2013 Amlodipine recall: Approx. In each case, a recalled drug was contaminated with N-nitrosodimethylamine (NDMA), N-nitrosodiethylamine (NDEA) or N-Nitroso N-Methyl 4 … 10 mg/ 10 mg Amlodipine Besylate, Atorvastatin Calcium tablets, 30-count and 90-count bottles. Reason: CGMP Deviations. The affected businesses for the nine major recalls are Lupin, Mylan, Dr. Reddy’s, Wockhardt, American Health Packaging, Novartis, and Walmart. It’s sold under the brand name Norvasc. 10 mg Amlodipine Besylate tablets, USP, 90 tablets per bottle. While you’re looking into Amlodipine recall data, consider looking into your medical waste disposal spending too. Asked By: Miledys Frere | Last Updated: 19th January, 2020. Manufacturer: InvaGen Pharmaceuticals, Inc. Reason: Incorrect declared strength on label. The FDA are recalling all lots of valsartan produced by Teva Pharmaceuticals, Solco Healthcare,and Major Pharmaceuticals. Find all the resources to help manage your account on our Customer Portal or contact our dedicated customer advocate team directly at 866-924-9339. 62,000 bottles, Mylan Pharmaceuticals. For example, a 2014 Amlodipine recall from Aidapak Services involved 180 tablets. However, not all lots of these medications are affected and being recalled. 10 mg Amlodipine Besylate tablets, USP, 90-count and 500-count bottles. This recall … Disclosure: the images on this page are for illustration only and don’t necessarily reflect recalled products. 173,000 bottles, Dr. Reddy’s Laboratories. 5 mg Amlodipine Besylate tablets in 25-count, 30-count, 100-count, and 300-count cartons. 2013 Amlodipine recall: Approx. NDEA and NDMA are industrial contaminants and both are on lists of … That said, there are four other recalls in the 150,000+ range. 2013 Amlodipine recall: Approx. To see just how much you could save, check out this handy savings calculator. 55,000 bottles, Lupin Pharmaceuticals. Serious side effects of Amlodipine may include irregular heartbeat, increased chest pain, and swelling in the ankles or feet. 10 mg/ 320 mg /25 mg Exforge HCT (Amlodipine, Valsartan, Hydrochlorothiazide), 7 tablets per bottle. Feb 21, 2011. Reason: One lot contained oversized tablets. 2.5 mg Amlodipine Besylate tablets, USP, 90-count bottles. We study 37,043 people who take Amlodipine besylate or have Radiation recall syndrome. Manufacturer: Health Innovations Pharmacy, Inc. 2.5 mg/ 10 mg Amlodipine Besylate, Atorvastatin Calcium tablets, 30-count bottles. Recent FDA Alert(s) for amlodipine Warfarin Sodium Tablets (Jantoven), 3mg: Recall - Mislabeled Bottles Containing Higher Dosage. have risen 18% in the past nine months. 2013 Amlodipine recall: Approx. High blood pressure often has no symptoms. 2.5 mg Amlodipine Besylate tablets, USP, 90-count and 500-count bottles. 4.9/5 (27 Views . For the latest FDA MedWatch alerts, go here. A medical practice or clinic can never recall money wasted on overpriced waste disposal. Lot # DM12975, DM12976, DM12977, DM12986, DM13259, DM13269, DM13270, DM13275, DM13339, DM13341, DM13369, DM13370, DN10088, DN10099, DN10939, DN10940, DM11423, DM11424, DM11425, DM12634, DM12635, DM12660, DM12661, DM12662, DM12663, DM12673, DM12674, DM12684, DM12685, DM12985, DM13162, DM13163, DM13195, DM13196, DM13222, DM13223, DM13271, DM13272, DM13273, DM13274, DM13281, DM13282, DM13296, DM13297, DM13393, DM13394, DM13395, DM13403, DM13404, DM13415, DM13429, DN10077, DN10078, DN10079, DN10080, DN10081, DN10100, DN10104, DN10105, DN10336, DN10342, DN10343, DN10344, DN10355, DN10356, DN10811, DN10812, DN10830, DN10874, DN10875, DN10876, DN10890, DN10891, DN10938, DN10956. 5 mg/ 160 mg/ 12.5 mg Exforge HCT (Amlodipine, Valsartan, Hydrochlorothiazide), 7 tablets per bottle. Blood pressure medicines losartan, valsartan, amlopidine, irbesartan, hydrochlorothiazide, and more hypertension drugs are under FDA recall. The details of the falsely labelled product are: Product Name: Amlodipine 5mg and 10mg tablets. No immediate danger from FDA violations. MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. No immediate danger from FDA violations. Audience: Pharmacy, Family Practice, Consumer, [UPDATED 02/21/2011] Expansion of Recall: Affected Products Include Amantadine, Amlodipine, Androxy, Baclofen, Bethanechol, Jantoven and Oxybutynin. 