Bard Access Systems, Inc. 2026-07-08 Health serious FDA
Health · FDA · Recall #FDA-Z-2656-2026
CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 … Recall
Issued July 8, 2026 · Bard Access Systems, Inc.
In July 2026, Bard Access Systems, Inc. recalled the CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 …, a serious health recall reported by the FDA.
Compiled by Dana Whitfield, RecallCheckr
What this means for you
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
What you should do
- 1 Stop using CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 … right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Bard Access Systems, 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
- Bard Access Systems, Inc.
- Category
- Health
- Recall date
- July 8, 2026
- Units affected
- Not reported
- Sold at
- Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA
- Recall number
- FDA-Z-2656-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Bard Access Systems, Inc. has 2 recalls in our database.
- We're tracking 3,673 Health recalls in our database.
- This is the 453rd Health recall we've logged in 2026.