Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GuardIVa Antimicrobial Hemostatic IV Dressing Recalled by Bard Access Systems Due to Bard Access Systems is recalling GuardIVa (Ref. No....
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Bard Access Systems directly.
Affected Products
GuardIVa Antimicrobial Hemostatic IV Dressing, REF FP-23-AD008, Manufacturer: Bard Access Systems, Inc. USA. Product Code FP23AD006.
Quantity: 2532 units
Why Was This Recalled?
Bard Access Systems is recalling GuardIVa (Ref. No. FP23AD006) from lot ASXHT003 because they were non-sterile unit samples which potentially could be used clinically.
Where Was This Sold?
This product was distributed to 4 states: AR, LA, OK, TX
About Bard Access Systems
Bard Access Systems has 24 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report