Drugs & medicalClass II

Baxter Healthcare Corporation recalls Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009

The door on the Spectrum IQ Infusion pump may not be able to fully close.

Read the official notice →
Date
2024-11-20
Country
United States
Brand
Baxter Healthcare
Product
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
Classification
Class II
Units
GA, 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Baxter Healthcare recalls

  1. 2025-01-08
  2. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2

    Devices were identified as released after repair without full testing being performed, which includes flow testing.

    FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of AL, IN.Official notice →
  3. 2024-12-04
  4. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis

    There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution.Official notice →
  5. 2024-11-27
  6. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis

    Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using…

    FDA · DeviceBaxter Healthcare CorporationWorldwide Distribution (US Nationwide distribution)Official notice →
  7. 2024-11-20
  8. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Baxter AK 98 Dialysis Machine, Hemodialysis Delivery System, Product Code 955607. As of February 2025, the firm name is Vantive.

    Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using…

    FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution and worldwideOfficial notice →
  9. 2024-11-13
  10. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Hillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph

    There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to…

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution.Official notice →
  11. US
All 123 Baxter Healthcare recalls →

Other drugs & medical recalls in the United States

  1. 2024-11-20
  2. US
    Drugs & medicalClass II

    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Zenition 50, Model Number: 718096

    Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.

    FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Worldwide distribution - US Nationwide and the countries of Albania, Algeria,…Official notice →
  3. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog Number: WA22810A Software Version: N/A Product…

    Olympus is removing the statement of compatibility with a GreenLight Laser for BPH therapy from the Instruction for Use (IFU) due to the potential for a damaged tip during use of a laser probe.

    FDA · DeviceOlympus Corporation of the AmericasUS Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO,…Official notice →
  4. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003A

    Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of TN.Official notice →
  5. US
    Drugs & medicalClass II

    Cook Incorporated recalls Approach Hydro ST Micro Wire Guide; Catalog prefix HMW Reference Part Numbers: HMW-14-135-ST HMW-14-190-ST HMW-14-300-ST

    Affected device lots have labels that state the incorrect expiration dates.

    FDA · DeviceCook IncorporatedWorldwide - US Nationwide distribution.Official notice →
  6. US
    Drugs & medicalClass II

    The Metrix Company recalls SECURE 250 mL EMPTY EVA CONTAINER With 2 Ports, REF 66045; An empty single-use pouch made of plastic intended to contain a fluid for…

    A limited number of IV bags have been found to leak during filling.

    FDA · DeviceThe Metrix CompanyWorldwide - US Nationwide distribution in the states of TX, IL, OH, PA, WA,…Official notice →
  7. US
    Drugs & medicalClass II

    WISSNER-BOSSERHOFF GMBH recalls SafeControl handset (a component of the Sentida bed which moves and positions the bed), Model Numbers: 01-011539, 01-011541, 01-01198

    When the handset is disconnected from the power mains, and mains operation is restored, the handset is reset to the preset Resident mode. In this mode, the backrest, legrest, and height adjustment can be moved.

    FDA · DeviceWISSNER-BOSSERHOFF GMBHUS Nationwide distribution in the states of NC.Official notice →
See all drugs & medical recalls →