Recall Atlas
Drugs & medicalClass II

McKesson Corporation dba McKesson Drug Company recalls Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL bottle, Rx only, Manufactured by: Teligent…

CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.

Read the official notice →
Date
2022-05-11
Country
United States
Brand
McKesson Corporation dba McKesson Drug Company
Product
Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL bottle, Rx only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310…
Classification
Class II
Units
Nationwide in the United States including Guam and the Northern Mariana Islands.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2022-05-11
  2. US
    Drugs & medicalClass I

    Best Brands Consumer Products, Inc. recalls Mickey Mouse Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./to mL bottle, Best Brands Consumer Products, Inc., c/o Best Brands…

    Chemical Contamination; FDA analysis found product to contain methanol

    FDA · DrugBest Brands Consumer Products, Inc.Nationwide in the USOfficial notice →
  3. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Lansoprazole Delayed-Release Orally Disintegrating Tablets, 30 mg, 10 Packs of 10 Tablets each, 100 Tablets per blister pack, Rx…

    Failed Dissolution Specifications

    FDA · DrugDr. Reddy's Laboratories, Inc.OHOfficial notice →
  4. US
    Drugs & medicalClass II

    Torrent Pharma Inc recalls Pantoprazole Sodium Delayed-Release Tablets, USP, 20 mg, Rx Only, 90 tablets per bottle, Manufactured by: Torrent Pharmaceuticals Ltd.,…

    CGMP deviations: tablets cracking

    FDA · DrugTorrent Pharma IncNationwide in the U.S.AOfficial notice →
  5. US
    Drugs & medicalClass III

    Akorn, Inc. recalls Lidocaine Hydrochloride Oral Topical Solution, USP (Viscous) 2%, 100 mL per bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co., Inc.…

    Failed viscosity specification - product was below specificcation

    FDA · DrugAkorn, Inc.Nationwide USA and Puerto RicoOfficial notice →
  6. US
    Drugs & medicalClass II

    Viatris Inc recalls alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0068-1.

    Failed Dissolution Specifications: low out-of-specification dissolution test results observed.

    FDA · DrugViatris IncProduct was distributed nationwide in the USAOfficial notice →
  7. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Losartan Potassium Tablets USP, 100 mg, a) 90-count bottles (NDC# 68180-378-03), b) 1000-count bottles (NDC# 68180-378-09), Rx Only,…

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

    FDA · DrugLupin Pharmaceuticals Inc.Product was distributed nationwideOfficial notice →
See all drugs & medical recalls →