MAUDE Adverse Event Report: C.R. BARD INC. (COVINGTON) -1018233 LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE; URIPLAN BED BAG

Catalog Number	150619
Medical Device Problem Code	Restricted Flow rate (1248)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/28/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The investigation is still in progress.Once the investigation is complete a supplemental report will be filed.This report references a us equivalent device.The us udi equivalent for this product number is used.H11: section a through f - the information provided by bd represents all 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 bd.
Event or Problem Description
It was reported that, the bed bag was attached to a stand on the floor so it should have drained as normal.Carer tried to pass some water through the bag with the valve open, unfortunately this did not help either and liquid would still got stuck in the tube.There was another problem with one bag, the valve of one bag when first opened would not move at all even with a lot of force so it could not be used.
Event or Problem Description
It was reported that, the bed bag was attached to a stand on the floor so it should have drained as normal.Carer tried to pass some water through the bag with the valve open, unfortunately this did not help either and liquid would still got stuck in the tube.There was another problem with one bag, the valve of one bag when first opened would not move at all even with a lot of force so it could not be used.
Additional Manufacturer Narrative
The reported event was inconclusive because this investigation did not result in any additional findings, and no sample was available for evaluation.The instructions for use were reviewed and found to be adequate.A review of the device history record did not show any problems or conditions that would have contributed to the reported issue.Correction: d.This report references a us equivalent device.The us udi equivalent for this product number is used.H11: section a through f - the information provided by bd represents all 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 bd.
Additional Manufacturer Narrative
The reported event was inconclusive because this investigation did not result in any additional findings, and no sample was available for evaluation.The labeling is found to be adequate.A review of the device history record did not show any problems or conditions that would have contributed to the reported issue.No additional actions can be taken at this time.Correction: d.This report references a us equivalent device.The us udi equivalent for this product number is used.H11: sections a through f - the information provided by bd represents all 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 bd.
Event or Problem Description
It was reported that, the bed bag was attached to a stand on the floor so it should have drained as normal.Carer tried to pass some water through the bag with the valve open, unfortunately this didn't help either and liquid would still got stuck in the tube.There was another problem with one bag, the valve of one bag when first opened would not move at all even with a lot of force so it couldn't be used.

• Brand Name: LEG BAG WITH FLIP-FLO VALVE, NO STRAPS, 19 OZ., STERILE
• Common Device Name: URIPLAN BED BAG
• Manufacturer (Section D): C.R. BARD INC. (COVINGTON) -1018233; 8195 industrial blvd; covington GA 30014
• Manufacturer (Section G): C.R. BARD INC. (COVINGTON) -1018233; 8195 industrial blvd; covington GA 30014
• Manufacturer Contact: xeeroy rada ; 8195 industrial blvd; covington, GA 30014 ; 7707846100
• MDR Report Key: 22715309
• Report Number: 1018233-2025-06498
• Device Sequence Number: 21313290
• Product Code: FAQ
• UDI-Device Identifier: 00801741050831
• UDI-Public: (01)00801741050831(11)250206(17)291130(10)NGJZ2592
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,Consumer
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 10/16/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Lay User/Patient
• Device Catalogue Number: 150619
• Device Lot Number: NGJZ2592
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/28/2025
• Supplement Date Received by Manufacturer: 10/08/2025; 10/16/2025
• Initial Report FDA Received Date: 08/05/2025
• Supplement Report FDA Received Date: 10/15/2025; 10/20/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 02/06/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown