The Recall Desk
SevereFDA (Devices)·Z-2396-2026·Announced 2026-06-24

Arrow single lumen CVC kits contain drugs from recalled supplier

Arrow central venous catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 35,540 units are affected.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: FDA Class I recall, which the rubric floors at Severe; no death is reported in the source, so it does not escalate to Critical.

Plain-English summary

Arrow International is recalling central venous catheter kits, covering REF AK-04210 (16 GA x 8 in), AK-04300 (single lumen 16 GA x 8 in / 20 cm) and CK-04711 (14 GA x 6 in). The action covers 35,540 units.

Lidocaine, bupivacaine and 0.9% sodium chloride, the subject of a supplier recall, were included in the kits and sets. According to the manufacturer, the supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries. The FDA classified the action as Class I, its most serious classification.

Distribution was nationwide in the United States across a large number of states. The kits are supplied to healthcare facilities rather than sold to consumers.

Facilities should identify affected stock using the REF numbers, UDI-DI codes and lot numbers in the recall notice, quarantine it, and follow the instructions issued by Arrow International.

The recalled product

Product
Description/REF: CVC KIT: 16 GA X 8IN/AK-04210, CVC KIT: 1-L 16 GA X 8IN (20 CM)/AK-04300, CVC KIT: 14 GA X 6 IN/CK-04711
Manufacturer
ARROW INTERNATIONAL, LLC
Category
Medical Device — Central venous catheter kit
Hazard
Affected units
35,540

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • REF(Material)/UDI-DI/Lot(Batch): AK-04210/10801902121582
  • 10801902193275/33F24A1009
  • 33F24B0106
  • 33F24C0009
  • 33F24D0014
  • 33F24G0324
  • 33F24J0490
  • 33F24K0089
  • 33F24L0671
  • 33F25A0456
  • 33F25C0899
  • 33F25E0037
  • 33F25H0011
  • 33F25J0461
  • AK-04300/10801902121636
  • 10801902193275/33F24A1257
  • 33F24B0435
  • 33F24C0734
  • 33F24E0704
  • 33F24F0011

Distribution

Distributed nationwide across the United States.

The notice also names 52 states specifically:

Part of a larger recall action

This product is one of 35 recalled by ARROW INTERNATIONAL, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 35 products in this recall →

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Same manufacturer · ARROW INTERNATIONAL, LLC

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