[Recalled] Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200 (Catalog Number: 8700-001070-1) Software Version: Version 2.0.1 Product Description: The AutoPulse Resuscitat
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200 (Catalog Number: 8700-001070-1) Software Version: Version 2.0.1 Product Description: The AutoPulse Resuscitation System Model 200 is an automated, portable, battery powered device |
|---|---|
| Brand / manufacturer | ZOLL Circulation, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1533-2025 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 04 March 2025 |
| EAN / barcode | 00849111003384 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.