Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Recalled by Bard Medical Division Due to Medline notified BMD that the Aplicare Povidone Iodine...
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 Medical Division directly.
Affected Products
Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product Packaging: Three (3) PVP-I prep pads are packed into each urine collection kit carton along with a pre-connected drainage funnel, specimen container, funnel lid, specimen lid and a room label.
Quantity: 131,950
Why Was This Recalled?
Medline notified BMD that the Aplicare Povidone Iodine (PVP-I) Prep Pads were not meeting the iodine assay level requirements to support 36 month expiration dating.
Where Was This Sold?
This product was distributed to 24 states: AR, CA, CO, FL, GA, IL, IN, IA, KS, LA, MD, MA, MI, MN, MS, MO, NJ, NY, NC, SC, TN, TX, UT, WA
About Bard Medical Division
Bard Medical Division has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report