[Recalled] Rebound Air Walker Product Usage: Rebound Air Walkers are indicated for grade 2 and grade 3 ankle sprains, to stabilize fractures, post-operative use, and trauma or rehab use. — Ossur Americas is recalling , Knee Shield / Pat
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| 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, and trauma or rehab use. |
|---|---|
| Brand / manufacturer | Ossur H / F |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1291-2016 |
| Country of notice | Iceland |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 24 February 2016 |
| EAN / barcode | 242900001 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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
This Class II recall concerns device products distributed in Iceland and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Ossur H / F
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.