SUN PHARMACEUTICAL INDUSTRIES INC recalls Esomeprazole Magnesium Delayed-Release Capsules, USP 20mg, Rx Only, 90 Capsules per bottle, Manufactured by: Ohm Laboratories…
Superpotent Drug: Out of specification for assay at the 12-month timepoint.
Read the official notice →- Date
- 2022-10-05
- Country
- United States
- Brand
- Sun Pharmaceutical Industries
- Product
- Esomeprazole Magnesium Delayed-Release Capsules, USP 20mg, Rx Only, 90 Capsules per bottle, Manufactured by: Ohm Laboratories Inc. New…
- Classification
- Class III
- Units
- Nationwide in the 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- 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 Sun Pharmaceutical Industries recalls
- 2022-12-28
US- 2022-11-30
- US
- 2022-11-09
- US
- 2022-08-03
- US
SUN PHARMACEUTICAL INDUSTRIES INC recalls Divalproex Sodium Delayed-Release Tablets, USP 500mg, Rx Only, 100 Tablets, Distributed by: Sun Pharmaceutical Industries,…
Failed Dissolution Specifications: Failure occurred during routine stability testing of dissolution test.
- 2022-07-20
- US
- 2022-07-13
- US
SUN PHARMACEUTICAL INDUSTRIES INC recalls Testosterone Cypionate Injection, USP, 200mg/ml, Rx Only, One Single-dose vial, Distributed by: Sun Pharmaceutical Industries…
CGMP Deviations: Manufacturing deviations were reported due to an abnormal appearance on parts of machinery.
Other drugs & medical recalls in the United States
- 2022-10-05
- US
QuVa Pharma, Inc. recalls oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride, Injection for IV Use, High Alert, This is a Compounded Product for…
Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of 0.45% Sodium Chloride (500mL) instead of 0.9% Sodium Chloride (500mL).
- US
Novartis Pharmaceuticals Corporation recalls Neoral soft gelatin capsules (cyclosporine capsules, USP) Modified, 25 mg, Rx Only, 30 Soft Gelatin Capsules per carton,…
CGMP deviations: Out of specification results obtained during routine stability testing for ethanol content.
- US
Viatris Inc recalls Ampicillin for Injection, USP, 2 grams/vial NDC 67457-352-02, packaged in 10 x 2 g vials per carton NDC 67457-352-10, Rx only, Mylan…
Presence of Particulate Matter: A complaint was received for the presence of a single strand of hair in one vial.
- 2022-09-28
- US
Paragon 28, Inc. recalls Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture Anchor System
Suture anchor may break upon insertion, which could lead to potential debris in patient, and delays in surgery.
FDA · DeviceParagon 28, Inc.US Nationwide distribution in the states of AZ, IN, LA, NJ, TX, WA, NY, MD,…Official notice → - US
Covidien Llc recalls Puritan Bennett 560 Ventilator, PB560, CFN 4096600
Medtronic has confirmed six reports from customers outside the US where the ventilator became inoperable due to loss of gas supply caused by manufacturing error of specific turbine components.
FDA · DeviceCovidien LlcDomestic distribution to one customer in Washington, D.C. Foreign distribution…Official notice → - US
Associates of Cape Cod, Inc. recalls Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum Ref: FT007
Incorrect information on the Fungitell STAT clamshells containing the Fungitell STAT Standard, relates to printed information for reconstitution and pretreatment volumes
FDA · DeviceAssociates of Cape Cod, Inc.Worldwide distribution - US Nationwide distribution in the state of CA and the…Official notice →