Drugs & medicalClass I

National Distribution & Contracting Inc recalls ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl

Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.

Read the official notice →
Date
2021-10-20
Country
United States
Brand
National Distribution & Contracting Inc
Product
ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl
Classification
Class I
Units
Worldwide distribution - US Nationwide distribution including in the states of…
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2021-10-20
  2. US
    Drugs & medicalClass II

    Bio-Rad Laboratories, Inc. recalls BioPlex 2200 ANA Screen Control Set, REF: 663-1131 incompatible with ANA Screen Reagent Packs/ANA Kits, REF: 665-1150; and ANA Screen…

    A new lot of ANA screen control and any subsequent control lots are incompatible with older lot numbers of ANA calibrators and ANA reagent packs.

    FDA · DeviceBio-Rad Laboratories, Inc.Worldwide distribution - U.S Nationwide distribution including in the states…Official notice →
  3. US
    Drugs & medicalClass II

    Philips North America LLC recalls Philips, HeartStart HS1 OnSite Defibrillator, Model #'s: M5066A and M5067A

    Customers were not notified of previous recalls associated with various defibrillator models.

    FDA · DevicePhilips North America LLCU.S.: CA, CT, FL, GA, IN, MI, MO, NJ, NY, OH, TX, and WA. International…Official notice →
  4. US
    Drugs & medicalClass II

    W L Gore & Associates, Inc. recalls Heparin, GORE VIABAHN VBX, BALLOON EXPANDABLE ENDOPROTHESIS, REF BXAL085902E, 8 MM X 59 MM 8 Fr, LARGE BALLOON EXPANDLBE, Nominal…

    Incorrect labeling, specifically, expandable endoprosthesis labeled as 8 mm x 59mm x 135 cm, however may contain a 9mm x 29 mm x 135 cm device.

    FDA · DeviceW L Gore & Associates, Inc.International distribution to the countries of Italy & Lebanon.Official notice →
  5. US
    Drugs & medicalClass I

    Abbott Molecular, Inc. recalls Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic

    There is a potential for false positive results.

    FDA · DeviceAbbott Molecular, Inc.Worldwide Distribution. US Nationwide, AUSTRALIA, AUSTRIA, BELGIUM, BRAZIL,…Official notice →
  6. US
    Drugs & medicalClass I

    Eli Lilly & Company recalls Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection, 1 mg per vial; Diluent for Glucagon, 1 mL syringe. Rx only, Marketed…

    SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected powder substance. There was also a lack of full drug effect upon administration.

    FDA · DrugEli Lilly & CompanyNationwide with the USA and Puerto Rico; Canada, Argentina, Costa Rica, MexicoOfficial notice →
  7. US
See all drugs & medical recalls →