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Get the free Bard® Magnum™ Biopsy Needle Recall Notice - mhra gov

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This document is to inform healthcare facilities about a voluntary recall of the Bard® Magnum™ Biopsy Needle due to a discrepancy in needle length, which may pose risks to patients. It outlines
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How to fill out Bard® Magnum™ Biopsy Needle Recall Notice

01
Obtain the Bard® Magnum™ Biopsy Needle Recall Notice form.
02
Fill in your contact information, including your name, address, and phone number.
03
Provide details about the specific biopsy needle lot number(s) you have.
04
Indicate how many devices are affected by the recall.
05
Include information about where and when you purchased the devices.
06
Sign and date the form to verify the information is accurate.
07
Submit the completed notice to the provided address or email.

Who needs Bard® Magnum™ Biopsy Needle Recall Notice?

01
Healthcare providers and facilities that have used Bard® Magnum™ Biopsy Needles.
02
Patients who have undergone procedures with the affected needles.
03
Distributors who have supplied these biopsy needles.
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People Also Ask about

Biopsies can sometimes cause bleeding, bruising, or swelling. This can make it seem like a lump is larger after the biopsy. Most often, this is nothing to worry about, and the bruising and swelling will go away over time.
Needle Gauge Chart Gauge NumberNeedle Nominal O.D. (mm)Needle Dead Volume (µL/25.4 mm) 18 gauge needle 1.27 14.011 µL/25.4 mm 17 gauge needle 1.473 22.715 µL/25.4 mm 16 gauge needle 1.651 28.444 µL/25.4 mm 15 gauge needle 1.829 37.529 µL/25.4 mm26 more rows
Additional information Weight0.1 lbs Dimensions 7.5 × 0.5 × 0.5 in Length 9cm Needle Type Biopsy Gauge 14G1 more row
Additional information Weight0.1 lbs Dimensions 15 × 4 × 0.75 in Length 10 cm Needle Type Soft Tissue Biopsy Gauge 18G1 more row
Gauge: 9 gauge. Length: 10 or 13 cm. Aperture: 12 mm. Throw/Stroke: 15 mm.
By convention, a fine needle is defined as a gauge of ≥22, corresponding to an outer diameter of ≤0.72 mm. In some instances, a larger needle (21-gauge or 18-gauge) is used, such as for endobronchial ultrasound-guided transbronchial needle aspiration or endoscopic ultrasound-guided FNA (EUS-FNA).
8:15 11:25 It is important to ensure both red markings are aligned as it will not deploy should this not be theMoreIt is important to ensure both red markings are aligned as it will not deploy should this not be the case the lesion or area of biopsy is then located and needle inserted. If using the marquee kit it

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The Bard® Magnum™ Biopsy Needle Recall Notice is an official notification regarding the recall of specific models of the Bard® Magnum™ Biopsy Needle due to safety concerns or defects.
Healthcare providers, distributors, and facilities that have used or received the recalled Bard® Magnum™ Biopsy Needle are required to file the notice.
To fill out the Bard® Magnum™ Biopsy Needle Recall Notice, individuals must provide relevant details such as the product's lot number, quantity on hand, and the reason for the return.
The purpose of the Bard® Magnum™ Biopsy Needle Recall Notice is to inform stakeholders about the recall, provide instructions for returning the product, and ensure patient safety.
The information that must be reported includes the product details, lot numbers, the number of devices affected, and contact information for follow-up.
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