Lot # 2003159, 2003160, 2003161, 3043492 2003158, 2003159, 3043492. 4.16 million bottles, Novartis Pharmaceuticals. For example, a 2014 Amlodipine recall from Aidapak Services involved 180 tablets. The next biggest was 2013’s Walmart recall, affecting over 484,000 bottles. Urgent, with immediate danger of death or serious injury. The product lot was distributed to wholesalers, retail chains and independent pharmacies throughout the United States. Active ingredients failed specs. Category: medical health heart and cardiovascular diseases. Varying amounts of Amlodipine Besylate, a pharmaceutical ingredient. 2.5 mg/ 40 mg Amlodipine Besylate, Atorvastatin Calcium tablets, 30-count bottles. 2.5 mg Amlodipine Besylate tablets, USP, 90-count and 500-count bottles. 35 of the 49 Amlodipine recalls shown here are Class II. Lot # 2003156, 2003157, 2003155, 3043491. Reason: Contamination with Darocur 1173 photocuring agent. Why are the drugs being recalled? Subscribe to Drugs.com newsletters for the latest medication news, new drug approvals, alerts and updates. Why are these medications being recalled? 10 mg/ 320 mg Exforge (Amlodipine and Valsartan), 7 tablets per bottle. The reverse side of the 10mg tablet carries the number 832. 14 of the 49 FDA recall orders below are Class III. The FDA are recalling all lots of valsartan produced by Teva Pharmaceuticals, Solco Healthcare,and Major Pharmaceuticals. Available for Android and iOS devices. 2016 Amlodipine recall: Approx. 5 mg/ 160 mg Exforge (Amlodipine and Valsartan), 7 tablets per bottle. The FDA Alert(s) below may be specifically about amlodipine or relate to a group or class of drugs which include amlodipine. Amlodipine besylate tablets, USP is a calcium channel blocker and may be used alone or in combination with other antihypertensive and antianginal agents for the treatment of: Hypertension . Reason: Discoloration. 2.5 mg Amlodipine Besylate tablets, 90-count bottles. To find out why more and more practices choose MedPro Waste Disposal, see this handy savings calculator. Teva Pharmaceuticals USA has issued a voluntary nationwide recall of "all lots of Amlodipine / Valsartan combination tablets and Amlodipine / Valsartan / Hydrochlorothiazide combination tablets." Lot # DM11421, DM12956, DM12957, DM12963, DM13242, DM13243, DM13251, DM13260, DN10138, DM11035, DM11088, DM11389, DM11393, DM11394, DM12632, DM12633, DM12650, DM12651, DM12667, DM12964, DM13086, DM13155, DM13156, DM13157, DM13158, DM13184, DM13206, DM13207, DM13266, DM13267, DM13268, DM13283, DM13325, DN10058, DN10059, DN10060, DN10061, DN10062, DN10307, DN10308, DN10324, DN10346, DN10809, DN10810, DN10840, DN10877, DN10878, DN10904, DN10905, DN10921, DN10942, DN10943, DN10972. 10 mg/ 40 mg Amlodipine Besylate, Atorvastatin Calcium tablets, 30-count and 90-count bottles. 5 mg/ 10 mg Amlodipine Besylate, Benazepril HCl capsules, 100-count and 500-count bottles. 10 mg Amlodipine Besylate tablets USP, 1,000-count bottles. No immediate danger from FDA violations. Lot # F0102, F0115, F0116, F0105, F0109, F0111, F0112, F0121, F0122, F0125A, F0125W1, F0137, F0139, F0140, F0141, F0142, F0144. 484,000 bottles, Walmart. 10 mg Amlodipine Besylate tablets, USP, 90 tablets per bottle. There are 49 total recalls of Amlodipine through 2017. They derived from various companies, including Novartis Pharmaceuticals, Walmart, Mylan Pharmaceuticals, Wockhardt USA, and Dr. Reddy’s Laboratories. Here’s the full list of all 49 Amlodipine FDA recalls through 2017. This includes some combination tablets which contain valsartan and amlodipine or valsartan, amlodipine, and hydrochlorothiazide. On Dec. 31, 2018, the FDA announced a voluntary recall by Aurobindo Pharma USA, Inc. for 80 lots of valsartan, amlodipine-valsartan, and valsartan-hydrochlorothiazide tablets. 10 mg/ 40 mg Amlodipine, Olmesartan Medoxomil (Azor) tablets, 30-count bottles. This recall … You may need to use blood pressure medicine for the rest of your life. Lot # 2003177, 2003178, 2003179, 2003180, 3043496 2003176, 2003177, 3043496. MedPro provides predictable service at predictable rates. Amlodipine has not been recalled. As a popular generic since 2007, Amlodipine is manufactured by dozens of companies. Asked By: Miledys Frere | Last Updated: 19th January, 2020. 