Pdg Product Design Group Inc: Medical Device Recall in 2014 - (Recall #: Z-2695-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 12, 2012

Date Posted: October 1, 2014

Recall Number: Z-2695-2014

Event ID: 69035

Reason for Recall:

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.

Status: Terminated

Product Quantity: 153

Code Information:

Fuze T50, Fuze T20 and Fuze T50 Jr 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 52825 52699 52698 52672 52684 52708 52737 52771 52803 52858 52870 52883 52829 52706 52834 52668 52685 52710 52738 52772 52805 52859 52871 52884 52916 52751 52821 52673 52687 52709 52739 52773 52806 52860 52872 52885 52767 52799 53192 52674 52690 52711 52740 52774 52807 52861 52873 52886 52795 52914 52663 52676 52688 52726 52741 52775 52808 52862 52874 52887 52919 52824 52664 52677 52691 52728 52742 52776 52809 52863 52876 52888 52831 52918 52665 52675 52693 52727 52743 52777 52810 52864 52877 52889 52754 52917 52733 52678 52694 52730 52744 52778 52811

Distribution Pattern:

Worldwide Distribution- US Distribution including the states of : AZ, CA, GA, KY, MI, MN, MO, MS, NC, NE, NY, OH, PA, SC, TX, VA, and WA., and Internationally to Canada and Hong Kong.

Voluntary or Mandated:

Voluntary: Firm initiated