FoodJul 5, 2023
Richin Trading Sun Wave Brand Jelly Cup recall — FDA F-1301-2023
Potential choking hazard
Class IFDA: TerminatedRichin Trading Inc.
Latest records
Latest recalls — page 547
The newest recall records with useful source details are listed here.
DrugJul 5, 2023
The Harvard Drug Group Tramadol Hydrochloride Tablets, USP 50 mg, Unit Dose 100-Count recall — FDA D-0878-2023
Packaging defect: blister packaging inadequately sealed.
Class IIFDA: TerminatedThe Harvard Drug Group
VehicleJun 29, 2023
Honda master cylinder recall — NHTSA campaign 23V458000
Honda (American Honda Motor Co.) is recalling certain 2020-2021 Civic, 2020-2023 Ridgeline, 2021-2023 Passport, 2021-2022 Pilot, and 2020 Acura MDX vehicles. The tie rod fastener that…
master cylinderHonda (American Honda Motor Co.)
Medical DeviceJun 28, 2023
CRHF CRT-D DTBA2D4 VIVA XT IS1/DF4 INTL, Model Number DTBA2D4 recall — FDA Z-1737-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRT-D DTBB2Q1 VIVA QUAD S IS4/DF1 INTL, Model Number DTBB2Q1 recall — FDA Z-1747-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRTD DTPA2D1G COBALT XT HF QUAD OUS, Model Number DTPA2D1G recall — FDA Z-1775-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD COBALT VR MRI IS1 DF1, Model Number DVPB3D1 recall — FDA Z-1820-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD-DR DDMB1D4 EVERA MRI XT IS-1/DF4 US, Model Number DDMB1D4 recall — FDA Z-1712-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
Wilson-Cook Medical Hemospray Endoscopic Hemostat: Reference Part Numbers: a) HEMO-7, REF recall — FDA Z-1978-2023
There are potential risks of the Hemospray powder adhering to the distal end of the endoscope, which can result in adhesion of the endoscope to tissue and consequent difficulty or inability…
Class IIFDA: OngoingWilson-Cook Medical Inc.
Medical DeviceJun 28, 2023
CRHF ICD-VR DVAB1D4 VISIA AF US DF4, Model Number DVAB1D4 recall — FDA Z-1790-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRTD CROME HF QUAD MRI IS4 DF4, Model Number DTPC2QQ recall — FDA Z-1788-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD-VR DVAB1D1 VISIA AF US IS1/DF1, Model Number DVAB1D1 recall — FDA Z-1789-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRT-D DTBC2Q1 BRAVA QUAD IS4/DF1 INTL, Model Number DTBC2Q1 recall — FDA Z-1751-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD COBALT XT VR MRI DF4, Model Number DVPA2D4 recall — FDA Z-1819-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD CROME VR MRI DF4, Model Number DVPC3D4 recall — FDA Z-1823-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD EVERA XT DR GOLD CTD, Model Number DDBB1D4G recall — FDA Z-1706-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRTD COBALT XT HF MRI IS1 DF1, Model Number DTPA2D1 recall — FDA Z-1774-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRTD DTPA2D1PX COBALT XT HF QUAD OUS, Model Number DTPA2D1PX recall — FDA Z-1776-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD COBALT VR MRI DF4, Model Number DVPB3D4 recall — FDA Z-1821-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRT-D DTBB1Q1 VIVA QUAD S IS4/DF1 US, Model Number DTBB1Q1 recall — FDA Z-1743-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF ICD-VR DVMC3D4 EVERA MRI S DF4 GLOB, Model Number DVMC3D4 recall — FDA Z-1813-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
CRHF CRTD DTMB1QQ AMPLIA MRI QUAD US DF4, Model Number DTMB1QQ recall — FDA Z-1764-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceJun 28, 2023
Olympus Corporation of the Americas Single Use Repositionable Clip QUICKCLIP PRO 230CM 5/BX recall — FDA Z-1990-2023
Complaints on clip deployment occurring during clinical procedures, leading to hazardous situations where clips fail to achieve their expected function or deploy incorrectly, potentially…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceJun 28, 2023
CRHF CRTD COBALT XT HF QUAD MRI IS4 DF4, Model Number DTPA2QQ recall — FDA Z-1779-2023
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization…
Class IFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories