Every recall we track for Defibtech, LLC — 14 in all — plus the complaints and injury reports the public filed about them.
Defibtech recalls DDU-2300 AEDs without Italian language instructions, violating Swiss medical device labeling laws. No action needed for safety, but ensure all three official languages are included.
Defibtech recalls DDU-2200 AEDs sold in Switzerland without Italian language instructions, violating Swiss medical device regulations. Affected units lack Italian translation per Swiss Medical Devices Ordinance.
Defibtech recalls DDU-2450 AEDs sold in Switzerland without Italian language instructions, violating Swiss medical device labeling laws. Affected units must be checked for specific item numbers.
Defibtech recalls DDU-2200 AEDs sold in Switzerland without Italian language instructions, violating Swiss medical device regulations requiring three official languages.
Defibtech recalls DDU-100 and DDU-100E defibrillators due to missing Italian language instructions, violating Swiss medical device labeling requirements.
Defibtech recalls DDP-100 adult defibrillation pads sold in Ireland with unauthorized labels that may appear expired but could cause poor electrical connection during cardiac arrest.
Defibtech recalls pediatric defibrillation pads that may have expired labels appearing valid, risking poor shock delivery during cardiac emergencies. Affected pads were sold in the Irish market with unauthorized labels.
Defibtech recalls RMU-2000 Automated Chest Compression Devices with motor issues that may stop compressions, risking patient injury or death. Affected units have specific serial numbers.
Defibtech recalls DDU-100 AEDs with specific serial numbers due to untested components that may fail during cardiac arrest emergencies.
Defibtech recalls DDU-2400EN Lifeline PRO AEDs with UDI 00815098020270 due to risk of failing to deliver shock during cardiac arrest emergencies. Affected units may not function properly when needed.
Defibtech recalls DDU-2300 Lifeline/ReviveR View AEDs with specific model numbers and serial ranges due to risk of failing to deliver shock during cardiac emergencies.
Defibtech recalls DDU-2450 Lifeline AEDs with specific model numbers and serials due to risk of failing to deliver shock during cardiac arrest emergencies.
