Reported Apr 9, 2025 · Ongoing
Monterey AL Implant Inserter; 18/20mm; Catalog 48019130.
Stryker Spine
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Stryker Spine · 59 State Rt 17 S · Allendale, NJ · 07401-1614
Is this the product you have?
Monterey AL Implant Inserter18/20mmCatalog 48019130
- Lot codes and dates
- Catalog 48019130
- UDI-DI07613327501049
- Lot Number231639
- Amount recalled
- 46 units (44 US, 2 OUS)
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
Potential for the gold unlock button to separate from the inserter.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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