FDAFDA · Food and drugs·Recall number Z-1289-2016
Rebound Cartilage Product Usage: Rebound Cartilage is an external knee brace that provides support for knee instability due to ligament injuries and osteoarthritis.
Published April 6, 2016 · Recall initiated: February 24, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve Gray, NecLoc Extrication Collar, Rebound Cartilage, Rebound Cartilage Custom, Rebound Air Walker, Rebound Diabetic Walker, Back Support Suspenders Clip on Black, Back Support Suspenders Sew On Black, Extreme Custom, Unloader Custom XT, Unloader Custom Lite, Unloader Custom, and Papoose Infant Spine Immobilizers because the p
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Ossur H / F
- Distributor
- U.S. distribution to the following; AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, RI, TN, TX, UT, VA, VT, WA, WI, WV
- Lot
- Item No: B-254510002 B-254510003 B-254510004 B-254510005 B-254520002 B-254520003 B-254520004 B-254520005 B-254610002 B-254610003 B-254610004 B-254610005 B-254620002 B-254620003 B-254620004 B-254620005 B-254710002 B-254710003 B-254710004 B-254710005 B-254720002 B-254720003 B-254720004 B-254720005 B-254810002 B-254810003 B-254810004 B-254810005 B-254820002 B-254820003 B-254820004 B-254820005
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Iceland
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