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.

Read the official notice →
Date
2022-08-24
Country
United States
Brand
Family Dollar Stores
Product
KY JELLY LUBRICANT 2 FL OZ, SKU 901443
Classification
Class II
Units
Product distributed to Family Dollar retail stores in US nationwide.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2023-11-15
  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. 2022-08-31
  8. 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 →
  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. 2022-08-24
  2. US
    Drugs & medicalClass II

    Becton Dickinson & Company recalls BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanically prohibits the…

    Incorrect expiration date listed on the product labels. The expiration date listed on the product label is beyond the expiration date of the product.

    FDA · DeviceBecton Dickinson & CompanyUS Nationwide Distribution CA FL GA IL MD MI OR PA PR TN TXOfficial notice →
  3. US
    Drugs & medicalClass II

    Stradis Medical, LLC dba Stradis Healthcare recalls NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5"; Part Number: ZZ-0700

    The sterile barrier may be compromised.

    FDA · DeviceStradis Medical, LLC dba Stradis HealthcareUS Nationwide distribution in the state of SC.Official notice →
  4. US
    Drugs & medicalClass II

    Trinity Sterile, Inc. recalls Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708

    Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy

    FDA · DeviceTrinity Sterile, Inc.US Nationwide distribution in the states of FL, PA.Official notice →
  5. US
    Drugs & medicalClass II

    Luminex Corporation recalls ARIES SARS-CoV-2 Assay

    SARS-CoV-2 assay that detects SARS-CoV-2 ORF1ab and N genes may not detect the ORF1ab gene. A positive results if either SARS-CoV-2 genes is detected, but If both genes are mistakenly not detected, a false negative…

    FDA · DeviceLuminex CorporationU.S. Nationwide distribution in the states of NE, TX, MS, TN, KY, ME, CA.Official notice →
  6. US
    Drugs & medicalClass II

    Myolyn Inc. recalls Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.

    Screws mounting an internal power supply may come loose during shipping resulting in increased risk of high voltage electrical shock.

    FDA · DeviceMyolyn Inc.Distribution was made to AZ, CA, CT, FL, GA, ID, IL, KY, MA, MI, MN, MO, MN,…Official notice →
  7. US
    Drugs & medicalClass II

    Abbott Molecular, Inc. recalls The Alinity m System, REF 08N53-002, For In Vitro Diagnostic Use.

    Incorrect optical calibration

    FDA · DeviceAbbott Molecular, Inc.There was only foreign distribution to Italy.Official notice →
See all drugs & medical recalls →