FDA Class II · Medical device · April 29, 2026
ARROW recall — ARROW INTERNATIONAL, LLC
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Official ID Z-1914-2026 · Official record ↗
⚠ Recall found. ARROW is named in 1 official recall in our current data. Details and the official notices are below — act on the remedy in the official notice.
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Official ID Z-1914-2026 · Official record ↗
See all ARROW INTERNATIONAL recalls →
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Compiled from official public-domain CPSC, NHTSA, and FDA data. Sources last checked July 24, 2026 at 3:00 AM UTC.