Recall Atlas
Drugs & medicalClass I

Botanical Be recalls Artri King Reforzado con Origa y Omega 3 tablets, packaged in 100-count bottles, Manufactured by: Plantas medicinales de Mexico, Melchol…

Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.

Read the official notice →
Date
2023-12-06
Country
United States
Brand
Botanical Be
Product
Artri King Reforzado con Origa y Omega 3 tablets, packaged in 100-count bottles, Manufactured by: Plantas medicinales de Mexico, Melchol…
Classification
Class I
Units
USA 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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2023-12-06
  2. US
    Drugs & medicalClass II

    Breas Medical, Inc. recalls with Notch 22M/15F sold as part of Breas Medical MPV circuit 2 pc Kits: 006093, 006653, an accessory to ventilator device, Vivo 45LS.…

    Produced with unintended open slits on the side of the mouthpiece body, may result in insufficient ventilation in spontaneous breathing patients using MPV-VCV and MPV-PCV modes of ventilation

    FDA · DeviceBreas Medical, Inc.Nationwide Foreign: CanadaOfficial notice →
  3. US
    Drugs & medicalClass II

    PATH recalls SENTIERO SCREENING, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S

    Affected lots of product may experience technical distortions to a greater extent than expected.

    FDA · DevicePATHUS States: FL, MO, OH, WIOfficial notice →
  4. US
    Drugs & medicalClass II

    Becton Dickinson Infusion Therapy Systems Inc. recalls BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Technology 20GA X 1.00in, REF: 382533

    Over-the-needle, intravascular catheters may have needles that do not retract properly into the barrel, which could result in contaminated needlestick injury, blood leaking from the insertion site or catheter, and…

    FDA · DeviceBecton Dickinson Infusion Therapy Systems Inc.US Nationwide distribution in the states of CA, NC, MI, WA, CO, FL, NJ, NM,…Official notice →
  5. US
    Drugs & medicalClass I

    Bayer Healthcare Pharmaceuticals Inc. recalls VITRAKVI (larotractenib) oral solution, 20mg/mL, 100 mL bottle, Rx only, Manufactured for Bayer HealthCare Pharmaceuticals…

    Microbial Contamination of Non-Sterile Products: microbial contamination identified as Penicillium brevicompactum observed during routine ongoing stability testing

    FDA · DrugBayer Healthcare Pharmaceuticals Inc.Product was distributed to specialty pharmacies and distributors nationwide…Official notice →
  6. US
    Drugs & medicalClass II

    Golden State Medical Supply Inc. recalls PAROXETINE tablets, USP, 10 mg, Packaged as a) 30-count bottle, NDC 60429-734-30; b) 90-count bottle NDC 60429-734-90;…

    Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine

    FDA · DrugGolden State Medical Supply Inc.Nationwide in the USAOfficial notice →
  7. US
    Drugs & medicalClass III

    Teva Pharmaceuticals USA, Inc recalls Testosterone Gel, 1.62% CIII (Alcohol 80% v/v), packaged in 30 unit-dose packets per carton, Rx only, Teva Pharmaceuticals USA,…

    OOS for viscosity

    FDA · DrugTeva Pharmaceuticals USA, IncUSA nationwideOfficial notice →
See all drugs & medical recalls →