Recall Atlas
Drugs & medicalClass I

InvaGen Pharmaceuticals, Inc. recalls Vigabatrin for Oral Solution, USP 500 mg per packet, 50 packets per box, Rx Only, Manufactured by: InvaGen Pharmaceuticals, Inc.,…

Defective Container: powder may leak out of the pouch

Read the official notice →
Date
2024-01-17
Country
United States
Brand
InvaGen Pharmaceuticals, Inc.
Product
Vigabatrin for Oral Solution, USP 500 mg per packet, 50 packets per box, Rx Only, Manufactured by: InvaGen Pharmaceuticals, Inc., (a…
Classification
Class I
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

Other drugs & medical recalls in the United States

  1. 2024-01-17
  2. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Tizanidine Tablets, USP 4mg, 150-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC…

    Presence of Foreign tablets/capsules - identified as tizanidine 2 mg tablets.

    FDA · DrugDr. Reddy's Laboratories, Inc.USA NationwideOfficial notice →
  3. US
    Drugs & medicalClass II

    Rising Pharma Holding, Inc. recalls buPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150mg, 30-count bottles, Rx Only, Manufactured for: Rising Pharma…

    Presence of Foreign Tablets/Capsules

    FDA · DrugRising Pharma Holding, Inc.Nationwide within the United StatesOfficial notice →
  4. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Desloratadine Tablets USP 5mg a) 100 count (NDC 68180-153-01) and b) 500 count (NDC 68180-153-02) bottles, Rx Only, Manufactured for:…

    CGMP Deviations: N-Nitroso Desloratadine impurity result exceeded the acceptable intake limit.

    FDA · DrugLupin Pharmaceuticals Inc.Product was distributed nationwide.Official notice →
  5. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Tacrolimus Capsules, USP 1mg, 100-Count Bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories Limited, Bachupally, 500 090,…

    Presence of Foreign Tablets/Capsules: One 0.5 mg Tacrolimus capsule found in a bottle of 1 mg Tacrolimus capsules.

    FDA · DrugDr. Reddy's Laboratories, Inc.US Nationwide.Official notice →
  6. 2024-01-10
  7. US
    Drugs & medicalClass II

    Zimmer Biomet Spine Inc. recalls Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixation System

    Spinal fixation system 7.5mmx 50mm screws are packaged with the correct labeling, but the screws themselves were laser marked with an incorrect size description of 7.5 x 40; use of incorrect screws could lead to screw…

    FDA · DeviceZimmer Biomet Spine Inc.US Nationwide distribution in the states of MN, NE.Official notice →
  8. US
    Drugs & medicalClass II

    Philips Respironics, Inc. recalls Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B DS2110X11B EE2100X15B…

    The following was missing from the Contraindications Statement: The AVAPS-AE therapy mode is contraindicated for invasive use and patients less than 10 kg. The AVAPS feature is contraindicated for patients less than 10…

    FDA · DevicePhilips Respironics, Inc.Worldwide distribution: US (nationwide)-AK, AL, AR, AZ, CA, CO, CT, DE, FL,…Official notice →
See all drugs & medical recalls →