MAQUET Cardiosave Hybrid IABP Power Cord Incompatible with Brazilian Outlets
Datascope Corp. recalls Cardiosave Hybrid IABP pumps with specific model numbers due to incompatible Brazilian power cord. Affected units may not operate safely in Brazil.
Recall notice
The power cord supplied (Type J plug end) for the Cardiosave Hybrid IABP to Brazil is incompatible with the Brazilian Type N power receptacle.
Contact the company
What happened, in plain English
Datascope Corp. is recalling Cardiosave Hybrid Intra-Aortic Balloon Pumps with model number 0998-XX-0800-32 because the power cord supplied for Brazil doesn't fit Brazilian outlets. This could prevent the pump from working safely in Brazil. Read more at govinfonow.com/recall/58626-maquet-cardiosave-hybrid-iabp-power-cord-incompatible-with-brazilian-outlets.
Source Summary by GovInfoNow · govinfonow.com/recall/58626-maquet-cardiosave-hybrid-iabp-power-cord-incompatible-with-brazilian-outlets · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1462-2023
Cite this page
“MAQUET Cardiosave Hybrid IABP Power Cord Incompatible with Brazilian Outlets.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58626-maquet-cardiosave-hybrid-iabp-power-cord-incompatible-with-brazilian-outlets. Based on FDA recall #Z-1462-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1462-2023%22&limit=1).
Why it’s dangerous
The power cord's plug type (Type J) is incompatible with Brazil's Type N outlets. This means the pump may not connect properly or could cause electrical issues if plugged in.
Who’s affected
Users in Brazil with the specific model number 0998-XX-0800-32 are most at risk as the power cord won't fit their outlets.
How to tell if you have this one
Check for the model number 0998-XX-0800-32 on the pump. The product has specific serial numbers listed in the recall notice.
- Brand
MAQUET- Category
Medical device
What to do — step by step
Check Model Number
Look for the model number 0998-XX-0800-32 on the pump's label.
How this recall unfolded
Recall timeline
FDA published this recall 29 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this dangerous?
The recall indicates potential incompatibility, but the record doesn't describe specific injury risks.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1462-2023 (April 4, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1462-2023 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.