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FDA Medical Device Recalls (openFDA)

Smith & Nephew, Inc.: LEGION Posterior Stabilized OXINIUM Femoral Component, REF 71421216, Size 6, Left, Nonporous Femoral Component, A/P 65.5 MM, M/L 73 MM, For Cemented Use Only, ZR-2.5NB,Sterile. Knee prosthesis component.

Recall number
Z-1951-2021
Recalling firm
Smith & Nephew, Inc.
Product
LEGION Posterior Stabilized OXINIUM Femoral Component, REF 71421216, Size 6, Left, Nonporous Femoral Component, A/P 65.5 MM, M/L 73 MM, For Cemented Use Only, ZR-2.5NB,Sterile. Knee prosthesis component.
Status
Terminated
Initiated
2021-05-19
Posted
not on file
Terminated
2023-04-14
Reason
The device components experienced a manufacturing process error that resulted in surface damage from product handling.
Root cause
Nonconforming Material/Component
Action
On 5/19/2021, the firm issued letters dated 5/19/2021 via overnight mail or via email explaining the issue, potential risk of use of the product, and required actions, which are listed on the response form.
Quantity
5 units
Distribution
US Nationwide distribution in the states of FL, NE, NY, and TX. There was no foreign/government/military distribution.
Lot, serial or model codes
Lot 20HM17607
510(k) numbers
["K043440"]
PMA numbers
not on file
Product code
JWH
Firm FEI
1020279
Firm city
Memphis
Firm state
TN
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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