FDAFDA · Food and drugs·Recall number Z-0295-2021
Bard 3F SL PowerMidline Full Kit CE-indicated for short term access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media Ref: P6153208
Published November 4, 2020 · Recall initiated: September 14, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Kits do not contain the stylet/T-lock assembly indicated as a component on the label, may lead to a procedural delay and possibly discard of the kit.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Becton Dickinson & Company
- Distributor
- Foreign: Italy, Spain, and UK
- Lot
- Lot Number: REEQ3598 Feb-2022 and REER0518 Mar-2022 UDI: 00801741141065
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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