ARROW INTERNATIONAL recalls
47 recent recalls on record for ARROW INTERNATIONAL in CPSC, NHTSA, and FDA data as of July 24, 2026 at 1:09 AM UTC.
Models with recalls
All ARROW INTERNATIONAL recalls
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2397-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2396-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2395-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2394-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2393-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2392-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2391-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2390-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2389-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2388-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2387-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2386-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2385-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2384-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2383-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2382-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2381-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2380-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2379-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2378-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2377-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2376-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2375-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2374-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2373-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2372-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2371-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2370-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2369-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2368-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2367-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2366-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2365-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2364-2026 ·
Official record ↗
FDA Class I · Medical device · June 24, 2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Official ID Z-2363-2026 ·
Official record ↗
FDA Class I · Medical device · May 20, 2026
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Official ID Z-2159-2026 ·
Official record ↗
FDA Class I · Medical device · May 20, 2026
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Official ID Z-2158-2026 ·
Official record ↗
FDA Class I · Medical device · May 20, 2026
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Official ID Z-2157-2026 ·
Official record ↗
FDA Class I · Medical device · May 20, 2026
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and …
Official ID Z-2156-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Official ID Z-1917-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Official ID Z-1916-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Official ID Z-1915-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Official ID Z-1914-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Official ID Z-1913-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Official ID Z-1912-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Official ID Z-1911-2026 ·
Official record ↗
FDA Class II · Medical device · April 29, 2026
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
Official ID Z-1910-2026 ·
Official record ↗
Compiled from official public-domain government data. Last checked July 24, 2026 at 1:09 AM UTC.