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
Reported: November 4, 2020 Initiated: September 14, 2020 #Z-0295-2021
Product Description
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
Reason for Recall
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.
Details
- Recalling Firm
- Becton Dickinson & Company
- Units Affected
- 72 units
- Distribution
- Foreign: Italy, Spain, and UK
- Location
- Franklin Lakes, NJ
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Becton Dickinson & Company. Units affected: 72 units.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 4, 2020. Severity: Moderate. Recall number: Z-0295-2021.
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