Drugs & medicalClass II

Micro Labs Limited recalls Clobazam Tablets 10mg, 100-count bottle, Rx Only, Manufactured by: Micro Labs Limited Goa-403 722, India. Manufactured for: Micro Labs…

CGMP Deviations: Out of specification for residual solvents.

Read the official notice →
Date
2024-02-28
Country
United States
Brand
Micro Labs
Product
Clobazam Tablets 10mg, 100-count bottle, Rx Only, Manufactured by: Micro Labs Limited Goa-403 722, India. Manufactured for: Micro Labs…
Classification
Class II
Units
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Micro Labs recalls

  1. 2026-08-05
  2. US
    Drugs & medicalClass II

    MICRO LABS USA INC recalls Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0.5%, 10mL - bottle, Rx only, Manufactured by: Micro Labs Limited, India,…

    Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.

    FDA · DrugMICRO LABS USA INCNationwide in the USA.Official notice →
  3. 2024-03-20
  4. US
    Drugs & medicalClass II

    Micro Labs Limited recalls Telmisartan Tablets, USP 40mg, Rx Only, 30 Tablets per bottle, Manufactured by: Micro Labs Limited Goa-403 722, INDIA, Manufactured for:…

    Failed Stability Specifications: Out of specification for blend uniformity.

    FDA · DrugMicro Labs LimitedPuerto Rico, TN, RIOfficial notice →
All 3 Micro Labs recalls →

Other drugs & medical recalls in the United States

  1. 2024-02-28
  2. US
    Drugs & medicalClass I

    Windstone Medical Packaging, Inc. recalls Aligned Medical Solutions, In House Ocular Pack, AMS12947, STERILEEO

    Sterility assurance for saline included in surgical kits cannot be guaranteed.

    FDA · DeviceWindstone Medical Packaging, Inc.US: FL, IL, CA OUS: NoneOfficial notice →
  3. US
    Drugs & medicalClass I

    Cardinal Health 200, LLC recalls Dover" IRRIGATION 1200 CC TRAY, 60 CC PISTON SYRINGE, STERILE SALINE, TIP PROTECTOR, ALCOHOL, LIDDED

    Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.

    FDA · DeviceCardinal Health 200, LLCUS and EMEA, Japan, Latin AmericaOfficial notice →
  4. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Baxter Exactamix Pro 1200, REF EXM12DY

    An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant ingredient delivery of the…

    FDA · DeviceBaxter Healthcare CorporationUS: AL, AZ, CA, FL, GA, IA, KY, MD, MI, MN, MO, NC, NE, NH, NJ, NV, NY, OR,…Official notice →
  5. US
    Drugs & medicalClass II

    MCKESSON CORPORATION recalls CABTREO (clindamycin phosphate, adapalene and benzoyl peroxide) Topical Gel 1.2%/0.15%/3.1%, Not for Oral, Ophthalmic or Intravaginal Use,…

    CGMP Deviations: Product was stored outside labeled storage temperature requirements. Product was exposed to controlled room temperature environment instead of remaining refrigerated.

    FDA · DrugMCKESSON CORPORATIONNationwide in the USOfficial notice →
  6. US
    Drugs & medicalClass I

    Insight Pharmaceuticals LLC, a Prestige Consumer… recalls TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid, NET WT 4.5 oz. (128 g) cans, Distributed by:…

    Chemical Contamination; presence of benzene.

    FDA · DrugInsight Pharmaceuticals LLC, a Prestige Consumer…Product was distributed nationwide and to 4 foreign accounts. Guaynabo, Puerto…Official notice →
  7. US
    Drugs & medicalClass I

    Today The World recalls Arize Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Natural Herbal Remedies, LLC, Cheyenne, WY 82001,…

    Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared nortadalafil, an ingredient found in FDA approved product for the treatment of male sexual enhancement, making this…

    FDA · DrugToday The WorldProduct distributed nationwide within the United States.Official notice →
See all drugs & medical recalls →