Drugs & medicalClass II

Lupin Pharmaceuticals Inc. recalls Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202…

Failed Dissolution Specifications

Read the official notice →
Date
2023-12-20
Country
United States
Brand
Lupin Pharmaceuticals
Product
Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202…
Classification
Class II
Units
Product was distributed to 3 wholesale/distributor accounts.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Lupin Pharmaceuticals recalls

  1. 2024-02-07
  2. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Rifampin Capsules USP 150mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United…

    Subpotent Drug and Failed Impurities/Degradation Specifications

    FDA · DrugLupin Pharmaceuticals Inc.Product was distributed to 32 Wholesale/distributor accounts who further…Official notice →
  3. US
    Drugs & medicalClass II

    Lupin Pharmaceuticals Inc. recalls Cefixime for Oral Suspension 100mg/5mL, 50 mL bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland…

    Failed Impurities/Degradation Specifications

    FDA · DrugLupin Pharmaceuticals Inc.Nationwide in the USAOfficial notice →
  4. 2024-01-17
  5. 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 →
  6. 2023-08-09
  7. US
    Drugs & medicalClass I

    Lupin Pharmaceuticals Inc. recalls Tydemy (drospirenone, ethinyl estradiol and levomefolate calcium tablets, 3 mg/0.03 mg/0.451 mg and levomefolate calcium tablets 0.451…

    Failed Stability Specification and Failed Impurities/Degradation Specifications: out of specification for inactive content ascorbic acid and MTHFRC-7impurity test

    FDA · DrugLupin Pharmaceuticals Inc.USA nationwide.Official notice →
  8. 2023-07-19
  9. US
    Drugs & medicalClass III

    Lupin Pharmaceuticals Inc. recalls Amlodipine Besylate Tablets, USP 10 mg, 1000-count bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland…

    Subpotent Drug: Out-of-Specification test results observed in assay test at 21-month long term stability study.

    FDA · DrugLupin Pharmaceuticals Inc.Product was distributed directly to three distributors in TN and NJ. Product…Official notice →
  10. 2023-02-01
  11. US
    Drugs & medicalClass III

    Lupin Pharmaceuticals Inc. recalls Clobetasol propionate Cream USP, 0.05%, 45 g tube, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202,…

    Subpotent Drug: Low assay result observed during long-term stability testing.

    FDA · DrugLupin Pharmaceuticals Inc.USA NationwideOfficial notice →
All 38 Lupin Pharmaceuticals recalls →

Other drugs & medical recalls in the United States

  1. 2023-12-20
  2. US
    Drugs & medicalClass I

    Philips North America Llc recalls Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR) systems are Medical…

    Firm was informed of an event in which the structural integrity of the MR system components failed due to unintended excessive pressure buildup of helium gas during a magnet quench. If the system is unable to contain…

    FDA · DevicePhilips North America LlcDomestic distribution to AL AZ CA CO DE FL GA IA IL IN KS KY LA MA MD MI MO NE…Official notice →
  3. US
  4. US
  5. 2023-12-13
  6. US
    Drugs & medicalClass II

    Ortho-Clinical Diagnostics, INc. recalls VITROS Chemistry Products ECO2 Slides-For in vitro diagnostic use only. VITROS Chemistry Products ECO2 Slides quantitatively…

    Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing that some lots from Coating 3598 of VITROS ECO2 slides included carts which may contain consecutive slides that may not function as intended.…

    FDA · DeviceOrtho-Clinical Diagnostics, INc.Nationwide Foreign: Bermuda CanadaOfficial notice →
  7. US
    Drugs & medicalClass II

    Encore Medical, LP recalls DJO surgical EMPOWR Porous Knee System Empowr 3D Femur-Porous Coated SIZE 8 Left 3D MATRIX COATED REF 243-01-108 DJO surgical EMPOWR…

    Due to incorrect product/device within packaging.

    FDA · DeviceEncore Medical, LPUS Nationwide distribution.Official notice →
  8. US
    Drugs & medicalClass II

    Fresenius Medical Care Holdings, Inc. recalls Stay Safe Cap

    Updating the labeling to include additional warnings and contraindications for potential side effects.

    FDA · DeviceFresenius Medical Care Holdings, Inc.US Nationwide distribution.Official notice →
See all drugs & medical recalls →