ARROW INTERNATIONAL Inc. 2023-09-27 Health serious FDA
Health · FDA · Recall #FDA-Z-2590-2023
Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter,… Recall
Issued September 27, 2023 · ARROW INTERNATIONAL Inc.
In September 2023, ARROW INTERNATIONAL Inc. recalled the Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter,…, a serious health recall reported by the FDA.
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 Stop using Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact ARROW INTERNATIONAL Inc. to arrange your voluntary. See the official notice below for contact details.
- 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
- September 27, 2023
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-2590-2023
- 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.