medical LOW RISK Updated 2025-12-24

Datascope Corp. recalls Cardiosave Rescue

See all recalls from Datascope Corp. →

Recalled Product

Cardiosave Rescue

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Hazard / Issue

The IFU addendum updates the Vibration and Shock Table to reference the correct standards.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Model: 0998-00-0800-83; UDI-DI: 10607567108407; Serial Numbers: All;

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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Search Amazon for Cardiosave Rescue →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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