Lower riskMedical device recall · FDA · Published June 8, 2020
New Standard Device 1.8mm Truss Wire Recall: Component for Metalogix Revolution Plating
New Standard Device recalls 1.8mm truss wire (REF: 900217) used in Metalogix Revolution External Plating System. This component is being replaced with stronger 2.0mm wires to reduce breakage.
1.8mm truss wires are being removed to facilitate the introduction of 2.0mm truss wires. The increased wire diameter and new manufacturing process are meant to provide a stronger wire and reduced breakage.
Take action
Contact the company
📍Recalling firmNew Standard Device Inc4848 Research Dr · San Antonio, TX 78240-5005
“New Standard Device 1.8mm Truss Wire Recall: Component for Metalogix Revolution Plating.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/65016-new-standard-device-1-8mm-truss-wire-recall-component-for. Based on FDA recall #Z-1236-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1236-2022%22&limit=1).
The Food and Drug Administration announced on June 8, 2020, that New Standard Device Inc is recalling 1.8mm Truss Wire (REF: 900217), a component of the Metalogix Revolution External Plating System. The recall involves 426 units distributed nationwide in Arizona, Virginia, Ohio, Connecticut, Texas, North Carolina, and Georgia.
How to tell if you have it
Brand: New Standard Device
Product: 1.8mm Truss Wire, REF: 900217
Component of: Metalogix Revolution External Plating System
UDI: 854641008419
Lots: A29518X and A17219DA
Quantity: 426 units
The hazard
The agency states that the 1.8mm truss wires are being removed to facilitate the introduction of 2.0mm truss wires. The increased wire diameter and new manufacturing process are intended to provide a stronger wire and reduced breakage.
Context
GovInfoNow's records show New Standard Device Inc has 3 other recalls on record since July 23, 2019. On Dec. 28, 2020, the company issued a recall for Metalogix Self-Drill Half-Pins due to tip breakage during surgery. An Aug. 14, 2019, recall addressed stripping nuts hazards in New Standard Device Metalogix Slotted Wrenches caused by manufacturing processing errors. A July 23, 2019, recall involved thread stripping of 'n'-Hole Posts during the application process.
How to tell if you have this one
Check for the 1.8mm truss wire with reference number 900217 in the Metalogix Revolution External Plating System. Lot numbers A29518X and A17219DA are also associated with this component.
Brand
New Standard Device
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify if your Metalogix Revolution External Plating System uses the 1.8mm truss wire (REF: 900217) with lot numbers A29518X or A17219DA.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 7 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of AZ, VA, OH, CT, TX, NC, GA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, Connecticut, Georgia, North Carolina, Ohio, Texas, Virginia.
Recall timeline
FDA published this recall 2 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
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-1236-2022 (June 8, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1236-2022 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.