Levothyroxine is used to treat an underactive thyroid gland (hypothyroidism).It replaces or provides more thyroid hormone, which is normally produced by the thyroid gland. Westminster Pharmaceuticals has recalled the 15, 30, 60, 90, and 120 milligram versions of levothyroxine and liothyronine at wholesale level. On August 15 and 16, 2018, WRCB TV reported on a recall of a levothyroxine and liothyronine product manufactured by Westminster Pharmaceuticals. Thyroid news report: On May 22nd, 2020 Acella Pharmaceuticals issued a voluntary nationwide recall of certain lots of NP thyroid due to superpotency. One of the most popular drugs in the country, levothyroxine also known as the brand name Synthroid is in short supply, making prices higher and even leaving some patients without the drug. The product may have as low as 87% of the labeled amount of levothyroxine … Medicine recalls : The United Kingdom: Class 2 Medicines Recall: Wockhardt UK Ltd, Levothyroxine 100micrograms/5ml Oral Solution : Medicines and Healthcare products Regulatory Agency (MHRA) announces that Wockhardt UK Ltd is recalling 2 batches of Levothyroxine 100micrograms/5ml Oral Solution (batch number: I53481 and I54522) from … MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. Acella LLC is recalling specific lots of 15 mg and 120 mg levothyroxine (T4) and liothyronine (T3) thyroid tablets, USP (NP Thyroid) due to sub potency identified during testing. Acella Pharmaceuticals announced the voluntary recall of 1 lot of NP Thyroid® (levothyroxine and liothyronine) 15mg and 1 lot of NP Thyroid 120mg as … CLASS I. Nature Throid, 1/2 grain (32.5 mg) thyroid USP [liothyronine (T3) 4.5 mcg, levothyroxine (T4) 19 mcg], 3/4 grain (48.75 mg) thyroid USP [liothyronine (T3) 6.75 mcg, levothyroxine (T4) 28.5 … So my pharmacist requested 25mcg oral and to take twice as much. The recall affects 37 unexpired lots of levothyroxine and liothyronine (Thyroid Tablets, USP) 15, 30, 60, 90 and 120 milligrams. Consumers with questions about the recall can email RLC Labs, Inc. at recall@rlclabs.com or contact RLC Labs, Inc. The drug is used to improve symptoms of hypothyroidism like slow speech, lack of energy, weight gain, hair loss and dry skin. September 09, 2020 10:01 AM, ORDER REPRINT → The FDA-posted recall notice written by manufacturer RLC Labs said this “sub potency” is why all … If a recall does relate to the version of the drug you are taking, you should not stop taking the drug until you discuss an alternative treatment with your doctor or pharmacist. The shortage is a result of hurricanes Irma and Maria, which hit Puerto Rico nearly four months ago, and knocked out manufacturing facilities for many drugs and medical supplies, including levothyroxine. The pharmacist who contacted us was responding to a comment from one of our readers. According to an announcement made by the U.S. Food and Drug Administration, the affected drugs are sold under the names NP Thyroid® 15 and NP Thyroid® 120.The former recalled lot has an expiration date of October 2020, a lot number of M42192-327-01, and an NDC (National Drug Code) number of 42192-327-01, while the latter expires on November 2020 with a lot number of M328F19-3, … The recalled 15 mg tablet has lot number M327E19-1, an expiration date of October 2020 and NDC number of 42192-327-01. 10 December 2020. On Sept. 17, 2020, Acella Pharmaceuticals further announced that one lot of 15 mg and one lot of 120 mg NP Thyroid (thyroid tablets, USP) are being recalled because testing has found these lots to be subpotent. This is interesting as I normally have 50mcg oral solution Levothyroxine and I cannot get it as it’s out of stock. Patients who received sub potent levothyroxine (t4) and liothyronine (t3) thyroid tablets, USP may experience signs and symptoms of hypothyroidism (underactive thyroid). NP Thyroid 120, Thyroid Tablets, USP, 2 grain (120 mg), NDC No. To date, Acella has received two reports of adverse events related to this recall. Find Recalls from January 2021 on ConsumerAffairs. September 22, 2020. Questions & Answers. Cancel Post Info. The pills subject to recall are packed in 100-count bottles. RLC Labs, Inc. is voluntarily recalling a total of 483 lots of Nature-Throid® and WP Thyroid® in all strengths, all counts of product within current