ARROW IPN000308Recalls & reported problems
Teleflex Incorporated · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30801902043413), received between Nov 19, 2018 and Nov 19, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Alarm System” (1 report).
29 other recalls cover devices cleared under the same FDA submission (K060309); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Device Alarm System1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 19, 2018Device Alarm System; Device Alarm System
IT WAS REPORTED THAT THE USER CALLED THE DEALER'S CALL CENTER TO REPORT A PURGE 3 ALARM THAT OCCURRED DURING USE. THE INTRA-AORTIC BALLOON PUMP (IABP) COULD NOT DETECT AN ELECTROCARDIOGRAM. AS A RESULT, THE IABP WAS REPLACED BY A BACK-UP ONE. THERE WAS NO PATIENT DEATH, SERIOUS INJURY OR COMPLICATIONS REPORTED. PATIENT OUTCOME REPORTED AS GOOD.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8084870 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K060309. One submission often covers many models, so check the product and lot details in each record.
- Z-0429-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT2 WAVE, REF IAP-0500 (IPN000320), cardiac pump
- Z-0445-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400F (IPN000306), cardiac pump
- Z-0448-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500E (IPN000322), cardiac pump
- Z-0450-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500F (IPN000323), cardiac pump
- Z-0444-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400E (IPN000305), cardiac pump
- Z-0447-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500D (IPN000321), cardiac pump
- Z-0452-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500J (IPN000325), cardiac pump
- Z-0456-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500J (IPN000334), cardiac pump
- Z-0449-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500EX (IPN000322), cardiac pump
- Z-0454-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500SV (IPN000327), cardiac pump
- Z-0446-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT 2 IABP, REF IAP-0400J (IPN000308), cardiac pump
- Z-0455-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-05001 (IPN000333), cardiac pump
- Z-0431-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT 2 WAVE, REF IAP-0535 (IPN000329), cardiac pump
- Z-0426-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT 2 IAPB, REF IAP-0400 (IPN000302), cardiac pump
- Z-0451-2023 · Oct 17, 2022 · Open, ClassifiedArrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500I (IPN000324), cardiac pump
…and 14 more.
Other System, balloon, intra-aortic and control devices
- CARDIOSAVE HYBRID, TYPE B PLUG 0998-00-0800-53Datascope Corp. · System, Balloon, Intra-Aortic And Control21 recalls39 deaths10,316 reports
- CS300 Intra-Aortic Balloon Pump, English, 110V 0998-00-3023-53Datascope Corp. · System, Balloon, Intra-Aortic And Control12 deaths3,164 reports
- CARDIOSAVE HYBRID W/ E/F PLUG 0998-00-0800-55Datascope Corp. · System, Balloon, Intra-Aortic And Control20 recalls8 deaths1,686 reports
- CARDIOSAVE HYBRID, TYPE I PLUG 0998-00-0800-45Datascope Corp. · System, Balloon, Intra-Aortic And Control20 recalls5 deaths1,181 reports
- CARDIOSAVE HYBRID, TYPE G PLUG 0998-00-0800-52Datascope Corp. · System, Balloon, Intra-Aortic And Control19 recalls2 deaths1,157 reports
- SENSATION PLUS 8Fr. 50cc IAB & Accessories (w/Pressure Tubes, No Stylet) 0684-00-0576-01Datascope Corp. · System, Balloon, Intra-Aortic And Control2 recalls33 deaths1,541 reports
- CARDIOSAVE RESCUE 0998-00-0800-83Datascope Corp. · System, Balloon, Intra-Aortic And Control26 recalls167 reports
- CARDIOSAVE HYBRID, 3.1 EDITION 0998-00-0800-65Datascope Corp. · System, Balloon, Intra-Aortic And Control20 recalls3 deaths456 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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