FOLEY CATHETER, 400 SERIES 8 FR 81-080408

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2016-09-01 for FOLEY CATHETER, 400 SERIES 8 FR 81-080408 manufactured by Deroyal Industries, Inc..

Event Text Entries

[53718902] Investigation summary an internal complaint (b)(4) was received reporting that a foley catheter with a temperature sensor (81-080408) failed during use. The customer reported the catheter started leaking after less than six weeks of use. This report is one of seven total filed by the reporting customer in reference to the finished good number. According to the initial complaint report, these incidents occurred over a period of several months, and the customer chose to file them at one time in a batch. No lot numbers were provided, and a sample was available for only one of the seven reported incidents. For this incident, a defective sample was received. A shipping inquiry by box identification showed that four cases of finished good (b)(4) were ordered by the reporting customer in 2013 and shipped on july 11, 2013. The lot number shipped to the customer was 32608900, which was manufactured july 2, 2013. Review of this work order shows no discrepancies that would have contributed to the reported issue. The finished good assembly consists of the following raw materials that are assembled as detailed below: raw material part number 74-12088w (foley catheter wire supplied by (b)(4)) is received at the manufacturing plant. After receiving, a connector is molded to the wire set and a continuity test is conducted to ensure the thermistor chip has not had any affectation. The raw material is converted to part number 74-12088cr (molded foley catheter wire set) and shipped to (b)(4). Once (b)(4) has received the product, the part is converted into part number 74-12089 (foley catheter 8 fr) and shipped to the plant in (b)(4) for packaging. It is here the part number is converted to the finished good part number of 81-080408. The silicone catheter portion of this device is supplied by (b)(4). Therefore, a supplier corrective action request (scar) was issued to the vendor on august 29, 2016. The investigation is ongoing at this time. When new and critical information is received, this report will be updated.
Patient Sequence No: 1, Text Type: N, H10


[53718903] A foley catheter with a temperature sensor was leaking from the middle of the tubing at about the height where plaster was placed for fixation. The catheter was placed less than six weeks ago. The leaking catheter was removed and replaced with a new one.
Patient Sequence No: 1, Text Type: D, B5


[62584489] Root cause: the catheter is supplied by (b)(4), and therefore, a supplier corrective action request (scar) was issued to (b)(4). In scar response, (b)(4) stated, during its manufacturing process, every batch of catheters undergoes tensile strength testing to detect weak shaft-funnel connections. In this case, the batch number is unknown, and therefore, (b)(4) was unable to check the tensile strength results. The complaint part number is an 8 french catheter, which is a thin shaft of 2. 7 mm in diameter. If the shaft is pulled with excessive force, it can be torn off of the tunnel. (b)(4) states it is unable to confirm the complaint as the shaft could have been torn following excessive force during use. Corrective action: in its scar response, (b)(4) indicated a corrective action has not been taken. Investigation summary an internal complaint ((b)(4)) was received reporting that a foley catheter with a temperature sensor ((b)(4)) failed during use. The customer reported the catheter started leaking after less than six weeks of use. This report is one of seven total filed by the reporting customer in reference to the finished good number. According to the initial complaint report, these incidents occurred over a period of several months, and the customer chose to file them at one time in a batch. No lot numbers were provided, and a sample was available for only one of the seven reported incidents. For this incident, a defective sample was received. Pictures of the defective catheter were sent to the supplier for evaluation. A shipping inquiry by box identification showed that four cases of finished good (b)(4) were ordered by the reporting customer in 2013 and shipped on july 11, 2013. The lot number shipped to the customer was 32608900, which was manufactured july 2, 2013. Review of this work order shows no discrepancies that would have contributed to the reported issue. The finished good assembly consists of the following raw materials that are assembled as detailed below: * raw material part number 74-12088w (foley catheter wire supplied by (b)(4)) is received at the manufacturing plant. After receiving, a connector is molded to the wire set and a continuity test is conducted to ensure the thermistor chip has not had any affectation. The raw material is converted to part number 74-12088cr (molded foley catheter wire set) and shipped to (b)(4). * once (b)(4) has received the product, the part is converted into part number 74-12089 (foley catheter 8 fr) and shipped to the plant in (b)(4) for packaging. It is here the part number is converted to the finished good part number of 81-080408. The two most recent work orders for raw material part 74-12088cr were reviewed and no rejects were reported during the manufacturing process. The last shipment of raw material 74-12088cr was sent to (b)(4) in 2014. Because the catheter is supplied by (b)(4), a supplier corrective action request (scar) was issued to the vendor on august 29, 2016, and a due date of october 12, 2016, was assigned. A response was not received on this date. Follow up attempts were made and a response was received november 25, 2016. The failure mode and effects analysis (fmea) was reviewed and it was determined no updates are needed at this time. Preventive action: in its scar response, (b)(4) indicated a preventive action has not been taken at this time. The investigation is complete at this time. If new and critical information is received, this report will be updated.
Patient Sequence No: 1, Text Type: N, H10


[62584490] A foley catheter with a temperature sensor was leaking from the middle of the tubing at about the height where plaster was placed for fixation. The catheter was placed less than six weeks ago. The leaking catheter was removed and replaced with a new one.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2320762-2016-00018
MDR Report Key5921465
Report SourceUSER FACILITY
Date Received2016-09-01
Date of Report2016-12-06
Date of Event2016-08-02
Date Mfgr Received2016-08-02
Date Added to Maude2016-09-01
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 ContactSARAH BENNETT
Manufacturer Street200 DEBUSK LANE
Manufacturer CityPOWELL TN 37849
Manufacturer CountryUS
Manufacturer Postal37849
Manufacturer Phone8653626112
Manufacturer G1DEROYAL INDUSTRIES, INC.
Manufacturer Street1595 HIGHWAY33 SOUTH
Manufacturer CityNEW TAZEWELL TN 37825
Manufacturer CountryUS
Manufacturer Postal Code37825
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFOLEY CATHETER, 400 SERIES 8 FR
Generic NameCATHETER, UPPER URINARY TRACT
Product CodeEYC
Date Received2016-09-01
Returned To Mfg2016-08-02
Catalog Number81-080408
Lot NumberNOT PROVIDED
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDEROYAL INDUSTRIES, INC.
Manufacturer Address1595 HIGHWAY 33 SOUTH NEW TAZEWELL TN 37825 US 37825


Patients

Patient NumberTreatmentOutcomeDate
10 2016-09-01

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