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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STAXI CORPORATION STAXI MEDICAL CHAIR; CHAIR, ADJUSTABLE, MECHANICAL
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STAXI CORPORATION STAXI MEDICAL CHAIR; CHAIR, ADJUSTABLE, MECHANICAL Back to Search Results
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Type  malfunction  
Event Description
Stryker medical was notified of a potentially reportable complaint involving a product for which stryker is not the original equipment manufacturer of the reported device.The customer alleged a manufacturer staxi chair, serial number (b)(6) that had a footrest that would not support weight.This report reflects information received by fda in the form of a notification per 803.22 (b)(2).
 
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Brand Name
STAXI MEDICAL CHAIR
Type of Device
CHAIR, ADJUSTABLE, MECHANICAL
Manufacturer (Section D)
STAXI CORPORATION
MDR Report Key18193041
MDR Text Key329064675
Report NumberMW5148388
Device Sequence Number1
Product Code INN
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Unknown
Type of Report Initial
Report Date 11/19/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received11/21/2023
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Patient Sequence Number1
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