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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Arrow International Inc: These finished good kits may contain the incorrect Springwire Guide (SWG).

Agency Publication Date: February 20, 2018
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Affected Products

Product: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product Code: ASK 42703 PUHC; Exp. Dates Feb 2018 - Nov 2018

Lot number: 23F16M0054

Lot Numbers:
number
Product: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter and Sharps Safety Features; Product Code: ASK 15703 NYP; Exp. Dates Feb 2018 - Nov 2018

Lot number: 13F16M0196

Lot Numbers:
number
Product: Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous Catheterization Kit; Product Codes: ASK-45703-PNHS; ASK-45703-PGMCL; ASK-45703-PNW; Exp. Dates Feb 2018 - Nov 2018

Lot numbers: Product Code ASK-45703-PNHS: 23F16M0498 Product Code ASK-45703-PGMCL: 23F17A0505 Product Code ASK-45703-PNW: 23F17B0116

Lot Numbers:
numbers
ASK-45703-PNHS
ASK-45703-PGMCL
ASK-45703-PNW
Product: Multi Lumen Central Venous Catheterization Kit; Product Code: ASK-12703-HH2; Exp. Dates Feb 2018 - Nov 2018

Lot number: 23F17C0652

Lot Numbers:
number
Product: Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter and Sharps Safety Features; Product Code: ASK-15703-PRWJ; Exp. Dates Feb 2018- Nov 2018

Lot number: 13F17C0400

Lot Numbers:
number
Product: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter, Sharps Safety Features, and Maximal Barrier Precautions Features; Product Code: ASK-12703-WMC1; Exp. Dates Feb 2018 - Nov 2018

Lot number: 23F17C0757

Lot Numbers:
number
Product: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product code: ASK-45703-PHF2; Exp. Dates Feb 2018 - Nov 2018

Lot number: 23F17D0182

Lot Numbers:
number
Product: Arrow Multi Lumen CVC Kit (Central venous catheter); Product Code: CDC-15703-1A; Exp. Dates Feb 2018 - Nov 2018

Lot number: 13F16M0241

Lot Numbers:
number
Product: AGB+ Multi Lumen Central Venous Catheterization Kit; Product Codes: CDC-42703-XP1A and CDC-47702-XP1A; Exp. Dates Feb 2018 - Nov 2018

Lot numbers: Product Codes CDC-42703-XP1A: 23F16M0507 Product Code CDC-47702-XP1A: 23F17A0533

Lot Numbers:
numbers
CDC-47702-XP1A
Product: ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter); Product Code: AK-45703-ACDC; Exp. Dates Feb 2018 - Nov 2018

Lot numbers: 13F17C0102 and 13F16M0264

Lot Numbers:
numbers
Product: Central Venous Catheterization Kit with Blue FlexTip Catheter; Product code: AK-04301; Exp. Dates Feb 2018 - Nov 2018

Lot number: 13F17C0501

Lot Numbers:
number
Product: ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume Infusions; Product Codes: AK-22142-CDC, AK-22142-F, AK-25142-CDC, AK-25142-F; Exp. Dates Feb 2018 - Nov 2018

Lot numbers: Product Code AK-22142-CDC: 13F17A0021 13F17A0315 Product Code AK-22142-F: 13F17B0338 13F17E0067 Product Code AK-25142-CDC: 13F17E0340 Product Code AK-25142-F: 13F17A0207

Lot Numbers:
numbers
AK-22142-CDC
AK-22142-F
AK-25142-CDC
AK-25142-F

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79197
Status: Resolved
Manufacturer: Arrow International Inc
Manufactured In: United States
Units Affected: 12 products (5,926 total)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.