Reported Apr 23, 2025 · Ongoing
Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog Number: Model 200…
ZOLL Circulation, Inc.
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: ZOLL Circulation, Inc. · 2000 Ringwood Ave · San Jose, CA · 95131-1728
Is this the product you have?
- Brand NameAutoPulse
- NXT Resuscitation System Product NameAutoPulse
- NXT Platform Model/Catalog NumberModel 200 (Catalog
- Number8700-001070-1)
- Software VersionVersion 2.0.1
- Product DescriptionThe AutoPulse Resuscitation System Model 200 is an automated, portable, battery powered device that compresses the chest of an adult human as an adjunct to manual CPR
- ComponentN/A
- Lot codes and dates
- UDI(01) 00849111003384/Serial
- number
79 of 79 codes
117911681178118411881197110911101126116611691152119912021111118511981203120612081211121211721182113011281129118911831131113411911186119211701173117511801174117611871177111611651118111911931138113911451146114711481149115011531155115911611162
- Amount recalled
- 91
Where it was sold
Why it was recalled
Stop using this product now
AutoPulse NXT Resuscitation System may not provide adequate chest compressions or may stop compressions due to code FC1060.
Using this product could cause serious injury, illness or death — stop using it now.
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