Bard Peripheral Vascular Inc 2026-02-25 Health serious FDA
Health · FDA · Recall #FDA-Z-1367-2026
Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff… Recall
Issued February 25, 2026 · Bard Peripheral Vascular Inc
In February 2026, Bard Peripheral Vascular Inc recalled the Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Due to damage to outer tray that can potentially compromise the sterile barrier
What you should do
- 1 Stop using Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Bard Peripheral 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
- Bard Peripheral Vascular Inc
- Category
- Health
- Recall date
- February 25, 2026
- Units affected
- Not reported
- Sold at
- Worldwide - U.S. Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA,
- Recall number
- FDA-Z-1367-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Bard Peripheral Vascular Inc has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.