Reported Aug 21, 2024 · Ongoing
RMU-2000 Automated Chest Compression Device
Defibtech, LLC
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Defibtech, LLC · 741 Boston Post Rd · Guilford, CT · 06437-2714
Is this the product you have?
- RMU-2000 Automated Chest Compression Device
- Lot codes and dates
- UDI-DI00815098020812, 10815098020819 Serial numbers
216 of 216 codes
502001000502000281502000979502000960502000985502000988502000264502000201502000973502000249502000248502000205502000216502000217502000275502000204502000234502000267502000270502000237502000232502000227502000907502000908502000980502000987502000078502000074502000064502000072502000224502000235502000223502000225502000231502000222502000245502000246502000932502000220502000938502000934502000945502000946502000922502000958502000927502000944502000942502000236502000943502000941502000238502000998502000250502000948502000068502000294502000939502000284
- UDI-DI00815098020812, 10815098020819 Serial numbers
- Amount recalled
- 174 US, 37 OUS
Where it was sold
Why it was recalled
Stop using this product now
Problem in the device's motor may cause the device to stop compressions. This may lead to a delay in therapy if the device fails to operate, and could lead to patient injury or death.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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