expiry to the consumer level. Find Recalls from October 2020 on ConsumerAffairs. The Acella Pharmaceuticals recall is the most recent, but it's far from the only one. On August 15 and 16, 2018, WRCB TV reported on a recall of a levothyroxine and liothyronine product manufactured by Westminster Pharmaceuticals. August 26, 2020 So I requested 100mcg oral solution and I had the same reply also out of … The product may have as low as 87 percent of the labeled amount of Liothyronine (T3) or Levothyroxine (T4). The FDA announced a recall of thyroid medicine from Acella Pharmaceuticals, LLC . This recall includes a total of 483 lots of both Naturethroid and WP Thyroid in all strengths and within current expiration on consumer levels. Top Searches Holiday Gifts. Nature-throid and WP Thyroid recall for Subpotency - September 3rd, 2020. Here are some things you need to be aware of. The second recall was a much bigger deal than the first. Levothyroxine Recall. Audience: Consumer, Health Professional, Pharmacy. The pharmacist who contacted us was responding to a comment from one of our readers. Add Info. Thyroid hormones, including Levothyroxine sodium tablets, USP, either alone or with other therapeutic agents, should not be used for the … The Acella Pharmaceuticals recall is the most recent, but it's far from the only one. Acella Pharmaceuticals – Recall of NP Thyroid® (thyroid tablets) • On May 22, 2020, Acella Pharmaceuticals announced a consumer-level recall of thirteen lots of NP Thyroid (thyroid tablets) because testing has found the recalled lots to be superpotent. Find Recalls from October 2020 on ConsumerAffairs. The product may have as low as 87% of the labeled amount of levothyroxine (T4). THE RECALL: On August 25th, 2020, RLC announced the recall of both of their desiccated thyroid products due to sub-potency. September 17, 2020 -- Acella Pharmaceuticals, LLC is voluntarily recalling one lot of 15-mg and one lot of 120-mg NP Thyroid®, Thyroid Tablets, USP [levothyroxine … Another pharmaceutical company has recalled its medication for an underactive thyroid because it may not be strong enough. The FDA has issued a “Voluntary Recall” on Westminster Pharmaceuticals of all lots of their Levothyroxine and Liothyronine (Thyroid Tablets). Click here to read the FDA’s full recall … This is the second recall this month related to deficiencies in the active ingredients in drugs used to treat hypothyroidism Published September 21, 2020 • Updated on September 21, 2020 … Christine Blank. Earlier this month, another manufacturer called RLC Labs recalled 483 lots of two thyroid medications called WP Thyroid and Nature-Thyroid for sub-potency. NP Thyroid Recall by Acella. Patients should contact their healthcare provider for further guidance and/or a replacement prescription. M328F19-3, expiration date November 2020. © 2021 National Community Pharmacists Association, FDA announces voluntary recall of thyroid medication, NCPA Innovation Center/ CPESN Community Pharmacy Fellowship, Nominate yourself or a peer for pharmacy quality awards, Make sure to register for our new learning center, Report COVID-19 vaccine billing issues here, Jump-start the year with an action plan for success, It’s filling up fast: Ownership Workshop is Jan. 30-31. We will then open the … This person was concerned about potential variations between generic formulations of levothyroxine. 1 Lori Loughlin; 2 Croatian Earthquake; 3 Mcconnell Stimulus; 4 Bridgerton; 5 GoDaddy Domains; 6 Cam Newton; 7 Steaks … Two thyroid medications are being voluntarily recalled over concerns about an ingredient in the tablets. Earlier this month, another manufacturer called RLC Labs recalled 483 lots of two thyroid medications called WP Thyroid and Nature-Thyroid for sub-potency. The FDA announced a recall of thyroid medicine from Acella Pharmaceuticals, LLC . Here’s what you need to know about the recall. Get an alert when a recall is issued. Sep 21, 2020 1:00 PM. The product may have as low as 87% of the labeled amount of levothyroxine. Westminster Pharmaceuticals, LLC, is recalling Levothyroxine and Liothyronine tablets in 15 mcg, 30 mcg, 60 mcg, 90 mcg and 120 mcg doses. M327E19-1; expiration date Oct. 2020. M328F19-3, expiration date November 2020. 