FreshRecalls

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

ARROW (1)ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code (1)Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code (1)Arrow Edge Hemodialysis Catheterization Product (1)Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter (1)Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7 (1)Cannon II Plus Hemodialysis Catheter (1)Description/REF (34)FLEXTIP PLUS EPIDURAL CATHETER (1)MAC" Two-Lumen Central Venous Access Kit for use with 7 (1)NextStep Antegrade Chronic Hemodialysis Catheter (1)PARACENTESIS KIT (1)PERCUTANEOUS SHEATH INTRODUCER with 7 (1)Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code (1)

All ARROW INTERNATIONAL recalls

FDA Class I · Medical device · June 24, 2026

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

Description/REF recall — ARROW INTERNATIONAL, LLC

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

PARACENTESIS KIT recall — ARROW INTERNATIONAL, LLC

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

NextStep Antegrade Chronic Hemodialysis Catheter recall — ARROW INTERNATIONAL, LLC

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

Cannon II Plus Hemodialysis Catheter recall — ARROW INTERNATIONAL, LLC

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

Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter recall — ARROW INTERNATIONAL, LLC

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

Arrow Edge Hemodialysis Catheterization Product recall — ARROW INTERNATIONAL, LLC

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

Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7 recall — ARROW INTERNATIONAL, LLC

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

MAC" Two-Lumen Central Venous Access Kit for use with 7 recall — ARROW INTERNATIONAL, LLC

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

Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code recall — ARROW INTERNATIONAL, LLC

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

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 ↗

FDA Class II · Medical device · April 29, 2026

FLEXTIP PLUS EPIDURAL CATHETER recall — ARROW INTERNATIONAL, LLC

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

PERCUTANEOUS SHEATH INTRODUCER with 7 recall — ARROW INTERNATIONAL, LLC

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

ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code recall — ARROW INTERNATIONAL, LLC

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

Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code recall — ARROW INTERNATIONAL, LLC

Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured

Official ID Z-1910-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked July 24, 2026 at 1:09 AM UTC.