MAUDE Adverse Event Report: US ENDOSCOPY ETRAP; ETRAP POLYP TRAP

Model Number	00711099
Medical Device Problem Code	Suction Problem (2170)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/20/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Steris has requested the etrap-polyp trap be returned for evaluation.Investigation of this event is currently in process.A follow-up report will be submitted when additional information becomes available.
Event or Problem Description
The user facility reported that polyps were lost in their etrap-polyp trap subsequently resulting in a procedure delay.No report of injury.
Additional Manufacturer Narrative
The unit subject of the reported event was returned for evaluation.Evaluation determined there to be a slight deformation with the bridge inside the molded vessel, such that it was slanted in a slightly downward position which caused a small gap between the tray and vessel.This gap was wide enough that small polyps were able to be suctioned over the top of the tray during the retrieval process.The bridge is designed to be slanted slightly upwards during the manufacturing process to ensure there is no gap between the tray and vessel.To date, steris has received a total of eight complaints reporting that polyps were not retained within the etrap.The complaints were received across four different lots (the other three lots were unknown as the product was discarded), manufactured between december 2023 - august 2024.The four known lots were manufactured using the same mold tool.Additional investigation of the mold tool used to produce the vessels determined that water used to cool the molds during the production process may have been inconsistently delivered due to an issue with the water line.This may have resulted in excess heat to a small number of vessels, resulting in the observed deformation.This mold tool was replaced in august 2024.An analysis of all product manufactured on this mold tool for this 9-month period determined there were a total of (b)(4) etraps manufactured across (b)(4) lots.This results in a reported failure rate of approximately (b)(4), further evidencing the extremely intermittent nature of the issue.The etrap is also a historically high turnover product i.E., customers order and use the product quickly.As of january 2025, nearly all of the customers who had ordered product during the 9-month time period have already reordered newer product (after august 2024); therefore, it is reasonable to assume that most or all of the product from this time period has already been used.This is further supported based on the fact that the most recent complaint for this issue was received in august 2024.Based on the overall analysis, and corrective actions already taken, further action is not planned at this time.Steris will continue to monitor under our post-market surveillance procedures to ensure the product continues to perform as intended.Udi related data clarification - the lot/serial number is unknown, therefore, the applicable production identifiers were not included in the mdr.

• Brand Name: ETRAP
• Common Device Name: ETRAP POLYP TRAP
• Manufacturer (Section D): US ENDOSCOPY; 5976 heisley road; mentor OH 44060
• Manufacturer (Section G): US ENDOSCOPY; 5976 heisley road; mentor OH 44060
• Manufacturer Contact: coletta cohara ; 5976 heisley road; mentor, OH 44060 ; 4404130648
• MDR Report Key: 20263224
• Report Number: 1528319-2024-00076
• Device Sequence Number: 8261230
• Product Code: KDQ
• UDI-Device Identifier: 00724995184728
• UDI-Public: (01)00724995184728
• Combination Product (Y/N): N
• Initial Reporter State: WI
• Initial Reporter Country: US
• 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 Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 09/19/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 00711099
• Device Catalogue Number: 00711099
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/20/2024
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 09/19/2024
• Supplement Report FDA Received Date: 01/28/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• 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