Recall Z-1232-2023
Datascope Corp. · initiated February 7, 2023
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
Cardiosave Rescue. Model Number: 0998-00-0800-83.
Codes / lots: Model Number: 0998-00-0800-83. UDI-DI: 10607567108407. All serial numbers.
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.
FDA-determined cause: Equipment maintenance
Action taken
Firm notified customers on February 7, 2023, in an Urgent Medical Device Correction letter which discussed four issues in total - this issue was Issue #4. Customers were instructed to contact their Datascope/Getinge service representative if they observe any visual damage to the O-ring installed as part of the quick disconnect fitting. Datascope/Getinge is currently updating the annual Preventive Maintenance instruction to include replacement of the quick disconnect fitting O-ring. If you have any questions, please contact your Datascope/Getinge representative or call the Datascope/Getinge Technical Support at 1-888-943-8872, options 4, 2, 1, Monday through Friday, between the hours of 8:00 a.m. and 6:00 p.m. (Eastern Time Zone). On 11/04/2025 the recall was expanded, and consignees were notified via letter. The notification was for awareness to the update of Datascope s preventative maintenance in the IFU addendum, which was provided to consignees. The IFU Addendum contains an updated Schedule B Preventive Maintenance Schedule which calls for the Quick Disconnect Fitting O-Ring to be replaced and to lubricate the console release latch every 12 months or 2500 hours. The Service Manual has contained this update to Preventive Maintenance for the Helium O-Ring since June 2023. Consignees were instructed to review the IFU Addendum and local Preventive Maintenance Schedule and update their Preventive Maintenance schedule accordingly.
Details
- Recall number
- Z-1232-2023
- Initiated
- February 7, 2023
- Posted by FDA
- March 6, 2023
- Product code
- DSP – System, Balloon, Intra-Aortic And Control
- Quantity
- 47 units (44 US, 3 OUS)
- Distribution
- Nationwide US distribution. Worldwide international distribution.
- Recalling firm
- Datascope Corp., Mahwah, NJ
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-1231-2023 Class II | Cardiosave Hybrid Intra-Aortic Balloon Pump. Model Numbers: D998-00-0800-31…Firm has received reports of damaged, worn, or torn O-rings on the Cardiosave Pump Console quick disconnect… | 02/07/2023Open, Classified |