2 results. NP Thyroid Recall by Acella. We will then open the call for questions. NP Thyroid® 15, Thyroid Tablets, USP, ¼ grain (15 mg); NDC 42192-327-01; lot no. However, we incorrectly included an image of another RLC Labs, Inc. is voluntarily recalling a total of 483 lots of Nature-Throid and WP Thyroid in all strengths, all counts of product, within current expiry to the consumer level. The drug is used to improve symptoms of hypothyroidism like slow speech, lack of energy, weight gain, hair loss and dry skin. Lots of popular thyroid hormone replacement medication, levothyroxine / liothyronine, were recently recalled due to concerns over contamination. The product may have as low as 87% of the labeled amount of levothyroxine (T4). Additional information is available at the following links: 50 N Medical Dr A050Salt Lake City, Utah 84132, Complete a paper form and fax to 1-800-FDA-0178. 42192-328-01, Lot No. Date – November 2020). She had been switched from levothyroxine made by Mylan to levothyroxine from Lannett and then levothyroxine from Sandoz. This all took place in less than six months. 42192-328-01, Lot No. September 16, 2020 Cooper Tire & Rubber Co. Recall Due to Low Tread Gauge May Cause Tire Failure Sold at: Walmart stores, Walmart.com, Sam's Clubs and SamsClub.com. The affected lots include one NP Thyroid® 15 mg (Lot #M327E19-1; Exp. So I requested 100mcg oral solution and I had the same reply also out of stock with no update on next delivery/ availability. The shortage is a result of hurricanes Irma and Maria, which hit Puerto Rico nearly four months ago, and knocked out manufacturing facilities for many drugs and medical supplies, including levothyroxine. See the lot numbers below: NP Thyroid 30 mg: Lot M329A19-1 … The product may have up to 115.0% of the labeled amount of liothyronine (T3). Westminster Pharmaceuticals, LLC is voluntarily recalling all lots, within expiry, of Levothyroxine and Liothyronine (Thyroid Tablets, USP) 15 mg, 30 mg, 60 mg, 90 mg, & 120 mg to the wholesale level. September 9, 2020. Ask a Question. The product may have as low as 87% of the labeled amount of levothyroxine ... (15 mg), NDC No. Newborn infants may develop fetal hyperthyroidism and/or impairments to fetal neural and skeletal developments. Top Searches Holiday Gifts. Thyroid news report: On May 22nd, 2020 Acella Pharmaceuticals issued a voluntary nationwide recall of certain lots of NP thyroid due to superpotency.. Don't worry, I'm going to explain in plain English what this all means and how it applies to you. In other words, the tablets had more than the … There is reasonable risk of serious injury in special populations with hypothyroidism. Cancel Post Message. NCPA Information provided on this site is intended for use only by residents of the United States. They … This person was concerned about potential variations between generic formulations of levothyroxine. Levothyroxine oral tablets (Synthroid) are used to treat hypothyroidism, goiter, and certain types of thyroid cancer. In euthyroid patients, doses within the range of daily hormonal requirements are ineffective for weight reduction. With that said, I will now turn the call over to Tim Crew. We will then open the call for questions. Our list of Recalls includes automotive, appliance, food, technology, clothing, and more. Following is a list of possible medication recalls, market withdrawals, alerts and warnings. 7 months ago. Message. Here’s what you need to know about the recall. Both recalls are due to sub-potency of drugs that treat hypothyroidism. This all took place in less than six months. Acella LLC is recalling specific lots of 15 mg and 120 mg levothyroxine (T4) and liothyronine (T3) thyroid tablets, USP (NP Thyroid) due to sub potency identified during testing. September 16, 2020 MWE Investments Recalls Westinghouse Portable Generators Due to Fire Hazard Sold at: Sam's Clubs and SamsClub.com. Christine Blank. Potential interaction between fluoxetine and levothyroxine. Audience: Endocrinologists and other healthcare professionals. One lot of 15-mg and one lot of 120-mg NP Thyroid tablets, USP [levothyroxine (T4) … NCPA September 9, 2020 The products are being recalled because testing of samples from six lots by the FDA found the samples to be sub-potent. The products are being recalled because testing has found these