Drugs & medicalClass II

Bard Peripheral Vascular Inc recalls BARD MAGNUM Disposable Core Tissue Biopsy Needle REF: MN1410 MN 1420 MN1610 MN1616 MN1820 MN2010 The Magnum Biopsy System…

Due to possible packaging damage (indentations/cuts) cause by manufacturing process. As a result of the packaging damage, may cause the sterile barrier to be compromised.

Read the official notice →
Date
2024-10-02
Country
United States
Brand
Bard Peripheral Vascular
Product
BARD MAGNUM Disposable Core Tissue Biopsy Needle REF: MN1410 MN 1420 MN1610 MN1616 MN1820 MN2010 The Magnum Biopsy System (instrument and…
Classification
Class II
Units
Worldwide - U.S. Nationwide distribution in the Puerto Rico and the countries…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Bard Peripheral Vascular recalls

  1. 2025-03-12
  2. US
    Drugs & medicalClass I

    Bard Peripheral Vascular Inc recalls Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF: 80237; S 8 F…

    Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps intended to reduce the likelihood of catheter breakage events. Catheter has an outer cylinder connected to a rotating helix, which could…

    FDA · DeviceBard Peripheral Vascular IncUS Nationwide Distribution: NY, VA, KY, IN, OR, FL, MD, NJ, LA, CO, PR, PA,…Official notice →
  3. 2024-11-27
  4. US
    Drugs & medicalClass II

    Bard Peripheral Vascular Inc recalls Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10 CM, REF:…

    Disposable biopsy instruments were potentially manufactured missing the backend notch retention feature on the needle that results in inadequate securing of the needle inside the device, which could lead to needle…

    FDA · DeviceBard Peripheral Vascular IncWorldwide - US Nationwide including in the states of WA, LA, MN, PA, UT, SC,…Official notice →
  5. 2024-11-20
  6. US
    Drugs & medicalClass II

    Bard Peripheral Vascular Inc recalls The EVSRF catheter is a sterile, single-use disposable medical device for endovenous radiofrequency ablation, a procedure in which a…

    The Venclose" RF Ablation Catheters may have been manufactured with internal wiring error. The red and yellow signal wires were soldered on swapped ports of the catheter PCB. This error in wire configuration would lead…

    FDA · DeviceBard Peripheral Vascular IncWorldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →
  7. 2024-09-18
  8. US
    Drugs & medicalClass II

    Bard Peripheral Vascular Inc recalls Guidewire 70cm x 1mm (0.038 ) REF 5583705 These accessories are intended for use with Bard 14.5 Fr. Long-Term Dual Lumen…

    Due to guidewires being manufactured incorrectly with the guidewires being mis-assembled within the hoop such that the proximal (stiff) end of the guidewire is located at the distal end of the hoop. Injury could occur…

    FDA · DeviceBard Peripheral Vascular IncWorldwide - U.S. Nationwide distribution in the states of OH, TX, and WV. The…Official notice →
  9. 2024-01-17
  10. US
    Drugs & medicalClass II

    Bard Peripheral Vascular Inc recalls BD Recanalization System, REF: BDRECANSYSTEM

    Recanalization systems may be in a manufacturing mode that allows the system to continuously run without the typical 30 second pauses, and 4-minute warning/5-minute restart required messages to indicate the ten-minute…

    FDA · DeviceBard Peripheral Vascular IncUS: CA, OH, PA, NY, TX, NJ, MS, IL, GA, AL, AZ, NC, NV, PR, IN, MA, WI, KS,…Official notice →
  11. US
    Drugs & medicalClass II

    Bard Peripheral Vascular Inc recalls Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit 14G x 16CM;…

    The internal diameter of the coaxial cannula may be smaller or larger than the external diameter of the biopsy needle, and the length of the cannula may exceed the stated length on the label. As a result, the biopsy…

    FDA · DeviceBard Peripheral Vascular IncWorldwide - US Nationwide distribution including in the states of PR, IL, MA,…Official notice →
All 20 Bard Peripheral Vascular recalls →

Other drugs & medical recalls in the United States

  1. 2024-10-02
  2. US
    Drugs & medicalClass II

    Centinel Spine, Inc. recalls prodisc C SK, Total cervical disc replacement, medical device, Model/Catalog Number: PDSM5

    During the assembly of Prodisc C, a blue discoloration was observed on a Prodisc C inlay. The discoloration is considered a foreign contaminate that may not have been fully evaluated in the manufacturing validations.

    FDA · DeviceCentinel Spine, Inc.US Nationwide distribution.Official notice →
  3. US
    Drugs & medicalClass II

    Stryker Spine recalls AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion…

    Labeling Correction: Instructions For Use (IFU)-Updated electronic Rev 5, specific language for indications for use for the United States and Canada was inadvertently removed.

    FDA · DeviceStryker SpineWorldwide distribution - US Nationwide and the country of Canada.Official notice →
  4. US
    Drugs & medicalClass II

    Microcare Medical recalls Good Vibrations Ultrasonic Cleaner Solution, JorVet J0382G Ultrasonic Instrument Cleaning Solution, SpecClean Ultrasonic Cleaner Solution,…

    Contaminated equipment and packaging caused Klebsiella oxytoca, Enterobacter asburiae, Enterobacter bugandensis, pathogenic and opportunistic bacteria, to occur in ultrasonic detergent, which caused product…

    FDA · DeviceMicrocare MedicalWorldwide - US Nationwide distribution in the states of MN, GA, PA, WA, CO,…Official notice →
  5. US
    Drugs & medicalClass II

    Philips North America Llc recalls Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal…

    Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and protrude beyond the surface could cause the screws to interfere with other moving parts, potentially blocking the horizontal tabletop. May…

    FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of Argentina,…Official notice →
  6. US
    Drugs & medicalClass II

    Argon Medical Devices, Inc recalls BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-1580-01, 360-1580-02, 360-1580-03,…

    Holes have been identified in biopsy instrument packaging trays compromising the sterile barrier, which may lead to cross contamination, or the introduction of micro-organisms into the access site, which could lead to…

    FDA · DeviceArgon Medical Devices, IncWorldwide - US Nationwide distribution including in the states of AZ, FL, OH,…Official notice →
  7. US
    Drugs & medicalClass II

    Merit Medical Systems, Inc. recalls Custom Procedure Kit, REF: K12T-11077

    7F sheath introducers labeled as 7.5F

    FDA · DeviceMerit Medical Systems, Inc.Worldwide - US Nationwide distribution in the states of WI, MN, TX, PA, GA,…Official notice →
See all drugs & medical recalls →