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.

Read the official notice →
Date
2023-11-01
Country
United States
Brand
Cardinal Health
Product
Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack
Classification
Class I
Units
US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2024-02-14
  2. US
    Drugs & medicalClass I

    Cardinal Health 200, LLC recalls Cardinal Health Monoject, 35mL Enteral Syringe (purple) - For Use with ENFit Connection System, REF 435SE

    The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6, 12, 35, 60 mL) have recognition and compatibility issues with certain syringe enteral feeding pumps. As a result, Cardinal Health recommends…

    FDA · DeviceCardinal Health 200, LLCDistribution US nationwide and Canada. Foreign distribution updated 9/6/2024…Official notice →
  3. 2024-01-24
  4. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls CardinalHealth Suction Canister Liner, MEDI-VAC CRD, REF 65651-510

    The above-listed lots of Cardinal Health Medi-Vac CRD" Suction Canister Liners 1L may experience loss of suction on low or low intermittent suction settings, due to a misalignment of the liner with the outer hard…

    FDA · DeviceCardinal Health 200, LLCUS, Canada, Australia and New ZealandOfficial notice →
  5. 2023-11-29
  6. US
    Drugs & medicalClass I

    Cardinal Health Inc. recalls LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Propylene Glycol, 0.3%); 0.33 FL OZ (10 mL) dropper bottle, Sterile,…

    Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.

    FDA · DrugCardinal Health Inc.Nationwide in the USAOfficial notice →
  7. 2023-10-25
  8. 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 →
  9. 2023-10-18
  10. 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 →
  11. US
    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).

    FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →
All 41 Cardinal Health recalls →

Other drugs & medical recalls in the United States

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

    Omega Medical Imaging, Inc. recalls Omega Medical Imaging Elevating Monitor Suspension, Part Number 1000-0085

    An actuator separated from the pivot mechanism on a lower monitor boom system column and became detached and was restrained by the installed safety cable at one location.

    FDA · DeviceOmega Medical Imaging, Inc.Worldwide distribution - US Nationwide and the country of Pakistan.Official notice →
  3. US
    Drugs & medicalClass II

    Impedimed Limited recalls SOZO Bilateral Arm L-Dex Software

    Bilateral L-Dex assessment software does not have the same level of sensitivity to help detect early signs of lymphedema as the unilateral arm L-Dex assessment, which could result in under-recognition of early…

    FDA · DeviceImpedimed LimitedUS Nationwide distribution in the states of IA, CA, IL, AK, NY, FL, KS, WI,…Official notice →
  4. US
    Drugs & medicalClass II

    Preat Corp recalls Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental

    The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage

    FDA · DevicePreat CorpUS: FL, CA, OR, TX, OH, CA, SC, OR, NJ, SC, OUS: NoneOfficial notice →
  5. US
    Drugs & medicalClass II

    GE Healthcare recalls Universal Viewer Workflow Manager, Image processing radiological system

    When using Universal Viewer or Centricity Universal Viewer with Workflow Manager (WFM), if a third-party reporting application is used to launch exams, it could display information on a different patient than WFM and…

    FDA · DeviceGE HealthcareNationwide distribution to AR, AZ, CA, CO, DE, FL, GA, IL, IN, ME, MI, MN, MO,…Official notice →
  6. US
    Drugs & medicalClass II

    Smiths Medical ASD Inc. recalls Portex Pro-Vent Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, REF 4599P-1

    The complaint involved the absence of a component called "ASM Filter-Pro ABG SYR CAP" from the packaging of Pro-Vent Arterial Blood Sampling (ABG) Kits. Specifically, this issue affected a total of 31,900 kits under…

    FDA · DeviceSmiths Medical ASD Inc.USOfficial notice →
  7. US
    Drugs & medicalClass II

    GE Healthcare recalls Centricity PACS-IW with Universal Viewer, versions 5.0 SPx with PACS-IW foundation; Radiological Image Processing System

    GE HealthCare has become aware of an issue where images from two different patients may be contained in a single study, when stored in Centricity PACS-IW V3.7.x, Centricity PACS-IW with Universal Viewer V5.0 and…

    FDA · DeviceGE HealthcareUS and Austria, Azerbaijan, Bosnia and Herzegovina, Brazil, Canada, Chile,…Official notice →
See all drugs & medical recalls →