Drugs & medicalClass II

Cardinal Health 200, LLC recalls Procedure pack: Presource PBDS Cat. PLMHCSBHF, Hermann Hospital MHHS, Kit, C Section B MHHS, Sterile.

Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).

Read the official notice →
Date
2023-10-18
Country
United States
Brand
Cardinal Health
Product
Procedure pack: Presource PBDS Cat. PLMHCSBHF, Hermann Hospital MHHS, Kit, C Section B MHHS, Sterile.
Classification
Class II
Units
Worldwide distribution - US Nationwide distribution in the states of AZ, CA,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Cardinal Health recalls

  1. 2023-11-01
  2. US
    Drugs & medicalClass I

    Cardinal Health 200, LLC recalls Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack

    Demonstrated recognition and compatibility issues with syringe infusion pumps.

    FDA · DeviceCardinal Health 200, LLCUS Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID,…Official notice →
  3. 2023-10-25
  4. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777

    Syringe contains conical tip that is not compatible with certain needleless IV connector(s).

    FDA · DeviceCardinal Health 200, LLCNationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL,…Official notice →
  5. 2023-10-18
  6. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Procedure packs: (1) Presource PBDS Cat. PN33BPCR2, Kit, Back, Sterile; (2) Presource PBDS Cat. POCGANA11, Kit, ARN Anterior Hip,…

    XXX

    FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →
  7. 2023-07-26
  8. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls NovaPlus Infant Heel Warmer, Instant Squeeze Activation, Catalog Number V11460-010

    Cardinal Health has received an increase in burst/leaking complaints from mid-April to May regarding the above listed lot of the Novalplus Infant Heel Warmer with tape.

    FDA · DeviceCardinal Health 200, LLCUS Nationwide distribution.Official notice →
  9. 2023-06-14
  10. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Presource Kit, SMA21LPUHJ GYN Laparoscopy Pack. Convenience kit used for Laparoscopic surgery

    Inadvertently released for distibution without sterility assurance.

    FDA · DeviceCardinal Health 200, LLCDistribution in the US to GeorgiaOfficial notice →
  11. 2023-03-01
  12. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Cardinal Health Presource Packs IV START TRAY I-Intended for IV access device CATALOG #: 01-5799A

    Presource Kits contains the ICU MicroClave Clear Connector due to a manufacturing defect there is a gap between the connectors top and bottom housings which may lead to fluid leaks and loss of fluid path integrity

    FDA · DeviceCardinal Health 200, LLCUS Nationwide distribution in the states of GA, PA.Official notice →
All 41 Cardinal Health recalls →

Other drugs & medical recalls in the United States

  1. 2023-10-18
  2. US
    Drugs & medicalClass II

    Advance-Esthetic LLC recalls MED-810A Zemits NDPrime Laser products

    Advance-Esthetic LLC failed to comply with the applicable standards regarding Electronic Product Radiation Control (EPRC) regulations associated with the laser product performance standards and certification. This…

    FDA · DeviceAdvance-Esthetic LLCUS Nationwide DistributionOfficial notice →
  3. US
    Drugs & medicalClass II

    CareFusion 303, Inc. recalls BD Pyxis CII Safe ES, REF: 1116-00; and BD Pyxis : CII Safe ES Desktop PC, Wired SCNR, REF: 107-254-01; CII Safe ES Desktop PC, W-LESS…

    When global edit is used to update multiple formulary properties simultaneously, the following properties: 1) Require Lot Number on Recall, 2) Access Destruction Bin (Witness), 3) Add to Destruction Bin (Count/Empty),…

    FDA · DeviceCareFusion 303, Inc.US Nationwide distribution in the states of LA, NC, NY, MI, MA, NV, KS, IA, CA.Official notice →
  4. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Procedure packs: (1) Presource PBDS Cat. PN33BPCR2, Kit, Back, Sterile; (2) Presource PBDS Cat. POCGANA11, Kit, ARN Anterior Hip,…

    XXX

    FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →
  5. US
    Drugs & medicalClass II

    RoyalVibe Health Ltd. recalls CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water Restructuring Pad, RoyalVibe…

    Ultrasound devices were not authorized, cleared, or approved by FDA, and thus their performance characteristics have not been adequately established. There is a possibility of customers' reliance on marketing claims…

    FDA · DeviceRoyalVibe Health Ltd.US: MI, PA, TX, GA, OH, CA, FL, NY, NH, UT, AL, WA. WI, MN, MA, NM, IA, MD,…Official notice →
  6. US
    Drugs & medicalClass II

    Smiths Medical ASD Inc. recalls Medfusion Syringe Pump, Model 3500-500, v3, v4, v5, and v6

    A force sensor in the occlusion detector may drift out of calibration leading to increased occlusion detection times, false occlusion alarms, or a System Failure Alarm. If the force sensor calibration shift is large…

    FDA · DeviceSmiths Medical ASD Inc.Worldwide distribution - US Nationwide and the country of Canada.Official notice →
  7. US
    Drugs & medicalClass II

    Flower Orthopedics Corporation recalls Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used to ream and subsequently open the intramedullary canal to…

    Device is breaking while in use, potential for patients to require a revision surgery.

    FDA · DeviceFlower Orthopedics CorporationUS Nationwide distribution.Official notice →
See all drugs & medical recalls →