MAUDE Adverse Event Report: RAYNHAM CODMAN SURG STRP1/2X6-200; SURGICAL STRIPS

Model Number	801451
Medical Device Problem Code	Component Missing (2306)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/10/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
An investigation has been initiated based on the reported information.Upon completion of the investigation, a follow-up report will be submitted.
Event or Problem Description
A facility reported an incorrect number of pads in a surgical strips package (id 801451).Only 9 out of 10 pads were found in the package.The issue was discovered after the surgery during the final count.A 45-minute delay was noted looking for the patty and no patient injury reported.
Event or Problem Description
N/a.
Additional Manufacturer Narrative
The surgical strips (id (b)(4) was not returned for evaluation as the product is not available for return as per customer; therefore, an evaluation of the device could not be performed.Lot number information has been provided; therefore, device history record (dhr) was reviewed, and no anomalies were found.The root cause(s) of the reported issue could not be determined.If additional relevant information becomes available in the future, this complaint will be reopened, and the respective evaluation performed.Trends will be monitored for this and similar issues.At present, we consider this complaint to be closed.There is currently an open corrective and preventative action for the patties/strips product family related to x-ray polymer issues, string issues and incorrect count.

• Brand Name: CODMAN SURG STRP1/2X6-200
• Common Device Name: SURGICAL STRIPS
• Manufacturer (Section D): RAYNHAM; 325 paramount drive; 325 paramount drive; raynham MA
• Manufacturer (Section G): RAYNHAM; 325 paramount drive; raynham MA
• Manufacturer Contact: vivian nelson ; 1100 campus drive; princeton, NJ ; 6099362319
• MDR Report Key: 17042736
• Report Number: 3014334038-2023-00080
• Device Sequence Number: 8739122
• Product Code: HBA
• UDI-Device Identifier: 10381780515074
• UDI-Public: 10381780515074
• Combination Product (Y/N): N
• PMA/510(K) Number: K880402
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 07/20/2023

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: 801451
• Device Catalogue Number: 801451
• Device Lot Number: 6788681
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 05/15/2023
• Supplement Date Received by Manufacturer: 07/13/2023
• Initial Report FDA Received Date: 06/01/2023
• Supplement Report FDA Received Date: 07/20/2023
• Date Device Manufactured: 11/10/2022
• 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: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown