MAUDE Adverse Event Report: MEDLINE INDUSTRIES, LP; ROBOTICS

Catalog Number DYNJ909084

Device Problem Appropriate Term/Code Not Available (3191)

Patient Problem Foreign Body In Patient (2687)

Event Date 01/25/2024

Event Type  Injury  

Event Description

According to the facility on (b)(6) 2024 during a robotic ventral incisional hernia repair the "raytec sponges used intraabdominally unraveled and separated upon removal".

Manufacturer Narrative

According to the facility on (b)(6) 2024 during a robotic ventral incisional hernia repair the "raytec sponges used intraabdominally unraveled and separated upon removal".Per the facility the gauze were being unfolded during use and an additional xray was needed.Per the facility the patient was discharged, and the procedure was able to be completed.No additional information is available at this time.The sample was requested for evaluation.It has been determined that the reported event could cause or contribute to serious injury if it were to occur.In an abundance of caution, this medwatch is being filed.If any further relevant information is identified or obtained, a supplemental medwatch will be submitted.

• Type of Device: ROBOTICS
• Manufacturer (Section D): MEDLINE INDUSTRIES, LP; three lakes drive; northfield IL 60093
• Manufacturer Contact: justin herrmann ; three lakes drive; northfield, IL 60093
• MDR Report Key: 18678397
• MDR Text Key: 335030292
• Report Number: 1423395-2024-00014
• Device Sequence Number: 1
• Product Code: OHD
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 02/09/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 02/09/2024
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Catalogue Number: DYNJ909084
• Device Lot Number: 23IBU374
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 01/26/2024
• Was Device Evaluated by Manufacturer?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1
• Patient Outcome(s): Other