Recall Atlas
Drugs & medicalClass I

Sandoz Inc recalls Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Manufactured in…

Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled as penicillin G potassium for Injection, USP, 20 million Unit

Read the official notice →
Date
2025-07-09
Country
United States
Brand
Sandoz
Product
Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Manufactured in…
Classification
Class I
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Sandoz recalls

  1. 2026-06-24
  2. US
    Drugs & medicalClass III

    Sandoz Inc recalls Focalin XR (dexmethylphenidate HCl) 5 mg, 30 extended-release capsules per bottle, Rx only, Manufactured by Societal CDMO Gainesville,…

    Labeling: Incorrect or Missing Lot and/or Exp Date

    FDA · DrugSandoz IncU.S. NationwideOfficial notice →
  3. 2025-09-24
  4. US
    Drugs & medicalClass II

    Sandoz Inc recalls Cyclophosphamide Injection 500 mg/5 mL (100 mg/mL), Hazardous Drug, Rx Only, Sterile, 5mL Multiple Dose Vial, Manufactured in Austria by…

    cGMP deviations: Temperature excursion during transportation.

    FDA · DrugSandoz IncNationwide in the USAOfficial notice →
  5. 2025-09-17
  6. US
    Drugs & medicalClass II

    Sandoz Inc recalls Ciprofloxacin 0.3% and Dexamethasone 0.1% Otic Suspension Rx Only, For Use in Ears Only, Manufactured By: Novartis Manufacturing NV,…

    Temperature Abuse

    FDA · DrugSandoz IncProduct was distributed to one consignee in CA.Official notice →
  7. 2025-07-09
  8. US
    Drugs & medicalClass I

    Sandoz Inc recalls Cefazolin for Injection, USP, 1 gram per vial, Sterile, For Intramuscular or Intravenous Use, Rx Only, Manufactured by Sandoz GmbH for…

    Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were found to contain vials labeled as penicillin G potassium for Injection, USP, 20 million Unit. The vials contained Cefozalin

    FDA · DrugSandoz IncNationwide in the USAOfficial notice →
  9. 2022-04-13
  10. US
    Drugs & medicalClass II

    Sandoz, Inc recalls Orphenadrine Citrate Extended-Release Tablets, USP 100 mg, Rx Only, 100 Tablets, Manufactured by Sandoz Inc., Princeton, NJ 08540 NDC…

    CGMP Deviations:Nitrosamine impurity (NMOA) above the acceptable daily limit.

    FDA · DrugSandoz, IncNationwideOfficial notice →
  11. 2021-12-08
  12. US
    Drugs & medicalClass I

    Sandoz Inc recalls Enoxaparin Sodium Injection, USP, 40 mg/0.4 mL, Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Rx Only;…

    Temperature Abuse; temperature excursion during shipping

    FDA · DrugSandoz IncNationwide in the USOfficial notice →
All 7 Sandoz recalls →

Other drugs & medical recalls in the United States

  1. 2025-07-09
  2. US
    Drugs & medicalClass I

    Philips Respironics, Inc. recalls BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients. BiPAP…

    This device does not indicate for use in patients with respiratory failure.

    FDA · DevicePhilips Respironics, Inc.Worldwide distribution: US (Nationwide)including Guam and Puerto Rico; OUS…Official notice →
  3. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls interventional fluoroscopic x-ray system

    In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high…

    FDA · DeviceSiemens Medical Solutions USA, IncWorldwide.Official notice →
  4. US
    Drugs & medicalClass I

    Maquet Critical Care AB recalls Servo-u Ventilator System. Model Number: 6688600.

    Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

    FDA · DeviceMaquet Critical Care ABUS Nationwide distribution and Puerto Rico. No international distribution.Official notice →
  5. US
    Drugs & medicalClass I

    Sandoz Inc recalls Cefazolin for Injection, USP, 1 gram per vial, Sterile, For Intramuscular or Intravenous Use, Rx Only, Manufactured by Sandoz GmbH for…

    Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were found to contain vials labeled as penicillin G potassium for Injection, USP, 20 million Unit. The vials contained Cefozalin

    FDA · DrugSandoz IncNationwide in the USAOfficial notice →
  6. US
    Drugs & medicalClass III

    AvKARE recalls Pitavastatin Tablets, 1 mg, 90 Tablets per bottle, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC: 42291-905-90

    Failed Impurity/Degradation Specifications

    FDA · DrugAvKARENationwide in the USAOfficial notice →
  7. US
    Drugs & medicalClass III

    Orient Pharma Co., Ltd. Yunlin Plant recalls Pitavastatin Tablets, 1 mg, Rx Only, 90 Tablets, Manufactured by: Orient Pharma Co., Ltd., 8 Kehu 1st Road, Huwei Chen,…

    Failed Impurities/Degradation Specifications.

    FDA · DrugOrient Pharma Co., Ltd. Yunlin PlantNJOfficial notice →
See all drugs & medical recalls →