Recall Atlas
Drugs & medicalClass II

Digisonics, Inc recalls Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound reporting software

Software issue

Read the official notice →
Date
2023-07-26
Country
United States
Brand
Digisonics, Inc
Product
Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound reporting software
Classification
Class II
Units
US Distribution: AK, NH, WY, TX, NE, CA, MD, TX, OR IA, IL, MO, OR, NY, UT,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2023-08-02
  2. US
    Drugs & medicalClass II

    ALEMBIC PHARMACEUTICALS, INC. recalls Diclofenac Sodium Topical Solution USP, 2% w/w, 3.8 FL.OZ.(112 grams) bottles, Rx only, Manufactured for: Alembic Pharmaceuticals,…

    Defective Delivery System

    FDA · DrugALEMBIC PHARMACEUTICALS, INC.Nationwide within the United StatesOfficial notice →
  3. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Methylphenidate Hydrochloride Tablets, USP 20mg, Rx Only, 100 Tablets per bottle, Manufactured by: Ohm Laboratories Inc., New…

    Presence of Foreign Substance: Metal embedded in a tablet.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwideOfficial notice →
  4. US
    Drugs & medicalClass II

    Sagent Pharmaceuticals recalls Oxacillin for Injection, USP, 1 gram per vial, For IV or IM Use, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in…

    Lack of Assurance of Sterility

    FDA · DrugSagent PharmaceuticalsNationwide in the USAOfficial notice →
  5. 2023-07-26
  6. US
    Drugs & medicalClass II

    Materialise N.V. recalls MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched device designed to…

    The wrong tibia guide was included intended for a different patient case.

    FDA · DeviceMaterialise N.V.International Distribution to countries of: Germany, NetherlandsOfficial notice →
  7. US
    Drugs & medicalClass II

    UFSK - International OSYS Gmbh recalls UFSK Treatment chair 500 XLE- Treatment chair for positioning and support of the patient during diagnostic and therapeutic…

    Service life of the electrical seat part drive of the treatment chair may be shortened unexpectedly after several years of use due to a potential wear-related reduction in the self-locking of the drive and may remain…

    FDA · DeviceUFSK - International OSYS GmbhNationwideOfficial notice →
  8. US
    Drugs & medicalClass II

    Ascensia Diabetes Care US, Inc. recalls Contour¿ next GEN Blood Glucose Monitoring System

    Ascensia Diabetes Care has determined through customer complaints that 580 of 2900 meters from lot number DM01T033P are reconfigured from mg/dL to mmol/L. Among them, 579 meters distributed in the United States were…

    FDA · DeviceAscensia Diabetes Care US, Inc.Domestic: CA, CO, FL, IN, MO, NJ, NY, OH, RI, SC, TN, TX, & VA.Official notice →
See all drugs & medical recalls →