Access Vascular, Inc 2023-02-22 Health serious FDA
Health · FDA · Recall #FDA-Z-1130-2023
HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002 Recall
Issued February 22, 2023 · Access Vascular, Inc
In February 2023, Access Vascular, Inc recalled the HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Select catheter lots were identified to be labeled with incorrect expiration date, where the catheters expire prior to the labeled expiration date of the kit.
What you should do
- 1 Stop using HydroPICC 4Fr Single Lumen, 80cm Guidewire - Basic Kit, Model Number 80001002 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Access Vascular, 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
- Access Vascular, Inc
- Category
- Health
- Recall date
- February 22, 2023
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of CT, IL, IN, MA, NE, TN, and TX.
- Recall number
- FDA-Z-1130-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Access Vascular, Inc has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.