, 0998-00-0800-33, 099...
Medical Devices·9,175 affected·Jul 31, 2023
CriticalFDA
Datascope Corp.
Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
Medical Devices·9,175 affected·Jul 31, 2023
High RiskFDA
Baxter Healthcare Corporation
GEM FLOW COUPLER Monitor, PN 5156-00000-011
Medical Devices·122 affected·Jun 19, 2023
CriticalFDA
Draeger Medical, Inc.
Oxylog 3000 Plus emergency and transport ventilator
Respiratory Devices·300 affected·Jun 12, 2023
CriticalFDA
Datascope Corp.
Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33 0998-00-0800-34 0...
Medical Devices·9,174 affected·Jun 5, 2023
CriticalFDA
Datascope Corp.
Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85
Medical Devices·9,174 affected·Jun 5, 2023
CriticalFDA
Icu Medical Inc
Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Number 30010
Medical Devices·28,656 affected·Mar 22, 2023
CriticalFDA
Icu Medical Inc
ASM Replacement Battery, Component Number SUB0000864
Medical Devices·9,984 affected·Mar 22, 2023
CriticalFDA
Icu Medical Inc
ASM Replacement Battery, Component Number SUB0000594
Medical Devices·344 affected·Mar 22, 2023
High RiskFDA
Siemens Healthcare Diagnostics, Inc.
Atellica IM Cortisol 50T (Material Number 10995538), 250T (Material Number 10995537), and REF 250T (Material Number 11206248). In vitro d...
Diagnostic Devices·34,746 affected·Mar 16, 2023
High RiskFDA
Siemens Healthcare Diagnostics, Inc.
ADVIA Centaur Cortisol 50T (Material Number 10994924), ADVIA Centaur Cortisol 250T (Material Number 10994926), and ADVIA Centaur Cortisol...
Diagnostic Devices·18,961 affected·Mar 16, 2023
High RiskFDA
Tobii Dynavox Llc
Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device used for ambulatory people with disabilities. Catalog #: 75...
Medical Devices·3,924 affected·Feb 24, 2023
RecallCPSC
Independent Diving Stores Nationwide And Online At Www.diveblu3.com And Www.amazon.com From October 2021 Through November 2022 For Between $1,900 And $2,700.
BLU3 Recalls Nomad Battery-Powered Tankless Diving Systems Due to Drowning Hazard for Divers
Batteries & Power·1,300 affected·Dec 22, 2022
High RiskFDA
Siemens Healthcare Diagnostics, Inc.
ADVIA Centaur XP and ADVIA Centaur XPT Anti-HBe2 (aHBe2) 50T- In vitro diagnostic immunoassay for the qualitative detection of antibodies...
Diagnostic Devices·158 affected·Dec 22, 2022
High RiskFDA
Getinge Usa Sales Inc
Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System (Product Code 6887900)
Medical Devices·65 affected·Nov 7, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT2 WAVE REFURBISHED, REF IAP-0535X (IPN000329), cardiac pump
Cardiac Devices·1 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-05001 (IPN000333), cardiac pump
Cardiac Devices·1 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT 2 WAVE, REF IAP-0535 (IPN000329), cardiac pump
Cardiac Devices·81 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700 (IPN001112), 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 (IPN916549), cardiac pump
Cardiac Devices·0 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT2, REF IAP-0435 (IPN000312), cardiac pump
Cardiac Devices·12 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/EMEA, REF IAP-0600 (IPN001108), cardiac pump
Cardiac Devices·0 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500SV (IPN000327), cardiac pump
Cardiac Devices·15 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500NL (IPN000326), cardiac pump
Cardiac Devices·4 affected·Oct 17, 2022
CriticalFDA
Arrow International Inc.
Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT 2 IAPB, REF IAP-0400 (IPN000302), cardiac pump
Cardiac Devices·1,394 affected·Oct 17, 2022