Drugs & medicalClass II

Fisher Diagnostics recalls Pacific Hemostasis Thromboplastin-D, 4 ml. Used in performing one-stage prothrombin time test and factor assays.

The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.

Read the official notice →
Date
2025-04-09
Country
United States
Brand
Fisher Diagnostics
Product
Pacific Hemostasis Thromboplastin-D, 4 ml. Used in performing one-stage prothrombin time test and factor assays.
Classification
Class II
Units
US Distribution to: PA and OUS Foreign country of: United Arab Emirates.
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2025-04-09
  2. US
    Drugs & medicalClass II

    PYRAMES INC recalls Boppli: Bedside Device Kit, REF: 54-0002; Sensor Band, REF: 51-0007

    Single-use battery-powered blood pressure monitor, for use on neonates and infants, due to vibratory noise, may not adequately detect changes in blood pressure per specification. Containment actions: 1) Ventilator…

    FDA · DevicePYRAMES INCUS distribution to states of: MA and CAOfficial notice →
  3. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.

    Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.

    FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide and the countries of Austria, Belgium,…Official notice →
  4. US
    Drugs & medicalClass II

    Qiagen Sciences LLC recalls Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference Number (REF): 691224 Software Version: n/a Component: n/a

    Identified faulty cartridges. If such a faulty cartridge is used for sample testing, false test results could occur.

    FDA · DeviceQiagen Sciences LLCUS Distribution: AL, CA, DC, FL, IN, KS, KY, MA, ME, MN, NY, and TX.Official notice →
  5. US
    Drugs & medicalClass II

    Reichert, Inc. recalls Phoroptor VRx Digital Refraction System Model Numbers: 16241

    The head of the phoropter head could come loose and potentially detach due to a default in the assembly.

    FDA · DeviceReichert, Inc.Domestic: Nationwide Distribution. International: Austria, Bolivia, Canada,…Official notice →
  6. US
    Drugs & medicalClass I

    Draeger, Inc. recalls Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description:…

    The potential for cracks forming in the breathing circuit hose.

    FDA · DeviceDraeger, Inc.Domestic: Nationwide Distribution. International - following countries:…Official notice →
  7. US
    Drugs & medicalClass II

    Terumo Cardiovascular Systems Corporation recalls Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Catalog Number REF CD1754

    During some clinical cases, it has been observed that the SO2 value may periodically appear as dashes on the Touchscreen Display indicating unavailable data. In these cases, a yellow low-limit alarm will also be…

    FDA · DeviceTerumo Cardiovascular Systems CorporationUS: IL, TX, NY, MI, FL, NV, and Australia, New ZealandOfficial notice →
See all drugs & medical recalls →