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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: C.R. BARD, INC. (COVINGTON) -1018233 ROCHESTER MEC SPIRIT SHEATH STYLE 2 POP 29MM 30BX; MALE EXTERNAL CATHETER

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C.R. BARD, INC. (COVINGTON) -1018233 ROCHESTER MEC SPIRIT SHEATH STYLE 2 POP 29MM 30BX; MALE EXTERNAL CATHETER Back to Search Results
Model Number 37302
Device Problems Nonstandard Device (1420); Appropriate Term/Code Not Available (3191)
Patient Problems No Consequences Or Impact To Patient (2199); No Known Impact Or Consequence To Patient (2692)
Event Type  malfunction  
Manufacturer Narrative
The investigation is still in progress.Once the investigation is complete a supplemental report will be filed.The information provided by bard represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bard.The device was not returned.
 
Event Description
It was reported that the adhesive on the male external catheter was strong, therefore it was difficult to remove the male external catheter.No medical intervention was reported.
 
Event Description
It was reported that the adhesive on the male external catheter was strong, therefore it was difficult to remove the male external catheter.No medical intervention was reported.
 
Manufacturer Narrative
The device was not returned for evaluation.The device history record was reviewed and found nothing that could have caused or contributed to the reported event.The instructions for use state the following: "pop-on¿ self-adhering male external catheter, wideband¿ self-adhering male external catheter, spirit® style 2 / style 3 hydrocolloid adhesive sheath.En description/indication: the self-adhering male external catheter is designed for the management of male urinary incontinence.Contraindication do not use on irritated or compromised skin.Precaution: do not use if allergic reaction occurs.For good hygiene, change catheter daily.Use of a single device for longer periods than 24 hours may increase the risk of complications.Directions: to apply: wash penis with mild soap and warm water.Dry thoroughly.Trim pubic hair if necessary.Open package at perforation.To remove plastic insert, squeeze catheter at the top of the white cone and pull to release.Unroll self-adhering catheter over penis.Gently squeeze the catheter to properly seal adhesive to the skin.Connect to collection bag.Important: wear time may be significantly reduced if adhesive is not properly sealed to the skin.Directions: to remove, gently roll catheter off the penis.Note: if necessary, apply a warm wet compress (such as a wet washcloth) around the catheter to help loosen the adhesive.Caution: consult accompanying documents use by units manufacturer authorized representative not made with natural rubber latex non-sterile manufacturer: c.R.Bard, inc.Covington, ga 30014 usa (800) 526-4455 www.Bardcare.Com bard limited, forest house crawley, west sussex uk rh11 9bp +44 1293 527 888." the device was not returned.
 
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Brand Name
ROCHESTER MEC SPIRIT SHEATH STYLE 2 POP 29MM 30BX
Type of Device
MALE EXTERNAL CATHETER
Manufacturer (Section D)
C.R. BARD, INC. (COVINGTON) -1018233
8195 industrial blvd
covington GA 30014
MDR Report Key7408043
MDR Text Key105252770
Report Number1018233-2018-01106
Device Sequence Number1
Product Code NNX
UDI-Device Identifier00801741071188
UDI-Public(01)00801741071188
Combination Product (y/n)N
PMA/PMN Number
EXEMPT
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer,other
Type of Report Initial,Followup
Report Date 04/23/2018
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received04/09/2018
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Expiration Date05/28/2022
Device Model Number37302
Device Catalogue Number37302
Device Lot NumberJUBT0838
Was Device Available for Evaluation? No
Date Manufacturer Received04/21/2018
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
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