MAUDE Adverse Event Report: STRYKER ENDOSCOPY-SAN JOSE PROCINCH ADJUSTABLE LOOP IMPLANT, REVERSE TENSIONING; FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE

Model Number	234-102-060
Medical Device Problem Code	Expiration Date Error (2528)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/05/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Additional information will be provided, once the investigation has been completed.
Event or Problem Description
It was reported, that an expired product was used.
Event or Problem Description
It was reported that an expired product was used.
Additional Manufacturer Narrative
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: product was implanted.Probable root cause: design -validated shelf life too short -shelf life/expiration date not adequately published on package application -distribution inefficient, sat too long in inventory before being shipped to customer -user inattentive to expiration date of product the reported failure mode will be monitored for future reoccurrence.

• Brand Name: PROCINCH ADJUSTABLE LOOP IMPLANT, REVERSE TENSIONING
• 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: lucas wolski ; 5900 optical court; san jose, CA 95138 ; 4087542000
• MDR Report Key: 17076059
• Report Number: 0002936485-2023-00562
• Device Sequence Number: 6841813
• Product Code: MBI
• UDI-Device Identifier: 07613327137385
• UDI-Public: 07613327137385
• Combination Product (Y/N): N
• Initial Reporter Country: SP
• PMA/510(K) Number: K150416
• 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): 04/12/2024

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: 234-102-060
• Device Catalogue Number: 234-102-060
• Device Lot Number: 20349AE2
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 05/10/2023
• Supplement Date Received by Manufacturer: 05/10/2023
• Initial Report FDA Received Date: 06/06/2023
• Supplement Report FDA Received Date: 04/12/2024
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 12/14/2020
• 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