MAUDE Adverse Event Report: C.R. BARD, INC. (COVINGTON) -1018233 MAGIC 3 PEDIATRIC CATHETER

Model Number	52808G
Health Effect - Clinical Codes	No Consequences Or Impact To Patient (2199); 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 device was not returned.
Event or Problem Description
It was reported that the patient's mother said the catheter was sometimes harder to insert since the patient was older and moving more.It was unknown if the patient was able to void.
Additional Manufacturer Narrative
The reported event could not be confirmed as no sample was returned for evaluation.A potential root cause for this failure could be catheter is not stiff enough for insertion.The lot number is unknown; therefore, the device history record could not be reviewed.The instructions for use were found adequate and state the following: "inspect the catheter before use.Do not use the product if the device or packaging is damaged." h11:section a through f - the information provided by bd 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 bd.The device was not returned.
Event or Problem Description
It was reported that the patients mother said the catheter was sometimes harder to insert since the patient was older and moving more.It was unknown if the patient was able to void.

• Brand Name: MAGIC 3 PEDIATRIC CATHETER
• Common Device Name: MAGIC 3 PEDIATRIC CATHETER
• Manufacturer (Section D): C.R. BARD, INC. (COVINGTON) -1018233; 8195 industrial blvd; covington GA 30014
• MDR Report Key: 9922427
• Report Number: 1018233-2020-02337
• Device Sequence Number: 3354431
• Product Code: EZD
• UDI-Device Identifier: 00801741136863
• UDI-Public: (01)00801741136863
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K172247
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: consumer,distributor,other
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 04/28/2020

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 Model Number: 52808G
• Device Catalogue Number: 52808G
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 03/13/2020
• Supplement Date Received by Manufacturer: 04/23/2020
• Initial Report FDA Received Date: 04/03/2020
• Supplement Report FDA Received Date: 04/28/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1