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Serious recall: Injury is possible or has been reported. Take action promptly.

Stryker Spine 2025-04-09 Health serious FDA
Health · FDA · Recall #FDA-Z-1489-2025

Monterey AL Implant Inserter; 14/16mm; Catalog 48019120. Recall

Issued April 9, 2025 · Stryker Spine

In April 2025, Stryker Spine recalled the Monterey AL Implant Inserter; 14/16mm; Catalog 48019120., a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Potential for the gold unlock button to separate from the inserter.

What you should do

  1. 1 Stop using Monterey AL Implant Inserter; 14/16mm; Catalog 48019120. right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Stryker Spine to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Stryker Spine
Category
Health
Recall date
April 9, 2025
Units affected
Not reported
Sold at
Domestic: CA, CO, FL, GA, IL, MA, NE, NH, NY, OK, PA, TX, UT. International: Canada.
Recall number
FDA-Z-1489-2025
Made in
United States
Issuing agency
FDA

In context

  • Stryker Spine has 1 recall in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 691st Health recall we've logged in 2025.
Read the official FDA notice

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