lots to be sub potent. Elderly patients may experience cardiac pain, palpitations, or cardiac arrhythmia. Click here to read the FDA’s full recall announcement. Then John will discuss the financial results in more detail, including the company's fiscal 2020 financial guidance. Pharmaceuticals Westminster lots, all recalling voluntarily is LLC expiry, within Tablets, (Thyroid Liothyronine and Levothyroxine of mg, 15 USP) mg, 30 mg, 60 mg, 90 wholesale, the to mg 120 & 2020-05 of instead 2023-05 instigator by agreed is date alternative an unless issued date the from month 1 for open remain will recall This be will this of date … Comment. Sep 17, 2020 . Side Effects & Adverse Reactions. In May 2020, Acella Pharmaceuticals recalled 13 lots of NP Thyroid tablets due to super-potency. Best of all, it's free! (Gray News) - The U.S. Food and Drug Administration issued a recall notice for Acella Pharmaceuticals, LLC for two lots of medicine for people with hypothyroidism. The recalled 120 mg tablet has lot … Uses. I have called Wockhardt in Wrexham for an update and they cannot give me a ETA. The product may have as low as 87% of the labeled amount of levothyroxine … Best of all, it's free! Lots of popular thyroid hormone replacement medication, levothyroxine / liothyronine, were recently recalled due to concerns over contamination. (Source: FDA) By Gray News Staff | September 21, 2020 at 11:47 AM EDT - Updated September 21 at 11:49 AM Patients who are currently taking levothyroxine (T4) and liothyronine (T3) thyroid tablets, USP from the lots being recalled should not abruptly stop the medication. Earlier this month, RLC Labs issued a nationwide recall of all lots of its Nature-Throid and WP Thyroid, also due to sub … This recall happened on September 3rd (2) ... For levothyroxine (4), each dose of 100mcg of levothyroxine must be between 96mcg and 104mcg. She had been switched from levothyroxine made by Mylan to levothyroxine from Lannett and then levothyroxine from Sandoz. The pills subject to recall are packed in 100-count bottles. Read the FDA notice here. Acella Pharmaceuticals, LLC Issues Voluntary Nationwide Recall of Two Lots of NP Thyroid® (Thyroid Tablets, USP) Due to Sub Potency. Don't worry, I'm going to explain in plain English what this all means and how it applies to you. FDA and King Pharmaceuticals notified healthcare professionals of revisions to the PRECAUTIONS, ADVERSE REACTIONS and DOSAGE AND ADMINISTRATION sections of labeling, describing reports of choking, gagging, tablets stuck in throat and dysphagia while taking … Finally, and most importantly, the recall statement also claims that an increase in T3 potency alone, of this magnitude, may cause “signs and symptoms of hyperthyroidism (overactive thyroid).” September 17, 2020 -- Acella Pharmaceuticals, LLC is voluntarily recalling one lot of 15-mg and one lot of 120-mg NP Thyroid®, Thyroid Tablets, USP [levothyroxine (T4) and liothyronine (T3)] to the consumer level. 42192-327-01, Lot No. Westminster Pharmaceuticals, LLC, which has its Corporate HQ in Tampa, Florida, is voluntarily recalling all lots, within the expiration date, of Levo-thyroxine and Lio-thyronine (Thyroid Tablets) dosages of 15 mg, 30 mg, 60 mg, 90 mg, & … Then John will discuss the financial results in more detail, including the company's fiscal 2020 financial guidance. In May 2020, Acella Pharmaceuticals recalled 13 lots of NP Thyroid tablets due to super-potency. If you aren't already aware, NP thyroid is a prescription thyroid medication which … Trending. The recall affects 13 lots of 30-mg, 60-mg and 90-mg tablets, which came in 100-count bottles. RECALL ALERT: Two thyroid medications recalled due to contamination concerns Levothyroxine and Liothyronine are being recalled in their tablet … Patients and healthcare providers can report any adverse reaction related to subpotent NP Thyroid® products to the FDA’s MedWatch program in 1 of 2 ways. ATLANTA, Sept. 18, 2020 /PRNewswire/ — Acella Pharmaceuticals, LLC is voluntarily recalling one lot of 15-mg and one lot of 120-mg NP Thyroid ®, Thyroid Tablets, USP [levothyroxine (T4) and liothyronine (T3)] to the consumer level.The products are being recalled because testing has found these lots to be sub potent. 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