Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2943-2018 — 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.

U.S. FDA — Device Enforcement · United States · 2018-03-21 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2943-2018
Date of alert: 2018-03-21
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Bard Medical Division
Product category: device
Product type: Devices

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-2943-2018 — 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.

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