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All product recalls associated with Konica Minolta Healthcare Americas, Inc..
Total Recalls
8
Past Year
0
Class I (Serious)
0
Most Recent
Dec 2021
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel potential risk of incorrect length measurement/area calculation if incorrect power sequence is followed
Koni North America (KONI) is recalling certain shock absorbers with model numbers 8245-1146L, 8245-1146R, 8245-1201L, 8245-1201R, 8245-1203L, and 8245-1203R. These shock absorbers were manufactured January 2008 through April 2013. The affected absorbers were manufactured with an incorrectly welded bracket which may cause the shock absorber to bend and rest on the drive shaft.
KONI NORTH AMERICA (KONI) IS RECALLING CERTAIN AFTERMARKET, 30-SERIES, SHOCK ABSORBERS; PART NUMBERS 30-1720 AND 30-1721. THE EYE LOOP WELD TO THE EYE BASE DID NOT HAVE ENOUGH WELD PENETRATION AND COULD RESULT IN A FAILED WELD.