Drugs & medicalClass III

American Health Packaging recalls Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals), 100 mg, 100 Capsules (10 x 10), 10-count blisters per card, 10 cards per…

Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to dissolution failure at 0-time of the repackaged lot. Drug release results were above specification at 0-time.

Read the official notice →
Date
2022-05-25
Country
United States
Brand
American Health Packaging
Product
Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals), 100 mg, 100 Capsules (10 x 10), 10-count blisters per card, 10 cards per carton,…
Classification
Class III
Units
Nationwide 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 Details may be shortened or out of date; the official notice is the authoritative source.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 American Health Packaging recalls

  1. 2026-09-09
  2. US
  3. 2022-05-04
  4. US
  5. 2022-03-16
  6. US
    Drugs & medicalClass II

    American Health Packaging recalls Oxycodone Hydrochloride Oral Solution, USP (C-II), 5 mg/5 mL, Delivers 5 mL per Cup, 1 Tray of 10 Cups, Rx Only, For Institutional Use…

    Impurity failure at 0-time of the repackaged lot.

    FDA · DrugAmerican Health PackagingNationwide in the USAOfficial notice →
  7. 2022-02-02
  8. US
  9. 2021-10-27
  10. US
    Drugs & medicalClass II

    American Health Packaging recalls GlipiZIDE Extended-Release Tablets, 2.5 mg, 30 Tablets (3 blister cards each with 10 individually blistered doses), Rx only,…

    Failed Dissolution Specifications: results were above specification.

    FDA · DrugAmerican Health PackagingNationwide within the USAOfficial notice →
  11. 2021-10-06
  12. US
    Drugs & medicalClass II

    American Health Packaging recalls Valproic Acid Oral Solution, USP, 500 mg/10 mL, 100 10 mL unit dose cups per case, Rx Only, Packaged and Distributed by: American…

    CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.

    FDA · DrugAmerican Health PackagingNationwide USAOfficial notice →
All 7 American Health Packaging recalls →

Other drugs & medical recalls in the United States

  1. 2022-05-25
  2. US
    Drugs & medicalClass I

    Avanos Medical, Inc. recalls Avanos Cortrak 2 Enteral Access System (EAS)

    Product labeling is being modified. STOP using the Anonymous Account Mode feature of the CORTRAK 2 device immediately. CONFIRM placement of the NG/NI tube per institution protocol.

    FDA · DeviceAvanos Medical, Inc.Worldwide Distribution. US Nationwide, Australia, Austria, Canada, Germany,…Official notice →
  3. US
    Drugs & medicalClass II

    Cardinal Health Inc. recalls Trulicity (dulaglutide) injection, 0.75 mg/0.5mL once weekly, 4 Single-Dose Pens, Rx only, Eli Lilly and Company, Indianapolis, IN 46285,…

    TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions

    FDA · DrugCardinal Health Inc.NM onlyOfficial notice →
  4. US
    Drugs & medicalClass III

    Apotex Corp. recalls Sirolimus Oral Solution, 1 mg/mL, 60 mL bottle, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for:…

    Failed Dissolution Specifications: Sirolimus Oral Solution recalled due to lot RZ1598 exceeded the specification limit at the 14-month timepoint.

    FDA · DrugApotex Corp.Nationwide in the USAOfficial notice →
  5. US
    Drugs & medicalClass III

    Bestco LLC recalls Open Nature Cough Drops Menthol-Cough Suppressant/Oral Anesthetic Peppermint Naturally Flavored, packaged in Bags of 30 lozenges,…

    Subpotent drug: Low OOS for menthol content at the three month room temperature.

    FDA · DrugBestco LLCCA, ID, PA, OKOfficial notice →
  6. US
    Drugs & medicalClass III

    Monarch PCM, LLC recalls Phenobarbital Elixir, USP 20 mg/5 mL, 1 Pint (473 mL) bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC Tampa, FL…

    Does Not Meet USP or OTC Monograph: Product exceeds USP specification for alcohol content

    FDA · DrugMonarch PCM, LLCTN onlyOfficial notice →
  7. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls GaviLyte -C (Polyethylene Glycol 3350, 240 g) and electrolytes for Oral Solution, USP with flavor pack NDC# 43386-060-19

    Failed Stability Specification

    FDA · DrugLupin Pharmaceuticals Inc.Product was distributed nationwide, including Puerto Rico.Official notice →
See all drugs & medical recalls →