Recall Atlas
Drugs & medicalClass I

Stop Clopez Corp recalls Schwinnng Herbal Dietary Supplement Capsules, packaged in 10-count boxes, distributed by VSD Productions Inc., Las Vegas, NV.

Marketed Without An Approved NDA/ANDA

Read the official notice →
Date
2024-05-22
Country
United States
Brand
Stop Clopez Corp
Product
Schwinnng Herbal Dietary Supplement Capsules, packaged in 10-count boxes, distributed by VSD Productions Inc., Las Vegas, NV.
Classification
Class I
Units
Distribution worldwide via amazon.com
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2024-05-22
  2. US
    Drugs & medicalClass II

    MACLEODS PHARMA USA, INC recalls Losartan Potassium and Hydrochlorothiazide Tablets, USP 50mg /12.5 mg, 1000-count bottle, Rx only, Manufactured for: Macleods Pharma…

    Presence of foreign substance: plastic-like substance.

    FDA · DrugMACLEODS PHARMA USA, INCUSA NationwideOfficial notice →
  3. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Cefdinir for Oral Suspension USP 250 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx only, Manufactured for: Lupin…

    Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.

    FDA · DrugLupin Pharmaceuticals Inc.USA nationwideOfficial notice →
  4. US
    Drugs & medicalClass II

    Dercher Enterprises, Inc., DBA Gordon Laboratories recalls Gordofilm Wart Remover (salicylic acid 16.7% USP) packaged in 15 cc glass jars, Gordon Laboratories, Upper…

    cGMP Deviations

    FDA · DrugDercher Enterprises, Inc., DBA Gordon LaboratoriesProduct was distributed nationwide within the United StatesOfficial notice →
  5. 2024-05-15
  6. US
    Drugs & medicalClass III

    Randox Laboratories Ltd. recalls Evidence MultiSTAT with software v 3.7-Analyzer intended for the qualitative determination of parent drug molecule and metabolites of…

    Foam gasket on the Evidence MultiSTAT chip heater assembly may not perform as expected. Foam that is not functioning as expected may cause light to leak into the Charged Coupled Device (CCD) Camera during imaging. This…

    FDA · DeviceRandox Laboratories Ltd.US Nationwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    Stryker Leibinger GmbH & Co. KG recalls Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization and rigid fixation of the bony areas…

    Mislabeled: Product labeled 56-90614 (90x90 Gold Mesh), was actually 56-90314 (90x90 Blue Mesh), may cause a delay in procedure

    FDA · DeviceStryker Leibinger GmbH & Co. KGNationwideOfficial notice →
  8. US
    Drugs & medicalClass II

    NRT X-RAY A/S recalls Intelli-C: Right side suspended Tabletop, REF: 03400000; Left side suspended Tabletop, REF: 03400010, used with the Intelli-C X-ray system

    X-ray system C-arm may experience uncontrolled motion if 1) AC motor controller firmware has a faulty setting, 2) the Motor/gear assembly is worn, 3) CAT movement is driven at maximum speed and angulated more than 75…

    FDA · DeviceNRT X-RAY A/SUS Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, WV,…Official notice →
See all drugs & medical recalls →