Lower riskMedical device recall · FDA · Published April 19, 2022
Smith & Nephew Legions Narrow PS OXIN Recalled Due to Mislabeling
Smith & Nephew recalls two surgical products due to mislabeling in shipments. Affected items may be confused with different models, but no safety hazard is reported.
“Smith & Nephew Legions Narrow PS OXIN Recalled Due to Mislabeling.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60799-smith-nephew-legions-narrow-ps-oxin-recalled-due-to-mislabeling. Based on FDA recall #Z-1099-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1099-2022%22&limit=1).
Smith & Nephew Inc recalled LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5 devices due to mislabeling hazards, according to the FDA on April 19, 2022.
How to tell if you have it
Smith & Nephew LEGION NARROW PS OXIN SZ 6N RT, Model Number: 71421276, Lot: 21JM17389
Smith & Nephew JRNY II BCS FEMORAL OXIN LT SZ 5, Model Number: 74022125, Lot: 21JM18618
The hazard
The FDA reported that a JRNY II BCS Femoral OXIN LT SZ5 was found in a box labeled as a LEGION NARROW PS OXIN SZ 6N RT.
Context
GovInfoNow's records show Smith & Nephew, Inc. has 66 other recalls on record since July 24, 2017. Recent Smith & Nephew recalls include the TRIGEN Humeral Nail Recall on March 16, 2026, and the BIOSURE HA Screw Recall on November 24, 2025. Other recent recalls of similar products include Omnicell i.v.Station Label Stock Recall (March 25, 2026), Fresenius Medical Care Bicarby Dialysate Recall (May 7, 2026), and Medline TRACH TUBE KIT Recall (July 10, 2026).
How to tell if you have this one
Check for the model numbers: 71421276 (LEGION NARROW PS OXIN SZ 6N RT) or 74022125 (JRNY II BCS FEMORAL OXIN LT SZ 5). The products were sold with specific lot numbers and unique identifiers.
Brand
Smith & Nephew
Product
Smith & Nephew Inc recalls LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Labels
Look for the model numbers on the product: 71421276 or 74022125.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 8 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide distribution - US Nationwide distribution in the states of CT, NC, CO, SC, VA, FL, IL, CA and the country of Japan.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Colorado, Connecticut, Florida, Illinois, North Carolina, South Carolina, Virginia.
Recall timeline
FDA terminated this recall 2.3 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1099-2022 (April 19, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1099-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.