MAUDE Adverse Event Report: CARDINAL HEALTH SALEM SUMP W/ ARV 18FR. 48IN; TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION

Model Number	8888266148
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Perforation of Esophagus (2399)
Date of Event	06/08/2023
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
An investigation is currently underway.Upon completion, the results will be forwarded.
Event or Problem Description
The customer reported that while the item was being inserted into the patient's esophagus, a perforation occurred causing injury to the patient.The customer stated that they cannot be sure if the perforation was caused due to a defect on the item itself or if it was an error in executing the procedure using the product.Additional information provided on (b)(6) 2023 stated that the perforation was on the esophagus.As a result, the patient required an emergent exploration of neck repair of esophageal perforation.No additional injury or intervention was required.The patient's current status is stable.Additional information provided on (b)(6) 2023 stated that the patient originally went to the hospital for a d&c.The initial reason for the salem sump placement was due to general anesthesia.The salem sump was placed in the or by a md and crna.
Additional Manufacturer Narrative
We have concluded our investigation process related to the reported complaint.Based on the information available to us, we were unable to confirm the event.In the meantime, all information received will be used for further tracking and trending purposes.

• Brand Name: SALEM SUMP W/ ARV 18FR. 48IN
• Common Device Name: TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION
• Manufacturer (Section D): CARDINAL HEALTH; 777 west street; mansfield MA 02048
• Manufacturer (Section G): CARDINAL HEALTH; calle 9 sur no. 125 cuidad ind; tijuana 22500 ; MX 22500
• Manufacturer Contact: jill saraiva ; 777 west street; mansfield, MA 02048 ; 5086183640
• MDR Report Key: 17393963
• Report Number: 9612030-2023-03770
• Device Sequence Number: 5955699
• Product Code: FEG
• UDI-Device Identifier: 10884521004726
• UDI-Public: 10884521004726
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: User Facility,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 10/13/2023

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
• Operator of Device: Health Professional
• Device Model Number: 8888266148
• Device Catalogue Number: 8888266148
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/12/2023
• Supplement Date Received by Manufacturer: 07/12/2023
• Initial Report FDA Received Date: 07/25/2023
• Supplement Report FDA Received Date: 10/13/2023
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: A
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 49 YR
• Patient Sex: Female
• Patient Weight: 120 KG
• Patient Race: Black Or African American