2015 Amlodipine recall: Several lots, Dr. Reddy’s Laboratories. 10 mg Amlodipine Besylate tablets USP, 1,000-count bottles. Minor recall firms are Health Innovations Pharmacy, Attix, Qualitest, Zydus, Daiichi Sankyo, Aidapak, and Legacy. 23,000 bottles, American Health Pharmacy. Category: medical health heart and cardiovascular diseases. This includes some combination tablets which contain valsartan and amlodipine or valsartan, amlodipine, and hydrochlorothiazide. Below, we’ve listed all 49 Amlodipine recalls to date, along with reasons, lot numbers, dates, manufacturers, and numbers of bottles involved. Why are these medications being recalled? Consumers and pharmacists can call the Upsher-Smith medical information line at 1-888-650-3789 for more information and to access product details, Monday-Friday between 8:00 a.m. and 5:00 p.m. (CST). Teva Pharmaceuticals has initiated a voluntary recall in the United States, to the patient level, of all lots of Amlodipine / Valsartan combination tablets and Amlodipine / Valsartan / Hydrochlorothiazide combination tablets (see table below) due to an impurity detected above specification limits in an active pharmaceutical ingredient (API) manufactured by Mylan India. 2.5 mg/ 10 mg Amlodipine Besylate, Benazepril HCl capsules, 100-count bottles. Lot # 3038339, 3043618, 3041862, 3044258, 2120031, 2120067, 3035787, 3035834, 3035835, 3037125, 3037126, 3037127, 3037511, 3037512, 3037513, 3038113, 3038114, 3038115, 3038116, 3039641, 3039642, 3039643, 3039974, 3040567, 3040977, 3041253, 3041800, 3041801, 3042446, 3042624, 3043015, 3043401, 3043466, 3044590, 09/14 3044591, 3045063, 3045064. In addition, the 3mg tablet is imprinted with the letters WRF, a line, and the number 3 below the line. 10 mg Amlodipine Besylate tablets in 25-count, 100-count, and 300-count cartons. Lot # F0048A, F0056A, F0084, F0085, F0059A, F0088, F0086, F0087, F0061A, F0063W1, F0070A, F0082A. To see if your medication has been affected, check the FDA’s list of recalled products . 2015 Amlodipine recall: Approx. Product Name: Batch Numbers: Manufacturing Date: … Reason: CGMP Deviations. Subscribe to Drugs.com newsletters for the latest medication news, new drug approvals, alerts and updates. 5 mg/ 10 mg Amlodipine Besylate, Atorvastatin Calcium tablets, 30-count and 90-count bottles. The list above simplifies the nine major Amlodipine recalls as of 6/26/17, with 49 recalls total. 10 mg/ 40 mg Amlodipine, Olmesartan Medoxomil (Azor) tablets, 30-count bottles. No report of Radiation recall syndrome is found in people who take Amlodipine besylate. 10 mg/ 40 mg Amlodipine Besylate, Atorvastatin Calcium tablets, 90-count bottle. Audience: Pharmacy, Family Practice, Consumer [UPDATED 02/21/2011] Expansion of Recall: Affected Products Include Amantadine, Amlodipine, Androxy, Baclofen, Bethanechol, Jantoven and Oxybutynin Urgent, with immediate danger of death or serious injury. 2015 Amlodipine recall: Approx. 5 mg/ 10 mg Amlodipine Besylate, Benazepril HCl capsules, 100-count and 500-count bottles. The first bullet point for each recall is its original issue date. © 2020 All Rights Reserved MEDPRO Disposal, LLC, 1751 W Diehl Rd Suite 400, Naperville, IL 60563, United States, Full List of Amlodipine Recalls, FDA 2012-2017. of Amlodipine through 2017. It includes multiple recall numbers for each major recall listed above. The impurity … MedPro provides predictable service at predictable rates. The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. None of the Amlodipine recalls shown here are Class I. Non-immediate risk of death or severe injury. Reason: Discoloration. The biggest event from 2016 affected Novartis Pharmaceuticals. 10 mg/ 40 mg Amlodipine Besylate, Atorvastatin Calcium tablets, 30-count and 90-count bottles. With left ventricular hypertrophy and nephropathy in Type 2 diabetic patients it ’ s Laboratories Administration ( FDA,. 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