Drugs & medicalClass II

CareFusion 303, Inc. recalls BD Pyxis MedBank MedPass Software, REF: 139088-01

After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which could lead to…

Read the official notice →
Date
2023-10-04
Country
United States
Brand
CareFusion
Product
BD Pyxis MedBank MedPass Software, REF: 139088-01
Classification
Class II
Units
US: FL, MI, KS
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 Details may be shortened or out of date; the official notice is the authoritative source.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 CareFusion recalls

  1. 2024-03-13
  2. US
    Drugs & medicalClass II

    CareFusion 303, Inc. recalls BD Pyxis: MedStation ES, REF: 323; Anesthesia Station ES, REF: 327; MedStation ES Tower, REF: 352;

    Automated dispensing cabinets, running affected software, and Windows 10 operating system may experience the application randomly hang, freeze and/or crash, which may result in delays in medication access, and…

    FDA · DeviceCareFusion 303, Inc.Worldwide distribution - US Nationwide distribution including in the states of…Official notice →
  3. 2023-11-15
  4. US
    Drugs & medicalClass I

    CareFusion 303, Inc. recalls Alaris PCA Module 8120

    Alaris PCA Module 8120, Patient Controlled Analgesia infusion pump: compatible syringes labeling contains syringes that have not been validated.

    FDA · DeviceCareFusion 303, Inc.Worldwide Distribution: US (nationwide): AK, AL, AR, AS, AZ, CA, CO, DC, DE,…Official notice →
  5. 2023-10-18
  6. 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 →
  7. 2023-09-27
  8. US
    Drugs & medicalClass II

    CareFusion 213, LLC recalls BD ChloraPrep Clear, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Sterile Solution, 0.03mL (1 ml) each, 60…

    Stability data does not support expiry: Shelf-life of the impacted lots of BD ChloraPrep" Clear 1 mL Applicator cannot be substantiated beyond 12-months although labeled with 36-month expiry. Stability studies indicate…

    FDA · DrugCareFusion 213, LLCDistributed nationwide to 100 consignees. Please refer to consignee list.Official notice →
  9. 2023-08-23
  10. US
    Drugs & medicalClass II

    Carefusion 2200 Inc recalls Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 50 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7045; endoscopic surgical device

    Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.

    FDA · DeviceCarefusion 2200 IncUS and CanadaOfficial notice →
  11. 2023-07-12
  12. US
    Drugs & medicalClass II

    CareFusion 303, Inc. recalls BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223, 107-224, 111-191,…

    Automated dispensing cabinet devices plugged into any multi-socket outlet power strips may present unacceptable levels of current leakage, which could expose users to system downtime and/or potential electric shock.

    FDA · DeviceCareFusion 303, Inc.US Nationwide-Worldwide Distribution: CO, MS, HI, FL, GA, CA, ND, GU, DE, MO,…Official notice →
All 64 CareFusion recalls →

Other drugs & medical recalls in the United States

  1. 2023-10-11
  2. US
    Drugs & medicalClass II

    Central Admixture Pharmacy Services Inc recalls fentaNYL, 100 mcg/2 mL, (50 mcg/mL), 3 mL Syringe, Rx only, Repackaged by CAPS Inc., 7935 Dunbrook Road, Suite C, San…

    Lack of assurance of sterility:

    FDA · DrugCentral Admixture Pharmacy Services IncNationwide in the USAOfficial notice →
  3. 2023-10-05
  4. US
    Drugs & medical

    CURiO Recalls Capri Blue Pet Products Due to Risk of Exposure to Bacteria (Recall Alert)

    The recalled pet products can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are…

    CPSCAbout 59,000Official notice →
  5. 2023-10-04
  6. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.

    Epiphany, now a Baxter Healthcare company, is issuing an Urgent Medical Device Correction for the Cardio Server E3 ECG Management System software listed below due to a report of the caliper tool becoming…

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide distribution including in the states of…Official notice →
  7. US
    Drugs & medicalClass II

    Stryker Corporation recalls Cinchlock SS Knotless Anchor Inserter, Part Number CAT02462

    Expired Product distributed

    FDA · DeviceStryker CorporationUS Nationwide distribution in the states of NY, NC, GA, TN, KY, IL, UT, AZ,…Official notice →
  8. US
    Drugs & medicalClass II

    B. Braun Medical, Inc. recalls B.Braun NORM-JECT Luer Lock Solo, 10 ml, Sterile-Intended to be used to deliver (inject) or withdraw an accurate metered dose of a fluid…

    The sterile blister packaging may be damaged, and sterility may be compromised

    FDA · DeviceB. Braun Medical, Inc.US Nationwide distribution in the state of VA.Official notice →
  9. US
    Drugs & medicalClass II

    Wolf, Henke Sass, Gmbh recalls Henke-Ject-2 part luer sterile single use syringes - used for intravenous, intramuscular, subcutaneous, intracutaneous and intraarterial…

    Sterile barrier might be damaged compromising the sterility of the device.

    FDA · DeviceWolf, Henke Sass, GmbhWorldwide distribution - US Nationwide and the country of Canada.Official notice →
See all drugs & medical recalls →