Drugs & medical

Nationwide Pharmaceutical Recalls Iron Dietary Supplements Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

The recalled dietary supplements contain iron which must be in child-resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child-resistant, posing a risk of…

Read the official notice → Ferrous Sulfate (Iron) Enteric-Coated Tablets, 324 mg - 100 Tablet Bottles
Date
2023-06-22
Country
United States
Brand
Prodigy Innovation LLC, of Princeton, New Jersey
Product
Ferrous Sulfate (Iron) Enteric-Coated Tablets, 324 mg - 100 Tablet Bottles
Units
About 4,000
Category
Drugs & medical
Source
CPSC

Copied automatically from the US Consumer Product Safety Commission. Details may be shortened or out of date; the official notice is the authoritative source.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 Consumer Product Safety Commission has the exact models, batch codes and remedy, and it takes priority.

Other drugs & medical recalls in the United States

  1. 2023-06-28
  2. US
    Drugs & medicalClass I

    Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls ICD-DR DDBB2D1 EVERA XT IS1/DF1 INTL, Model Number DDBB2D1; Implantable Cardioverter Defibrillators

    There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators…

    FDA · DeviceMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)US Nationwide - Worldwide DistributionOfficial notice →
  3. US
    Drugs & medicalClass I

    The Harvard Drug Group LLC dba Major Pharmaceuticals and… recalls ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg, Unit Dose Carton 40 Capsules, Rx only, Mfd. By: Dr. Reddy's…

    Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone Hydrochloride Capsules, 20 mg were found to contain blister packages labeled as and containing Dronabinol Capsules, USP, 2.5 mg.

    FDA · DrugThe Harvard Drug Group LLC dba Major Pharmaceuticals and…Nationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass III

    Aurolife Pharma, LLC recalls Glycopyrrolate Tablets, USP, 1 mg, 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC…

    Failed Impurities/Degradation Specifications

    FDA · DrugAurolife Pharma, LLCNationwide within the United StatesOfficial notice →
  5. 2023-06-21
  6. US
    Drugs & medicalClass III

    American Contract Systems, Inc. recalls Total Knee Pack, REF CETJ130, medical convenience kits

    Incorrect expiration date on product.

    FDA · DeviceAmerican Contract Systems, Inc.US Distribution to the state of: MAOfficial notice →
  7. US
    Drugs & medicalClass II

    Boston Scientific Neuromodulation Corporation recalls Driver Instrument, part of the Superion Indirect Decompression System, REF: 102-9800, used with the Superion…

    Pending update to indirect decompression system instructions for use informing users that excessive force during the implant procedure may cause driver instrument tip breaks, which may result in metal fragments (Driver…

    FDA · DeviceBoston Scientific Neuromodulation CorporationUS Nationwide Distribution: IN, NY, IL, PA, FL, SC, TX, MA, VA, AL, WI, OK,…Official notice →
  8. US
    Drugs & medicalClass II

    LumiraDx recalls SteriPack Sterile Polyester Spun Swabs (25 units/Pack)- Intended for sample collection in the intended nasal area. Catalog Number: 60566RevB

    Fails Post-Sterilization Sterile Swabs Cantilever (Bend) Testing and may be more susceptible to breakage. If the swab breaks in the nasal cavity of a patient may cause injury or medical intervention to remove part of…

    FDA · DeviceLumiraDxUS Nationwide distribution.Official notice →
See all drugs & medical recalls →