Drugs & medicalClass II

Family Dollar Stores, Llc. recalls QP COUGH COLD TABLET 16 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

Read the official notice →
Date
2022-08-31
Country
United States
Brand
Family Dollar Stores
Product
QP COUGH COLD TABLET 16 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Classification
Class II
Units
Nationwide within the United States
Category
Drugs & medical
Source
FDA · Drug

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 Details may be shortened or out of date; the official notice is the authoritative source.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 Family Dollar Stores recalls

  1. 2023-11-15
  2. US
    Drugs & medicalClass II

    Family Dollar Stores, Llc. recalls MEDIC's CHOICE CONTACT LENS SOLUTION 12FLOZ, SKU 998935

    Products were stored outside of labeled temperature requirements.

    FDA · DeviceFamily Dollar Stores, Llc.Distributed to Family Dollar stores in the following states: GA, AL, MS, FL,…Official notice →
  3. 2023-05-10
  4. US
    Drugs & medicalClass II

    Family Dollar Stores, Llc. recalls Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) 24-count Caplets

    CGMP deviation: product outside labeled storage temperature requirements.

    FDA · DrugFamily Dollar Stores, Llc.Nationwide within the United StatesOfficial notice →
  5. 2022-09-07
  6. US
    Drugs & medicalClass II

    Family Dollar Stores, Llc. recalls Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ. (59 g) UPC 0…

    cGMP deviation: Product held outside of appropriate temperature storage conditions.

    FDA · DrugFamily Dollar Stores, Llc.Distributed Nationwide in the USA to the following States: AZ, CA, GA, ID, IN,…Official notice →
  7. 2022-08-24
  8. US
    Drugs & medicalClass II

    Family Dollar Stores, Llc. recalls KY JELLY LUBRICANT 2 FL OZ, SKU 901443

    Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.

    FDA · DeviceFamily Dollar Stores, Llc.Product distributed to Family Dollar retail stores in US nationwide.Official notice →
  9. 2022-06-08
  10. US
    Drugs & medicalClass II

    Family Dollar Stores, Llc. recalls AMBI Skincare Fade Cream Oily Skin New & Improved, Net Wt. 2 OZ (56g)

    cGMP deviations: product stored outside of labeled temperature requirements.

    FDA · DrugFamily Dollar Stores, Llc.USA NationwideOfficial notice →
All 6 Family Dollar Stores recalls →

Other drugs & medical recalls in the United States

  1. 2022-08-31
  2. US
    Drugs & medicalClass I

    Hamilton Medical AG recalls HAMILTON-C6 Intensive Care Ventilator, REF: 160021

    Ventilator status indicator board can become loose, which could lead to water ingress (disinfectants) that may lead to technical fault alarms. Multiple technical faults in a short time may force ventilators into Safety…

    FDA · DeviceHamilton Medical AGUS nationwide distribution including Puerto Rico.Official notice →
  3. US
    Drugs & medicalClass I

    Intera Oncology, Inc. recalls INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.

    Higher than expected flow rate.

    FDA · DeviceIntera Oncology, Inc.US distribution to states of: AL, CA, IL, KY, MN, MO, NC, NJ, NY, OH, OR, PA,…Official notice →
  4. US
    Drugs & medicalClass II

    Midlab Incorporated recalls Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern…

    CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.

    FDA · DrugMidlab IncorporatedNaionwide within the United StatesOfficial notice →
  5. US
  6. 2022-08-24
  7. US
    Drugs & medicalClass III

    Siemens Medical Solutions USA, Inc recalls AXIOM Sensis or Sensis Vibe Combo systems as follows: System Material # AXIOM Sensis, Combo 64 6623974; AXIOM Sensis, Hemo…

    The Sensis Signal Input Box provides hooks as a milled item on the bottom of the box support the possibility of mounting the Signal Input Box on an accessory rail (e.g., at the patient table), In the event the mounting…

    FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide Distribution Foreign: Albania Algeria Angola Argentina Armenia…Official notice →
  8. US
    Drugs & medicalClass II

    Micro Therapeutics, Inc. recalls Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only

    Outer carton packaging of microcatheters were exposed to wet substance during transport.

    FDA · DeviceMicro Therapeutics, Inc.US Nationwide Distribution: None OUS: BrazilOfficial notice →
See all drugs & medical recalls →