HARH36 HARH36RR

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-02-04 for HARH36 HARH36RR manufactured by Stryker Sustainability Solutions Lakeland.

Event Text Entries

[182706046] The device was returned to stryker sustainability solutions for evaluation. Visual inspection revealed evidence of clinical use. The distal end of the blade was fractured and separated from the rest of the device. The device showed signs of erosion/gouges in the blade coating. A review of the dhr supports that the device met all inspection and test criteria prior to release from stryker. Therefore, the most likely root causes are: jaws/blade subassembly damage incidental and prolonged activation against solid surfaces, such as bone or plastic the instructions for use (ifu) state: use the torque wrench (already mounted to the shaft) to tighten the blade onto the hand piece. Turn the torque wrench clockwise while holding only the gray hand piece until it clicks twice indicating that sufficient torque has been applied to secure the blade. Do not attempt to bend, sharpen, or otherwise alter the shape of the blade. Doing so may cause blade failure and user or patient injury. Avoid contact with any and all other instruments while the instrument is activated. Contact with staples, clips or other instruments while the instrument is activated may result in cracked or broken blades. Note: do not use any other means than the torque wrench to attach or detach the instrument from the hand piece. Note: do not torque the instrument by hand without the torque wrench or damage may occur to the hand piece. The reported event will continue to be monitored through post-market surveillance.
Patient Sequence No: 1, Text Type: N, H10


[182706047] It was reported the blade of the harmonic scalpel tip broke off into the patient. The x-ray machine was brought in to ensure all metal was removed. The piece was retrieved completely from the patient through the same incision. There was no patient injury and extended procedure time reported was minimal at 20-30 minutes. These are commonly used devices that are readily available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001056128-2020-00007
MDR Report Key9665020
Report SourceHEALTH PROFESSIONAL
Date Received2020-02-04
Date of Report2020-02-04
Date of Event2020-01-07
Date Mfgr Received2020-01-08
Device Manufacturer Date2019-07-26
Date Added to Maude2020-02-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. MARISSA RICHMOND
Manufacturer Street1810 W. DRAKE DRIVE
Manufacturer CityTEMPE AZ 85283
Manufacturer CountryUS
Manufacturer Postal85283
Manufacturer Phone8888883433
Manufacturer G1STRYKER SUSTAINABILITY SOLUTIONS LAKELAND
Manufacturer Street5300 REGION CT
Manufacturer CityLAKELAND FL 33815
Manufacturer CountryUS
Manufacturer Postal Code33815
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNA
Generic NameSCALPEL, ULTRASONIC, REPROCESSED
Product CodeNLQ
Date Received2020-02-04
Returned To Mfg2020-01-22
Model NumberHARH36
Catalog NumberHARH36RR
Lot Number10644261
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER SUSTAINABILITY SOLUTIONS LAKELAND
Manufacturer Address5300 REGION CT LAKELAND FL 33815 US 33815


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-02-04

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