Summary
The FDA issued a Class II for Cardiosave Rescue. Model Number: 0998-00-0800-83. by Datascope Corp.. Reason: Firm has received reports of damaged, worn, or torn O-rings on the Cardiosave Pump Console quick disconnect fitting, which results in helium tank leak.
Details
Source
Device Recall
External ID
Z-1232-2023
Action Date
2023-03-15
Status
Ongoing
Category
device
Product Description
Cardiosave Rescue. Model Number: 0998-00-0800-83.
Lot/Code Info: Model Number: 0998-00-0800-83. UDI-DI: 10607567108407. All serial numbers.
Quantity Affected: 47 units (44 US, 3 OUS)
Reason for Recall
Firm has received reports of damaged, worn, or torn O-rings on the Cardiosave Pump Console quick disconnect fitting, which results in helium tank leaks. If the helium supply is depleted, therapy will be interrupted.
Distribution
Nationwide US distribution. Worldwide international distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-07
Company
Mahwah, NJ
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 137 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Datascope Corp. has 58 FDA actions in our database, including 58 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Datascope Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Datascope Corp. have FDA actions?
Datascope Corp. has 58 FDA actions in our database, including 58 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1232-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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