Drugs & medicalClass II

Elevate Oral Care recalls Povi-One, 10% Povidone-Iodine Oral Antiseptic, Packaged by Elevate Oral Care, LLC, 346 Pike Road, Suite 6, West Palm Beach, FL 33411, NDC…

sub potency

Read the official notice →
Date
2026-07-01
Country
United States
Brand
Elevate Oral Care
Product
Povi-One, 10% Povidone-Iodine Oral Antiseptic, Packaged by Elevate Oral Care, LLC, 346 Pike Road, Suite 6, West Palm Beach, FL 33411, NDC…
Classification
Class II
Units
Nationwide
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Elevate Oral Care recalls

  1. 2024-09-18
  2. US
    Drugs & medicalClass III

    Elevate Oral Care recalls Just Right 5000, 1.1% Sodium Fluoride, Candy Apple Flavor, Net Wt. 3.4oz (97g), Rx Only, Manufactured for Elevate Oral Care, LLC in the…

    LABELING: LABEL MIX-UP.

    FDA · DrugElevate Oral Care120 direct customers, Nationwide US. No foreign, DOD/VA.Official notice →
All 2 Elevate Oral Care recalls →

Other drugs & medical recalls in the United States

  1. 2026-07-01
  2. US
    Drugs & medicalClass II

    Intuitive Surgical, Inc. recalls Da Vinci ASSY, PSS, SP1098, Part Number: 380601

    Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engagement and may result in uncontrolled…

    FDA · DeviceIntuitive Surgical, Inc.Worldwide - US Nationwide distribution including in the states of CA, GA, OH,…Official notice →
  3. US
    Drugs & medicalClass I

    Medline Industries, LP recalls Medline Convenience Kits: 1) DYNJ905503F, Model Number: CV ANESTHESIA - ROOM SET UP; 2) DYNJ905503G, Model Number: CV ANESTHESIA - ROOM…

    The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified…

    FDA · DeviceMedline Industries, LPUS Nationwide.Official notice →
  4. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Perampanel CIII Tablets, 6mg, Rx only, 30 Tablets, Mfd.by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761,…

    Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwide in the USAOfficial notice →
  5. US
    Drugs & medicalClass II

    Annora Pharma Private Limited recalls Lacosamide Tablets, USP, C V, 100mg, Rx only, 60-count bottle, By: Annora Pharma Pvt., Ltd, Sangareddy -502313, Telangana, India,…

    Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.

    FDA · DrugAnnora Pharma Private LimitedNationwide in the USAOfficial notice →
  6. US
    Drugs & medicalClass I

    CareFusion 213, LLC recalls BD ChloraPrep FREPP Clear,(2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)) 1.5 mL Applicator, 20 Applicators,…

    Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.

    FDA · DrugCareFusion 213, LLCNationwide inthe USA, as well as other foreign distribution.Official notice →
  7. US
    Drugs & medicalClass I

    CareFusion 213, LLC recalls BD ChloraPrep Clear (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)), 1 mL Applicator, 60 Applicators per inner…

    Non-Sterility: Due to presence of Aspergillus penicillioides.

    FDA · DrugCareFusion 213, LLCNationwide inthe USA, as well as other foreign distribution.Official notice →
See all drugs & medical recalls →