Reported Dec 21, 2022 · Terminated

Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c)…

ARROW INTERNATIONAL Inc.

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

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: ARROW INTERNATIONAL Inc. · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437

Is this the product you have?

8 of 8 products

Products covered by this recall
#Product as published
1ASK-42703-NS
2ASK-42703-PCCH2
3ASK-42703-PUPM1
4ASK-45703-NS
5ASK-45703-PAU
6ASK-45703-PCAM1
7ASK-45703-PCCH2
8ASK-45703-PN; catheter introducer
Lot codes and dates

8 of 8 products

Products covered by this recall
#BarcodesProduct as published
110801902141030Lot Numbers: 13F22B0495 b) ASK-42703-PCCH2: UDI/DI 10801902141030
210801902159592Lot Numbers: 13F22C0862 c) ASK-42703-PUPM1: UDI/DI 10801902159592
310801902162912Lot Numbers: 13F22B0021 d) ASK-45703-NS: UDI/DI 10801902162912
410801902159110Lot Numbers: 13F22C0244 e) ASK-45703-PAU: UDI/DI 10801902159110
510801902203158Lot Numbers: 13F22D0121 f) ASK-45703-PCAM1: UDI/DI 10801902203158
610801902141047Lot Numbers: 13F22C0553 g) ASK-45703-PCCH2: UDI/DI 10801902141047
710801902140675Lot Numbers: 13F22B0641 h) ASK-45703-PN: UDI/DI 10801902140675
8Lot Numbers: 13F22C0350
Amount recalled
1275 units

This recall covers 33 products

The agency filed one notice per product. You are reading one of them; the other 32 are below.

20 more are in the archive.

Where it was sold

Why it was recalled

Stop using this product now

There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new ARROW INTERNATIONAL Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 7, 2024 · Data as of Sep 19, 5:34 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.