Skip to content
Recall Observatory FDA recall evidence

Device product

smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT, SIZE 5N, LEFT, NARROW, REF 71421265; knee joint

Z-2621-2023

August 31, 2023

Class II

Product summary

Firm
Smith & Nephew Inc
Event
Event 92976
Status
Ongoing
Classification
Class II
Quantity
8 units
Official record key
device-enforcement:Z-2621-2023

Official wording

Reason: The firm conducting a recall due to a complaint received indicating that a package contained a LEGION NARROW PS OXIN SZ 4N LT implant instead of a LEGION NARROW PSvOXIN SZ 5N LT as described on the product label.

Code information: UDI/DI: 00885556234006, Lot Number: 23EM09878

Distribution pattern: OH, CT, TX, NC, CA, NE, NV

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The firm conducting a recall due to a complaint received indicating that a package contained a LEGION NARROW PS OXIN SZ 4N LT implant instead of a LEGION NARROW PSvOXIN SZ 5N LT as described on the product label.