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.

Read the official notice →
Date
2023-11-15
Country
United States
Brand
Family Dollar Stores
Product
MEDIC's CHOICE CONTACT LENS SOLUTION 12FLOZ, SKU 998935
Classification
Class II
Units
Distributed to Family Dollar stores in the following states: GA, AL, MS, FL,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Family Dollar Stores recalls

  1. 2023-05-10
  2. 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 →
  3. 2022-09-07
  4. 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 →
  5. 2022-08-31
  6. US
    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.

    FDA · DrugFamily Dollar Stores, Llc.Nationwide within the United StatesOfficial 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. 2023-11-15
  2. US
    Drugs & medicalClass II

    Philips Ultrasound, Inc. recalls Philips Affiniti 70, Diagnostic Ultrasound System Model # 795210

    Their is the potential that diagnostic ultrasound systems operating with software version 10.0 may present a delayed image instead of a real time image.

    FDA · DevicePhilips Ultrasound, Inc.US: AZ, CA, CT, FL, GA, ID, IL, KY, MD, MT, NE, NV, OH, TN, TX, UT, VA OUS:…Official notice →
  3. US
    Drugs & medicalClass II

    Encore Medical, LP recalls RSP Humeral Socket Insert Size 36mm Semi-Constrained +4 mm, REF: 509-01-436, orthopedic shoulder implant component.

    Two different humeral socket Insert devices were swapped during packaging, which could result in surgeons not having the correct device for surgery, which could cause a delay in surgery.

    FDA · DeviceEncore Medical, LPUS: MN, TX, IN, OH, SC, RI, ME, NJ, NY, KS, LA, FL, CAOfficial notice →
  4. US
    Drugs & medicalClass II

    Philips North America Llc recalls DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export digital radiographic images.

    Potential for units suspended on the ceiling to fail and fall.

    FDA · DevicePhilips North America LlcNationwide distribution.Official notice →
  5. US
    Drugs & medicalClass II

    Alcon Research, LLC recalls Alcon Custom-Pak, Surgical Procedure Pack REF 14057-09, 45K W/DUOVISC CATARACT, N VIRGINIA EYE SURG CTR

    Custom surgical procedure packs contain latex gloves but are labeled as "latex free".

    FDA · DeviceAlcon Research, LLCUS: VA OUS: NoneOfficial notice →
  6. US
    Drugs & medicalClass II

    Percussionaire Corporation recalls Monitron II Waveform Analyzer, REF: S00015-1, used with ventilators.

    Note this recall occurred in 2020 and 2021. Reports of screen freeze on visual displays of waveform analyzers that are paired with ventilators. Subsequently, waveform analyzers were serviced to install PAL…

    FDA · DevicePercussionaire CorporationUS: CA, ND, MS, MDOfficial notice →
  7. US
    Drugs & medicalClass II

    Encore Medical, LP recalls DJO EMPOWR Knee Punch Handle, REF: 801-05-040

    Knee punch handle tip is breaking during surgery due to the lack of heat treatment, which may lead to a disruption in surgery.

    FDA · DeviceEncore Medical, LPUS: VA, TN, MN, TX, IL, IN, KY, OH, SC, MS, RI, ME, NJ, NY, MD, CA, KS, LA,…Official notice →
See all drugs & medical recalls →