Recall Atlas
Drugs & medicalClass III

Siegfried Barbera, SL recalls Votrient (pazopanib) 200 mg tablets, 120-count bottle, Rx Only, Manufactured by: Siegried Barbera, S.L., Barbera del Valles, Spain,…

Failed Dissolution Specifications

Read the official notice →
Date
2023-12-20
Country
United States
Brand
Siegfried Barbera, SL
Product
Votrient (pazopanib) 200 mg tablets, 120-count bottle, Rx Only, Manufactured by: Siegried Barbera, S.L., Barbera del Valles, Spain,…
Classification
Class III
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2023-12-20
  2. US
    Drugs & medicalClass II

    Spectranetics Corporation recalls Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX REF 420-159 Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 OTW…

    Incorrect product labeling. Exterior product box label does not match internal pouch label.

    FDA · DeviceSpectranetics CorporationU.S Nationwide - Worldwide Distribution: US Distribution: AL, AR, AZ, CA, CO,…Official notice →
  3. US
    Drugs & medicalClass I

    Philips North America Llc recalls Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR) systems are Medical…

    Firm was informed of an event in which the structural integrity of the MR system components failed due to unintended excessive pressure buildup of helium gas during a magnet quench. If the system is unable to contain…

    FDA · DevicePhilips North America LlcDomestic distribution to AL AZ CA CO DE FL GA IA IL IN KS KY LA MA MD MI MO NE…Official notice →
  4. US
    Drugs & medicalClass II

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Liothyronine Sodium Tablets, USP 5 mcg, 100-count bottle, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc.…

    Failed Impurities/Degradation Specifications

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCNationwideOfficial notice →
  5. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202…

    Failed Dissolution Specifications

    FDA · DrugLupin Pharmaceuticals Inc.Product was distributed to 3 wholesale/distributor accounts.Official notice →
  6. 2023-12-13
  7. US
    Drugs & medicalClass II

    Ortho-Clinical Diagnostics, INc. recalls VITROS Chemistry Products ECO2 Slides-For in vitro diagnostic use only. VITROS Chemistry Products ECO2 Slides quantitatively…

    Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing that some lots from Coating 3598 of VITROS ECO2 slides included carts which may contain consecutive slides that may not function as intended.…

    FDA · DeviceOrtho-Clinical Diagnostics, INc.Nationwide Foreign: Bermuda CanadaOfficial notice →
  8. US
    Drugs & medicalClass II

    Encore Medical, LP recalls DJO surgical EMPOWR Porous Knee System Empowr 3D Femur-Porous Coated SIZE 8 Left 3D MATRIX COATED REF 243-01-108 DJO surgical EMPOWR…

    Due to incorrect product/device within packaging.

    FDA · DeviceEncore Medical, LPUS Nationwide distribution.Official notice →
See all drugs & medical recalls →