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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SUNRISE MEDICAL (US) LLC QUICKIE QM710; POWERED WHEELCHAIR

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SUNRISE MEDICAL (US) LLC QUICKIE QM710; POWERED WHEELCHAIR Back to Search Results
Model Number QM710
Medical Device Problem Code Unstable (1667)
Health Effect - Clinical Code Laceration(s) (1946)
Date of Event 09/07/2017
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
Background information: the suspa suspension spring is used to allow the user to navigate variable terrain while maintaining steering and drive control and consists of a cylinder with an internal fluid-pressure system.The suspa spring experiences loss of pressure by failure of one or more internal seals that control pressurized fluid (leak) or through the failure of the spring pin in the locked position.The loss of pressure results in the user experiencing deterioration in stability, raising of the front casters, forward pitching of the chair and/or veering to the side when decelerating which are known issues addressed in the risk management file.If these were to occur the user may be thrown from the chair which could cause injury or impairment requiring immediate, invasive professional medical intervention.The positioning belt is a current control set in place to support the end user's posture and to limit slipping and/or sliding and a performance spring is incorporated as a design control to reduce the severity of occurrence by adding additional pressure to stabilize the front caster arms.Redesign of the suspension spring to allow for higher curb climbing capability was launched in (b)(6).Discussion: it is likely that the suspa suspension spring issue led to the user's complaint whereby he fell from the chair.While cuts and scrapes are not considered a serious injury, due to the malfunction and the chair tipping over, it is likely that this malfunction, should it recur, could result in a serious injury.Therefore, this incident meets the requirements for a reportable event.Conclusion: the suspa spring issue is a known issue that has been remediated internally.While the risk ranking is fairly low, it could potentially result in a serious injury and, therefore, is a reportable event.This incident is being reported as a malfunction with potential serious injury through the fda's medwatch program.Additional information: this complaint has been re-reviewed as a part of a four-year retrospective review and remediation effort based on enhancements made to the company's complaint handling and adverse event reporting processes.A legal consulting firm was consulted for the retrospective review.This mdr is being filed based on the outcome of that retrospective review.
 
Event or Problem Description
End user reported that he was walking the dog and as he turned around the shocks failed causing the chair to tip onto its side.He reports that he suffered cuts and scrapes on his shoulder, leg, arms and back.
 
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Brand Name
QUICKIE QM710
Common Device Name
POWERED WHEELCHAIR
Manufacturer (Section D)
SUNRISE MEDICAL (US) LLC
2842 n business park ave
fresno CA 93702 1328
MDR Report Key12304487
Report Number2937137-2021-00035
Device Sequence Number3971209
Product Code ITI
UDI-Device Identifier00016958052367
UDI-Public(01)00016958052367
Combination Product (Y/N)N
Initial Reporter CountryUS
PMA/510(K) Number
K060531
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)Unknown
Reporter Type Manufacturer
Report Source consumer
Initial Reporter Occupation Other
Type of Report Initial
Report Date (Section B) 08/10/2021
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 Lay User/Patient
Device Model NumberQM710
Device Catalogue NumberEIPW11
Type of Report(Section G)Initial
Initial Date Received by Manufacturer 09/07/2017
Initial Report FDA Received Date08/10/2021
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
Outcome Attributed to Adverse Event Other;
Patient Age65 YR
Patient Weight95
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