CROSSER CTO RECANALIZATION CATHETERS CRUS6A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-13 for CROSSER CTO RECANALIZATION CATHETERS CRUS6A manufactured by Bard Peripheral Vascular, Inc..

Event Text Entries

[177969960] The lot number was provided for both malfunctions and lot history reviews were done. The device has been returned for evaluation for one of the two malfunctions; the evaluation identified detachment. The device has not been returned for the second malfunction; the investigation is inconclusive for detachment as no objective evidence has been provided to confirm any alleged deficiency with the device. Based upon the available information, the definitive root cause is unknown. The devices are labeled for single use.
Patient Sequence No: 1, Text Type: N, H10


[177969961] This report summarizes two malfunctions. A review of the reported information indicated that model crus6a recanalization catheter allegedly experienced a detachment. This information was received from various sources. Both malfunctions involved patients with no reported consequences. One patient was reported as a (b)(6)-year-old male; all other patient details were not provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020394-2020-00190
MDR Report Key9582066
Date Received2020-01-13
Date of Report2020-01-13
Date Mfgr Received2019-12-31
Date Added to Maude2020-01-13
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJUDITH LUDWIG
Manufacturer Street1415 W. 3RD STREET
Manufacturer CityTEMPE AZ 85281
Manufacturer CountryUS
Manufacturer Postal85281
Manufacturer Phone4803032689
Manufacturer G1C.R. BARD, INC. (GFO)
Manufacturer Street289 BAY ROAD
Manufacturer CityQUEENSBURY NY 12804
Manufacturer CountryUS
Manufacturer Postal Code12804
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCROSSER CTO RECANALIZATION CATHETERS
Generic NameRECANALIZATION CATHETER
Product CodePDU
Date Received2020-01-13
Model NumberCRUS6A
Catalog NumberCRUS6A
Lot NumberGFDP3807
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerBARD PERIPHERAL VASCULAR, INC.
Manufacturer Address1625 W 3RD ST. TEMPE AZ 85281 US 85281


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-13

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