Recall Z-1276-2023
Datascope Corp. · initiated February 28, 2023
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-00-0800-53, 0998-00-0800-55, and 0998-00-0800-65
Codes / lots: Model Number: 0998-00-0800-31, UDI-DI: 10607567109053; Model Number: 0998-00-0800-32, UDI-DI: 10607567111117; Model Number: 0998-00-0800-33, UDI-DI: 10607567109008; Model Number: 0998-00-0800-35, UDI-DI: 10607567109107; Model Number: 0998-00-0800-45, UDI-DI: 10607567108421; Model Number: 0998-00-0800-52, UDI-DI: 10607567108438; Model Number: 0998-00-0800-53, UDI-DI: 10607567108391; Model Number: 0998-00-0800-55, UDI-DI: 10607567108414; Model Number: 0998-00-0800-65, UDI-DI: 10607567113432; Serial Numbers: CB355244F2, CB355245F2, CB356759G2, CB356760G2, CB351303D2 CB355431F2 CB355432F2 CB355433F2 CB355434F2 CB355435F2 CB356761G2 CB356762G2 CB356763G2 CB356764G2 CB356765G2 CB351313D2 CB352952E2 CB352953E2 CB355240F2 CB355241F2 CB355242F2 CB355243F2 CB356766G2 CB356767G2 CB356768G2 CB356769G2 CB356770G2 CH351787D2 CH352224D2 CH352225D2 CH352228D2 CH352280E2 CH352283E2 CH352284E2 CH352287E2 CH352289E2 CH352290E2 CH352297E2 CH352298E2 CH353439E2 CH353443E2 CH353445E2 CH353448E2 CH353451E2 CH353454E2 CH353795F2 CH353796F2 CH353797F2 CH353798F2 CH353799F2 CH353801F2 CH353802F2 CH353803F2 CH353804F2 CH353805F2 CH353806F2 CH353807F2 CH353808F2 CH353809F2 CH353810F2 CH353811F2 CH353812F2…
Reason for recall
There is an issue related to the Safety Disk not meeting a performance requirement that may impact Intra-Aortic Balloon catheter (IAB) displacement volume. This potential failure of an impacted Safety Disk may lead to slightly reduced IAB inflation during therapy or a reduction in the degree of augmentation provided to the patient during therapy.
FDA-determined cause: Under Investigation by firm
Action taken
An URGENT MEDICAL DEVICE CORRECTION dated 2/28/23 was sent to customers. User Actions to be taken: A review of our records indicate that you may have a Cardiosave IABP at your facility with an affected Safety Disk or affected spare Safety Disks or PIM assembly installed recently into Cardiosave IABP. 1. Please examine your inventory immediately to determine if you have any Cardiosave IABPs with the affected Safety Disks and/or PIM, or any affected Safety Disk and/or PIM assembly spare parts, per attachment 1. 2. You may continue to use any affected IABPs until replacement parts are installed. Please keep in mind the potential health risks cited above, particularly with prolonged heart rates above 100 beats per minute for three consecutive hours. When transporting patients outside the hospital environment, consider using an unaffected console if available. 3. Should you have any unused affected spare parts of the Safety Disk or PIM Assembly in your inventory, please remove them from areas of use and contact your local Datascope/Getinge Customer Service department at 888-9GETUSA (888 943-8872) to request a return authorization (RMA) and shipping instruction to return the affected product for credit. 4. If you installed an affected spare part into one of your IABPs the Safety Disk will need to be replaced. 5. If you purchased spare parts and they are no longer in your inventory and you are unsure of their location, please contact Getinge Service. Getinge Service will schedule an on-site visit to inspect your IABP/(s) at no cost to your facility. 6. Should you have any affected Cardiosave IABPs you will be contacted by a Getinge Service Representative to schedule an on-site visit to replace the Safety Disk, free of charge. You can also arrange a visit by a Getinge trained or authorized service technician by contacting Getinge Technical Support at (888) 943-8872 (select option 4,2,1), Monday through Friday, between the hours of 8:00 a.m. and 6:00 p.m. (Eastern Time Zone
Details
- Recall number
- Z-1276-2023
- Initiated
- February 28, 2023
- Posted by FDA
- March 22, 2023
- Product code
- DSP – System, Balloon, Intra-Aortic And Control
- Quantity
- 391 total IABPs
- Distribution
- Distribution list not yet provided.
- Recalling firm
- Datascope Corp., Mahwah, NJ
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-1277-2023 Class II | Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Numbers Model Numbers…There is an issue related to the Safety Disk not meeting a performance requirement that may impact… | 02/28/2023Open, Classified |
| Z-1278-2023 Class II | Cardiosave Intra-Aortic Balloon Pump (IABP) Safety Disk, Model Number 0202-00-0140There is an issue related to the Safety Disk not meeting a performance requirement that may impact… | 02/28/2023Open, Classified |
| Z-1279-2023 Class II | Cardiosave Intra-Aortic Balloon Pump (IABP) Pneumatic Interface Module (PIM) , Model…There is an issue related to the Safety Disk not meeting a performance requirement that may impact… | 02/28/2023Open, Classified |