Bard 3F SL PowerMidline Full Kit CE-indicated for short recall
Bard 3F SL PowerMidline Full Kit CE-indicated for short term access to the peripheral venous system for selected intravenous therapies, blood…
Why was Bard 3F SL PowerMidline Full Kit CE-indicated for short recalled?
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 should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Number: REEQ3598 Feb-2022 and REER0518 Mar-2022 UDI: 00801741141065
- Product
- Bard 3F SL PowerMidline Full Kit CE-indicated for short term access to the peripheral venous system for selected intravenous therapies, blood…
- Recalling firm
- Becton Dickinson & Company
- Quantity
- 72 units
- Distribution
- Foreign: Italy, Spain, and UK
- Recall date
- November 4, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)