Drugs & medicalClass II

Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4

Small patient labels do not match the primary device label. The primary device label accurately identifies the product as 4010-05-08-T4, while the smaller patient label incorrectly identifies the product as…

Read the official notice →
Date
2022-06-01
Country
United States
Brand
Devicor Medical Products
Product
HydroMARK Breast Biopsy Marker, Model No. 4010-05-08-T4
Classification
Class II
Units
US Nationwide distribution in the states of DE, KY, NY, OH, WV.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Devicor Medical Products recalls

  1. 2026-06-03
  2. US
    Drugs & medicalClass II

    Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3

    Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.

    FDA · DeviceDevicor Medical Products IncWorldwide distribution - US Nationwide and the countries of Canada, Singapore.Official notice →
All 2 Devicor Medical Products recalls →

Other drugs & medical recalls in the United States

  1. 2022-06-01
  2. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200

    The Implantable Neurostimulator (INS) cannot communicate with the clinical programmer and/or the patient programmer system.

    FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide distribution in the states of AK, AL,…Official notice →
  3. US
    Drugs & medicalClass II

    TELEFLEX MEDICAL INC recalls (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732, non-sterile; (3) Gibeck…

    Reports received of torn corrugated breathing tubes.

    FDA · DeviceTELEFLEX MEDICAL INCWorldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice →
  4. US
    Drugs & medicalClass III

    Microbiologics Inc recalls KWIK-STIK" plus: Clostridium perfringens

    Labeling error.

    FDA · DeviceMicrobiologics IncDistributed US Nationwide to IA, TN and internationally to Mexico, Colombia,…Official notice →
  5. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with Surescan MRI…

    The Implantable Neurostimulator Model may be susceptible to not communicating with the clinical programmer and/or patient programmer system.

    FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice →
  6. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls Olympus DISPOSABLE GRASPING FORCEPS, FG-51D

    Forceps do not comply with Olympus standards for the amount of force required to open and close the forceps

    FDA · DeviceOlympus Corporation of the AmericasUS Nationwide DistributionOfficial notice →
  7. US
    Drugs & medicalClass II

    Accriva Diagnostics, Inc. recalls The VerifyNow P2Y12 Test is designed to measure platelet P2Y12 receptor blockade. Substances known to specifically block the P2Y12…

    Two whole blood Platelet Reactivity tests exist that share the same reagent formulation and are used to obtain P2Y12 Reactivity Unit results. The test without US-FDA market clearance was distributed and it displays…

    FDA · DeviceAccriva Diagnostics, Inc.US Nationwide distribution in the state of California.Official notice →
See all drugs & medical recalls →