FreshRecalls

Description/REF: recall status

⚠ Recall found. Description/REF is named in 34 official recalls in our current data. Details and the official notices are below — act on the remedy in the official notice.

Brand
ARROW INTERNATIONAL

Recalls naming this model

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

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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-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-2397-2026 · Official record ↗

See all ARROW INTERNATIONAL recalls →

Verify with the official sources:

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Compiled from official public-domain CPSC, NHTSA, and FDA data. Sources last checked July 24, 2026 at 1:09 AM UTC.