Teva Pharmaceuticals USA recalls Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules, USP) 120 mg, Rx Only, 90 capsules, labelled as (a) Manufactured By: Teva…
Labelling: Incorrect Exp. Date
Read the official notice →- Date
- 2021-11-24
- Country
- United States
- Brand
- Teva Pharmaceuticals
- Product
- Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules, USP) 120 mg, Rx Only, 90 capsules, labelled as (a) Manufactured By: Teva…
- Classification
- Class II
- Units
- Distributed 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Teva Pharmaceuticals recalls
- 2022-02-09
USTeva Pharmaceuticals USA recalls Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10 mg/10 mg, 100-count bottle, Rx Only, Manufactured by:…
Failed Dissolution Specification: Dissolution results are below specification limits for the active ingredient
- 2022-01-26
- US
Teva Pharmaceuticals USA recalls Brinzolamide Ophthalmic Suspension, USP 1%, packaged as a)10 ml dropper bottles (NDC 0591-2127-79), and b) 15 ml dropper bottles (NDC…
Defective Container: The notch in the cap that fits into the nozzle of the dropper could break off and block the dropper possibly resulting in the product not dispensing.
- 2022-01-19
- US
Teva Pharmaceuticals USA recalls MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL), 10 mL Multiple-Dose Vial, Rx Only, Manufactured for:…
Lack of Assurance of Sterility
FDA · DrugTeva Pharmaceuticals USAMethylprednisolone, TN Norepinephrine BItartrate - MS, OHOfficial notice → - 2021-12-29
- US
- 2021-11-24
- US
Teva Pharmaceuticals USA recalls Clonidine Transdermal System, USP 0.1 mg/day, 4 patches per carton, Rx only, Manufactured by: Actavis Laboratories, UT Inc., Salt Lake…
Failed Impurities/Degradation Specifications
- 2021-10-27
- US
Teva Pharmaceuticals USA recalls AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC…
Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Other drugs & medical recalls in the United States
- 2021-11-24
- US
Bayer Healthcare Pharmaceuticals Inc. recalls Tinactin (Tolnaftate 1%) DEODORANT POWDER SPRAY NET WT 133g (4.6 OZ) can, labeled as (a) UPC 3 11017-410-00 4, NDC…
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
FDA · DrugBayer Healthcare Pharmaceuticals Inc.Distributed Nationwide in the US, Puerto Rico, Canada and Mexico through a…Official notice → - US
Teva Pharmaceuticals USA recalls Clonidine Transdermal System, USP 0.1 mg/day, 4 patches per carton, Rx only, Manufactured by: Actavis Laboratories, UT Inc., Salt Lake…
Failed Impurities/Degradation Specifications
- US
Amneal Pharmaceuticals of New York, LLC recalls Flocinolone Acetonide 0.01% Topical Oil, Body Oil, Rx, packaged in 4 oz. bottle, Distributed by: Amneal Pharmaceuticals…
Subpotent Drug: Out-of-specification assay result was obtained for Fluocinolone Acetonide.
FDA · DrugAmneal Pharmaceuticals of New York, LLCProduct was distributed nationwide within the United StatesOfficial notice → - 2021-11-17
- US
Baxter Healthcare Corporation recalls Hemodialysis Delivery System, Software Version 2.x.
If the operator initiates therapy with a saved prescription profile and makes a change to the prescription after a disposable filter change using the Same Patient button, the system may suggest values from the original…
FDA · DeviceBaxter Healthcare CorporationDistributed nationwide to AL, AR, AZ, CA, CO, CT, FL, GA, HI, ID, IL, IN, KY,…Official notice → - US
BioCheck, Inc. recalls T4 EIA Kit, Cat No: BC-1007, Store at 2-8C, For in vitro diagnostic use only This product s intended use is For the quantitative…
Immunoassay TEST Kit do not meet product shelf-life standards resulting in failed controls.
FDA · DeviceBioCheck, Inc.US Distribution to states of: MI, FL, NJ, OH, CA; and OUS (foreign)…Official notice → - US
Philips North America Llc recalls Philips Azurion Interventional Fluoroscopic X-Ray System, Software version 2.1.x, Model numbers 722063, 722064, 722067, 722068, 722078,…
When the user presses or releases both the APC (accept) button and the Float Tabletop (panning) button at the same time, the geometry may stop reacting on movement requests (table lock-up) and X-ray imaging becomes…
FDA · DevicePhilips North America LlcDomestic distribution nationwide. International distribution worldwide.Official notice →