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Critical recall: Death or serious injury has been reported or is considered likely. Stop using this product now.

ARROW INTERNATIONAL Inc. 2023-10-11 Health critical FDA
Health · FDA · Recall #FDA-Z-0004-2024

Arrow ErgoPack Pressure Injectable Arrowg+ard Blue Advance Three-Lumen PICC pre-loaded… Recall

Issued October 11, 2023 · ARROW INTERNATIONAL Inc.

In October 2023, ARROW INTERNATIONAL Inc. recalled the Arrow ErgoPack Pressure Injectable Arrowg+ard Blue Advance Three-Lumen PICC pre-loaded…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.

What you should do

  1. 1 Stop using Arrow ErgoPack Pressure Injectable Arrowg+ard Blue Advance Three-Lumen PICC pre-loaded… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact ARROW INTERNATIONAL Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
ARROW INTERNATIONAL Inc.
Category
Health
Recall date
October 11, 2023
Units affected
Not reported
Sold at
US
Recall number
FDA-Z-0004-2024
Made in
United States
Issuing agency
FDA

In context

  • ARROW INTERNATIONAL Inc. has 5 recalls in our database, including 4 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 903rd Health recall we've logged in 2023.
Read the official FDA notice

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