MAUDE Adverse Event Report: TELEFLEX MEDICAL RUSCH MRI HANDLE BATTERIES PACK OF 1; LARYNGOSCOPE, RIGID

Model Number	IPN048614
Medical Device Problem Code	Battery Problem: Low Impedance (2973)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/22/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).
Event or Problem Description
It was reported that "power on both batteries were too low, does not light up sufficiently.There may be a loose contact".No patient involvement reported.
Event or Problem Description
It was reported that "power on both batteries were too low, does not light up sufficiently.There may be a loose contact".No patient involvement reported.
Additional Manufacturer Narrative
Qn# (b)(4).Complaint verification testing could not be performed as it was reported that the sample is not available for return.A device history record review was performed and no relevant findings were identified.Without the device to evaluate the complaint could not be confirmed and the probable cause could not be determined from the available information.Teleflex will continue to monitor and trend for reports of this nature.

• Brand Name: RUSCH MRI HANDLE BATTERIES PACK OF 1
• Common Device Name: LARYNGOSCOPE, RIGID
• Manufacturer (Section D): TELEFLEX MEDICAL; athlone
• MDR Report Key: 12168721
• Report Number: 8030121-2021-00024
• Device Sequence Number: 4199294
• Product Code: CCW
• UDI-Device Identifier: 14026704616272
• UDI-Public: 14026704616272
• Combination Product (Y/N): N
• Initial Reporter Country: AU
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,user f
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 06/22/2021

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: No Information
• Device Model Number: IPN048614
• Device Catalogue Number: 005853300
• Device Lot Number: 200201
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 06/22/2021
• Supplement Date Received by Manufacturer: 07/21/2021
• Initial Report FDA Received Date: 07/14/2021
• Supplement Report FDA Received Date: 07/21/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1