Orthalign, Inc 2026-04-01 Health serious FDA
Health · FDA · Recall #FDA-Z-1630-2026
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern… Recall
Issued April 1, 2026 · Orthalign, Inc
In April 2026, Orthalign, Inc recalled the Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)
What you should do
- 1 Stop using Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Orthalign, Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Orthalign, Inc
- Category
- Health
- Recall date
- April 1, 2026
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the state of UT.
- Recall number
- FDA-Z-1630-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Orthalign, Inc has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.