Drugs & medicalClass II

Amgen, Inc. recalls Sensipar (cinacalcet) Tablets, 60mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA…

CGMP Deviations

Read the official notice →
Date
2026-07-01
Country
United States
Brand
Amgen
Product
Sensipar (cinacalcet) Tablets, 60mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA…
Classification
Class II
Units
Nationwide within the United States
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Amgen recalls

  1. 2026-07-01
  2. US
  3. 2025-03-26
  4. US
    Drugs & medicalClass II

    Amgen, Inc. recalls Neupogen (filgrastim) For Injection, 300mcg/1 mL, 1 mL Single Dose Vials, Rx Only, For Subcutaneous or Intravenous Use Only, Sterile…

    Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.

    FDA · DrugAmgen, Inc.Nationwide in the U.S.A. and Belgium/Luxembourg, Brazil, Chile, Colombia,…Official notice →
  5. 2022-05-18
  6. US
    Drugs & medicalClass II

    Amgen, Inc. recalls MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 ml, Single dose vial, Rx only, Manufactured by…

    Defective container: loose crimp defect, potential loss of container integrity.

    FDA · DrugAmgen, Inc.Nationwide in the USA, Egypt and Lithuania.Official notice →
All 4 Amgen recalls →

Other drugs & medical recalls in the United States

  1. 2026-07-01
  2. US
    Drugs & medicalClass II

    Central Admixture Pharmacy Services, Inc. recalls Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Rx# 24-1269856-0-1Compound…

    Incorrect product formulation: bag did not contain copper and famotidine per label.

    FDA · DrugCentral Admixture Pharmacy Services, Inc.MAOfficial notice →
  3. US
    Drugs & medicalClass II

    Direct Rx recalls DULOXETINE D/R, a) 30 mg (NDC 61919-482-30), 30 Caps; b) 30 mg (NDC 61919-482-60), 60 Caps; CYMBALTA, Packaged and Distributed by Direct Rx.

    CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

    FDA · DrugDirect RxU.S. NationwideOfficial notice →
  4. US
  5. US
  6. US
  7. 2026-06-24
  8. US
    Drugs & medicalClass II

    Thoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog Number: 106531US Software Version: N/A Product…

    Due to 11 volt Backup Battery failures.

    FDA · DeviceThoratec LLCWorldwide - US Nationwide distribution including in the states of AL, AR, AZ,…Official notice →
See all drugs & medical recalls →