MAUDE Adverse Event Report: COLOPLAST A/S PED FOLYSIL CATH 3ML CH08/5; SILICONE FOLEY CATHETER,

Model Number AA61081002

Device Problems Deflation Problem (1149); Difficult to Remove (1528)

Patient Problem Inflammation (1932)

Event Date 04/29/2017

Event Type  malfunction  

Manufacturer Narrative

Device received (b)(6) 2017 for evaluation.Without the benefit of examination and testing, coloplast is precluded from commenting on the condition of the device or the cause of the occurrence.Should additional facts prompt us to alter or supplement any information of conclusions contained in the original mdr or in any prior supplemental reports, a follow-up report will be submitted.Without the benefit of examination and testing, coloplast is precluded from commenting on the condition of the device or the cause of the occurrence.Should additional facts prompt us to alter or supplement any information of conclusions contained in the original mdr or in any prior supplemental reports, a follow-up report will be submitted.On (b)(6) 2017: report was delayed due to an esg issue.Tickets (b)(4) were opened on (b)(6) 2017 and not resolved until (b)(6) 2017.

Event Description

According to the available information, at the time of withdrawal of the catheter (48 hours after having placed it in the patients' body), the deflation of balloon was performed but the catheter remained blocked in the urethral meatus.According to the nurse, it seemed like the balloon was not enough deflated.The catheter had to be pulled to be withdrawn, an inflammation of the penis was reported.Did they tried to inflate/deflate the balloon ? - yes several times.The balloon was empty ? yes, it was thick but no more fluid in the balloon.

Manufacturer Narrative

This follow-up mdr is created to document the evaluation of the returned product: a used folysil catheter with a white valve printed "3 ml-04819790" was received for evaluation.At visual examination, it was noted that the balloon is deflated and hang loose.It was disinfected it and inflated with 3cc of air and no balloon anomaly was observed.It was deflated it and the balloon is ok.It is the remanence issue.The ifu sh2115 provides, in such situation, recommendations to follow during removal.The rmf identified the described risk which is considered acceptable with the recommendations within the ifu.Our clinical assessment estimates that the entrapped folysil catheter as a result of balloon cuffing has required a new surgical intervention under general anesthesia in one case which is a severity parameter rated level 3 according to our current risk management procedure (b)(4).Based on the above, this complaint is not confirmed as a product defect, the root cause is due to user.

• Brand Name: PED FOLYSIL CATH 3ML CH08/5
• Type of Device: SILICONE FOLEY CATHETER,
• Manufacturer (Section D): COLOPLAST A/S; holtedam 1; humlebaek, 3050 ; DA 3050
• Manufacturer (Section G): COLOPLAST A/S MANUFACTURING FRANCE SAS; 9 avenue edmond rostand; sarlat-la-caneda, 24206 ; FR 24206
• Manufacturer Contact: christine buckvold ; 1601 west river road north; minneapolis, MN 55411 ; 6123024982
• MDR Report Key: 6681622
• MDR Text Key: 78849633
• Report Number: 9610711-2017-00018
• Device Sequence Number: 1
• Product Code: EZL
• UDI-Device Identifier: 03600040126974
• UDI-Public: 03600040126974
• Combination Product (y/n): N
• PMA/PMN Number: K013174
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,health professional
• Type of Report: Initial,Followup
• Report Date: 11/08/2017

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: AA61081002
• Device Catalogue Number: AA61081002
• Device Lot Number: 5193878
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 06/08/2017
• Was the Report Sent to FDA?: No
• Initial Date Manufacturer Received: 05/15/2017
• Initial Date FDA Received: 06/30/2017
• Supplement Dates Manufacturer Received: 05/15/2017
• Supplement Dates FDA Received: 11/08/2017
• Was Device Evaluated by Manufacturer?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Outcome(s): Other