MAUDE Adverse Event Report: DAVIS & GECK CARIBE LTD MAXON; SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID

Model Number	8886623351
Medical Device Problem Codes	Detachment of Device or Device Component (2907); Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	Insufficient Information (4580)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
D10 concomitant products: 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y); 8886623351, 8886 6233-51 maxon 2-0 grn 75cm v20x36 (lot#d3h1779y) medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.
Event or Problem Description
According to the reporter, the sutures were breaking off at the needle.This issue occurred on 15 devices.
Additional Manufacturer Narrative
Additional information received shows that there is no information to reasonably suggest that the device in this report may have caused or contributed to a death or serious injury or that the device in this report has malfunctioned.Therefore, this event does not meet the reporting requirements in 21 cfr 803.Medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.
Event or Problem Description
According to the reporter, during a veterinary procedure, prior to the patient's use, after opening the packaging, the sutures were breaking off at the needle base (swedge).This issue occurred on four devices.To resolve the issue, another package of suture was used.There was no patient injury.

• Brand Name: MAXON
• Common Device Name: SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID
• Manufacturer (Section D): DAVIS & GECK CARIBE LTD; zona franca de san isidro; santo domingo 0101 ; DR 0101
• Manufacturer (Section G): DAVIS & GECK CARIBE LTD; zona franca de san isidro; santo domingo 0101 ; DR 0101
• Manufacturer Contact: justin ellis ; 8200 coral sea st ne; mounds view, MN 55112 ; 7635265677
• MDR Report Key: 21404906
• Report Number: 9612501-2025-00454
• Device Sequence Number: 20912279
• Product Code: GAM
• UDI-Device Identifier: 10884523002430
• UDI-Public: 10884523002430
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K990951
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative,Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 02/28/2025

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: Health Professional
• Device Model Number: 8886623351
• Device Catalogue Number: 8886623351
• Device Lot Number: D3H1779Y
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/29/2025
• Supplement Date Received by Manufacturer: 02/11/2025
• Initial Report FDA Received Date: 02/18/2025
• Supplement Report FDA Received Date: 02/28/2025
• Date Device Manufactured: 08/10/2023
• 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
• Concomitant Medical Products and Therapy/Usage Dates: SEE H11
• Patient Sex: Unknown