MAUDE Adverse Event Report: C.R. BARD, INC. (COVINGTON) -1018233 BARD® DRAIN BAG FOLEY TRAY WITH BARDEX® ALL-SILICONE CATHETER; FOLEY CATHETER TRAY

Model Number	897516
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
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.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.
Event or Problem Description
It was reported that there was a hole in the packaging of the tray.
Additional Manufacturer Narrative
Received 1 foley catheter tray in open packaging.The reported event was confirmed as cause unknown.During visual inspection, it was noted that the package had a hole from the outside to the inside.The csr wrap, package and the tray were all damaged in the same direction.The received sample shows evidence that perforate from outside to inside.The inner components were not damaged.The root cause of damage in tray could not be determined.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: "visually inspect the product for any imperfections or surface deterioration prior to use.If package is opened or if any imperfection or surface deterioration is observed, do not use." (b)(4).
Event or Problem Description
It was reported that there was a hole in the packaging of the tray.

• Brand Name: BARD® DRAIN BAG FOLEY TRAY WITH BARDEX® ALL-SILICONE CATHETER
• Common Device Name: FOLEY CATHETER TRAY
• Manufacturer (Section D): C.R. BARD, INC. (COVINGTON) -1018233; 8195 industrial blvd; covington GA 30014
• MDR Report Key: 7067993
• Report Number: 1018233-2017-06171
• Device Sequence Number: 19147519
• Product Code: EZL
• UDI-Device Identifier: 00801741025020
• UDI-Public: (01)00801741025020
• Combination Product (Y/N): N
• Initial Reporter State: LA
• Initial Reporter Country: US
• PMA/510(K) Number: K040504
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: other,user facility
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 02/02/2018

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: Health Professional
• Device Expiration Date: 10/31/2019
• Device Model Number: 897516
• Device Catalogue Number: 897516
• Device Lot Number: NGBU3420
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/14/2017
• Initial Date Received by Manufacturer: 11/08/2017
• Supplement Date Received by Manufacturer: 01/29/2018
• Initial Report FDA Received Date: 11/29/2017
• Supplement Report FDA Received Date: 02/02/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1