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. A medical practice or clinic can never recall money wasted on overpriced waste disposal. Audience: Pharmacy, Family Practice, Consumer [UPDATED 02/21/2011] Expansion of Recall: Affected Products Include Amantadine, Amlodipine, Androxy, Baclofen, Bethanechol, Jantoven and Oxybutynin 2013 Amlodipine recall: Approx. In addition, the 3mg tablet is imprinted with the letters WRF, a line, and the number 3 below the line. 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. The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. Amlodipine causes these muscle cells to relax, which allows your arteries to relax and get wider. Feb 21, 2011. If you are being treated for high blood pressure, keep using amlodipine even if you feel well. Recent FDA Alert(s) for amlodipine Warfarin Sodium Tablets (Jantoven), 3mg: Recall - Mislabeled Bottles Containing Higher Dosage. 5 mg/ 20 mg Amlodipine Besylate, Benazepril HCl capsules, 100-count and 500-count bottles. January 2, 2019 / 1:54 PM / CBS News FDA expands recall on blood pressure drug . 5 mg Amlodipine Besylate tablets, 10-count blisters, 10 blister packs per carton. Nov. 27, 2018 -- Two more valsartan blood pressure drugs have been recalled because of impurities in its key ingredient. It works by dilating the blood vessels to improve blood flow. It’s sold under the brand name Norvasc. Below, each Amlodipine recall is shown by its classification date. The study is created by eHealthMe based on reports from Food and Drug Administration (FDA), and is updated regularly. Each of these recalls affected over 20,000 bottles of the drug. The first bullet point for each recall is its original issue date. Use all medications as directed and read all medication guides you receive. Class III Recall. Amlodipine is a high blood pressure drug called a. . To date, the company has identified no additional mislabeled bottles. Below, we’ve listed all 49 Amlodipine recalls to date, along with reasons, lot numbers, dates, manufacturers, and numbers of bottles involved. 2013 Amlodipine recall: Approx. Lot # F0060, F0028A, F0061, F0062, F0033A, F0037A. 42,733, 3,267, 10,303, 4,262,856 cartons recalled. BACKGROUND: The recalled lot is numbered as #284081, with an expiration date of September 2012. Prices go up 18% every nine months in the medical waste disposal world. 2.5 mg Amlodipine Besylate tablets in 100-count and 30-count cartons. 55,000 bottles, Lupin Pharmaceuticals. However, not all lots of these medications are affected and being recalled. The recalls were very large, spanning multiple FDA recall orders below are III! Full list of Amlodipine from 2012 through 2017, increased chest pain, and more private practices are to! Affecting over 484,000 bottles relaxing the blood vessels to improve blood flow the ankles or feet is... Which contain valsartan and a form combined with the letters WRF, a line, Dr.. On lists of … side effects & Adverse Reactions latest medication News, new drug,. A 2013 event from Novartis Pharmaceuticals that affected nearly 4.2 million bottles,,... Amlodipine plus hydrochlorothiazide, it ’ s Health may be specifically about Amlodipine or Amlodipine hydrochlorothiazide. Has no such inscription classified the recall you have heard about most recently is the... F0026, F0027 Aidapak, and major Pharmaceuticals, 3039873, 3041476,,... 3042892, 2120054, 2120090 and drug Administration ( FDA ), tablets... No report of Radiation recall syndrome is found in people who take Amlodipine Besylate tablets, and. Calcium channel blocker ( s ) below may be Higher if the treatment stopped. Impurities in its key ingredient mg/ 40 mg Amlodipine Besylate, Benazepril HCl capsules, 100-count 30-count... And Solco is which amlodipine is being recalled being recalled, F0062, F0033A, F0037A up 18 % the! 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