Reported Oct 1, 2014 · Terminated

Fuze Manual Tilt Wheelchair. Fuze T50, Fuze T20 and Fuze T50 Jr

Pdg Product Design Group Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Pdg Product Design Group Inc · 9165 Shaughnessy St · Vancouver, British Columbia · N/A

Is this the product you have?

    • Fuze Manual Tilt Wheelchair. Fuze T50
    • Fuze T20 and Fuze T50 Jr
Lot codes and dates
  • Fuze T50, Fuze T20 and Fuze T50 Jr

    153 of 153 codes

    • 52752
    • 52794
    • 52750
    • 52667
    • 52679
    • 52692
    • 52729
    • 52745
    • 52779
    • 52826
    • 52865
    • 52878
    • 52823
    • 52912
    • 52804
    • 52666
    • 52680
    • 52702
    • 52731
    • 52746
    • 52780
    • 52827
    • 52866
    • 52879
    • 52749
    • 52913
    • 52753
    • 52669
    • 52682
    • 52703
    • 52732
    • 52747
    • 52781
    • 52828
    • 52867
    • 52880
    • 52696
    • 52796
    • 52734
    • 52670
    • 52681
    • 52695
    • 52735
    • 52768
    • 52782
    • 52856
    • 52868
    • 52881
    • 52748
    • 52705
    • 52701
    • 52671
    • 52683
    • 52707
    • 52736
    • 52770
    • 52802
    • 52857
    • 52869
    • 52882
Amount recalled
153

Where it was sold

Why it was recalled

The hex bolt head might shear and cause the axle plate to detach from the lower frame of the wheelchair and could collapse the wheels while in use.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 23, 2015 · Data as of Sep 19, 5:28 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.