Recall Atlas
Drugs & medicalClass II

ARG Laboratories, Inc. recalls ALOE GATOR, (Octocrylene 8%, Octyl Methoxycinnamate 6%, Benzophone 3 6%, Octyl Salicylate 5%), Original Formula, SPF 40+, Broad Spectrum…

Out of Specification for active ingredient

Read the official notice →
Date
2024-06-05
Country
United States
Brand
ARG Laboratories
Product
ALOE GATOR, (Octocrylene 8%, Octyl Methoxycinnamate 6%, Benzophone 3 6%, Octyl Salicylate 5%), Original Formula, SPF 40+, Broad Spectrum…
Classification
Class II
Units
Distributed Nationwide in the USA
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 Details may be shortened or out of date; the official notice is the authoritative source.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 ARG Laboratories recalls

  1. 2024-06-05
  2. US
    Drugs & medicalClass II

    ARG Laboratories, Inc. recalls Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM,…

    Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

    FDA · DrugARG Laboratories, Inc.Distributed Nationwide in the USAOfficial notice →
All 2 ARG Laboratories recalls →

Other drugs & medical recalls in the United States

  1. 2024-06-05
  2. US
    Drugs & medicalClass I

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline Sub-G Endotracheal Tube with Subglottic Suctioning: (1) REF DYNJ18860, Polyurethane Cuff 6.0 mm ID; (2) REF…

    Complaints have been received that the device inflation tube detached and/or tore from the main tube, resulting in potential moisture buildup, loss of pressure, or inability to inflate. There were also reports the…

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldDistribution was nationwide. There was government/military distributon.…Official notice →
  3. US
    Drugs & medicalClass II

    Regeneron Pharmaceuticals Inc recalls EYLEA, (aflibercept) Injection, For Intravitreal injection, 2 mg (0.05mL of a 40mg/mL solution), Single-dose Pre-filled Glass…

    Lack of Assurance of Sterility: Complaints of syringe breakage

    FDA · DrugRegeneron Pharmaceuticals IncUSA nationwide.Official notice →
  4. US
    Drugs & medicalClass II

    ARG Laboratories, Inc. recalls Pain Wizard, Natural Relief for Muscular & Arthritic Pain, (Camphor 3%, Menthol 3%), Enriched with Capsaicin, Camphor, Menthol & MSM,…

    Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

    FDA · DrugARG Laboratories, Inc.Distributed Nationwide in the USAOfficial notice →
  5. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Cefdinir for Oral Suspension USP, 250 mg/5 mL, packaged in a 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.,…

    Defective container: lack of seal integrity.

    FDA · DrugLupin Pharmaceuticals Inc.USA NationwideOfficial notice →
  6. US
    Drugs & medicalClass II

    Rubicon Research Private Limited recalls Metoprolol Tartrate Tablets USP, 25mg, 1000 count bottle, Rx only, distributed by: TruPharma, LLC, Tampa, FL 33609,…

    Presence of Foreign Substance: metal in tablet

    FDA · DrugRubicon Research Private LimitedNationwideOfficial notice →
  7. US
    Drugs & medicalClass II

    Imprimis NJOF, LLC recalls Dexamethasone-Moxifloxacin- Ketorolac (1mg/mL, 0.5 mg/mL and 0.4 mg/mL), Preservative-Free, 1mL Single-Use vials for Intraocular…

    Lack of Assurance of Sterility

    FDA · DrugImprimis NJOF, LLCNationwide within the United StatesOfficial notice →
See all drugs & medical recalls →