MAUDE Adverse Event Report: STRYKER ENDOSCOPY-SAN JOSE ALPHAVENT SUTURE ANCHOR 4.75MM PEEK SUTURE ANCHOR WITH 3 STRANDS 1.4MM X; FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE

Catalog Number	3910-947-131
Medical Device Problem Code	Device Contaminated During Manufacture or Shipping (2969)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	09/26/2025
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that there looks to be some loose fuzz/plastic in the packaging.
Additional Manufacturer Narrative
Additional information will be provided once the investigation has been completed.
Additional Manufacturer Narrative
The device was not returned for investigation.This complaint investigation was closed based on the device not received, therefore the reported failure mode was not confirmed.In the event that the device is received, the complaint will be reopened and the investigation will be updated with new results.Alleged failure: foreign material found inside the sterile packaging.Probable root cause: process.Uncontrolled environmental conditions.The reported failure mode will be monitored for future reoccurrence.
Event or Problem Description
It was reported that there looks to be some loose fuzz/plastic in the packaging.

• Brand Name: ALPHAVENT SUTURE ANCHOR 4.75MM PEEK SUTURE ANCHOR WITH 3 STRANDS 1.4MM X
• Common Device Name: FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE
• Manufacturer (Section D): STRYKER ENDOSCOPY-SAN JOSE; 5900 optical court; san jose CA 95138
• Manufacturer (Section G): STRYKER ENDOSCOPY-SAN JOSE; 5900 optical court; san jose CA 95138
• Manufacturer Contact: arsalan rizvi ; 5900 optical court; san jose, CA 95138 ; 4087542000
• MDR Report Key: 23381514
• Report Number: 0002936485-2025-00885
• Device Sequence Number: 4940445
• Product Code: MBI
• UDI-Device Identifier: 07613327563115
• UDI-Public: 07613327563115
• Combination Product (Y/N): N
• Initial Reporter State: MO
• Initial Reporter Country: US
• PMA/510(K) Number: K211502
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 01/08/2026

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 Catalogue Number: 3910-947-131
• Device Lot Number: 24232AE2
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 09/26/2025
• Supplement Date Received by Manufacturer: 12/26/2025
• Initial Report FDA Received Date: 10/24/2025
• Supplement Report FDA Received Date: 01/08/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 08/19/2024
• 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
• Patient Sex: Unknown