Rebound Air Walker Product Usage: Rebound Air Walkers recall
Rebound Air Walker Product Usage: Rebound Air Walkers are indicated for grade 2 and grade 3 ankle sprains, to stabilize fractures, post-operative use…
Why was Rebound Air Walker Product Usage: Rebound Air Walkers recalled?
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 should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Item No: B-242900001 B-242900001E B-242900001SE B-242900002 B-242900002E B-242900002SE B-242900003 B-242900003E B-242900003SE B-242900004 B-242900004E B-242900004SE B-242900005 B-242900005E B-242900005SE B-242900061 B-242900061E B-242900061SE B-242900062 B-242900062E B-242900062SE B-242900063 B-242900063E B-242900063SE B-242900064 B-242900064E B-242900064SE B-242900065 B-242900065E B-242900065SE
- Product
- Rebound Air Walker Product Usage: Rebound Air Walkers are indicated for grade 2 and grade 3 ankle sprains, to stabilize fractures, post-operative use…
- Recalling firm
- Ossur H / F
- Quantity
- 7623
- Distribution
- 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
- Recall date
- April 6, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)