Recall archive

94,355 stored notices, from Jun 20, 2012 to Sep 23, 2026.

3 recalls · page 1 of 1

Reported Jun 24, 2026

PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Arrow International, LLC

Matched: Brand — 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…

34 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2026

Arrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS-15322-I

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Arrow International, LLC

Matched: Brand · Product · Product details — 16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer…

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2026

Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arrow International, LLC

Matched: Brand · Product · Product details — Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured

7 more products in this recall

FDA (openFDA device enforcement)

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