A synthetic Levothyroxine recall in January 2020 in the UK is similar in nature and degree. M328F19-3, expiration date November 2020. Latest News Medications with “use by,” “discard after” or “expiration date” on or after December 2020 are not impacted by the recall. Acella Pharmaceuticals is voluntarily recalling one … All lots with expiry between 10/2020-07/2023 or Lot #: J18C68, exp. 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. These kinds of quality control issues happen now and then to all drug categories, and thyroid pharmaceuticals of all types, not just desiccated thyroid, face them. We've had to deal with several recalls of thyroid medications over the year which has caused a significant amount of stress for those who suddenly had to switch medications or dosages.. Lot numbers are: NP Thyroid 30 mg: Lot M329A19-1 expiration 20-Dec, lot … These 13 people defined the Bay Area in 2020. 42192-328-01, Lot No. October 15, 2020 Kimberly-Clark Announces Recall of Cottonelle Flushable Wipes Sold at: Walmart stores, Walmart.com, Sam's Clubs and SamsClub.com. On August 15 and 16, 2018, WRCB TV reported on a recall of a levothyroxine and liothyronine product manufactured by Westminster Pharmaceuticals. Signs and symptoms of hypothyroidism include constipation, puffy face, slow heart rate, hair loss, increased sensitivity to cold, fatigue, dry skin, swelling of the thyroid gland, depression and/or difficulty losing weight or unexplained weight gain. Medications with “use by,” “discard after” or “expiration date” on or after December 2020 are not impacted by the recall. 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. The pills subject to recall are packed in 100-count bottles. This is the second recall this month related to deficiencies in the active ingredients in drugs used to treat hypothyroidism. The Acella Pharmaceuticals recall is the most recent, but it's far from the only one. The company is … Levothyroxine (T4)/Liothyronine (T3) (NP Thyroid) Tablet Recall Sep 21, 2020 1:00 PM 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. Date – October 2020) and one NP Thyroid® 120 mg (Lot #M328F19-1; Exp. We will … The drug is used to improve symptoms of hypothyroidism like slow speech, lack of energy, weight gain, hair loss and dry skin. Full Story. Patients who are currently taking NP Thyroid from the lots being recalled should not discontinue use without contacting their healthcare provider first for further guidance and/or a replacement prescription. Earlier this month, RLC Labs recalled 483 lots of Nature-Throid and WP Thyroid because tests revealed they "may have as low as 87% of the labeled amount of Liothyronine (T3) or Levothyroxine(T4). If a recall does relate to the ... CLASS I. 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 ET. NP Thyroid® 15, Thyroid Tablets, USP, ¼ grain (15 mg); NDC 42192-327-01; lot no. Another pharmaceutical company has recalled its medication for an underactive thyroid because it may not be strong enough. M327E19-1, expiration date October 2020. Patients should contact their healthcare provider for further guidance and/or a replacement prescription. October 7, 2020 Facebook Share Sep 17, 2020. Symptoms can include "fatigue, increased sensitivity to cold, constipation, dry skin, puffy face, hair loss, slow heart rate, depression, swelling of the thyroid gland and/or unexplained weight gain or difficulty losing weight," the agency said. Then John will discuss the financial results in more detail, including the company's fiscal 2020 financial guidance. Patients who received sub potent levothyroxine (t4) and liothyronine (t3) thyroid tablets, USP may experience signs and symptoms of hypothyroidism (underactive thyroid). The product may have as low as 87% of the labeled amount of levothyroxine (T4). The recall affects 37 unexpired lots of levothyroxine and liothyronine (Thyroid Tablets, USP) 15, 30, 60, 90 and 120 milligrams. "There is reasonable risk of serious injury in newborn infants or pregnant women with hypothyroidism including early miscarriage, fetal hyperthyroidism, and/or impairments to fetal neural and skeletal development," according to the announcement. Earlier this month, another manufacturer called RLC Labs recalled 483 lots of two thyroid medications called WP Thyroid and Nature-Thyroid for sub-potency. However, we incorrectly included an image of another Levothyroxine is one of two active ingredients in the drugs used to treat hypothyroidism, or an underactive thyroid. The company is voluntarily recalling one lot of 15-mg and one lot of 120-mg NP Thyroid, Thyroid Tablets “because testing found these lots to be sub potent. The recall comes after the Florida-based Westminster Pharmaceuticals used ingredients that were found to have deficiencies in conjunction with the FDA’s current good manufacturing practices. Acella has received four reports of "adverse events” for the medication. ... LLC, is recalling Levothyroxine and Liothyronine tablets in 15 mcg, 30 mcg, ... Crock-Pot burns spark recall of nearly 1M units. Audience: Consumer, Health Professional, Pharmacy. ET to 5 p.m. 42192-328-01, Lot No. RLC Labs recalled 483 lots of Nature-Throid and WP Thyroid, NP Thyroid 15, Thyroid Tablets, USP, ¼ grain (15 mg), NDC No. This is interesting as I normally have 50mcg oral solution Levothyroxine and I cannot get it as it’s out of stock. 7 months ago. In June, the Food and Drug Administration (FDA) ruled that several generic levothyroxine preparations had the same clinical effect and … Lots of popular thyroid hormone replacement medication, levothyroxine / liothyronine, were recently recalled due to concerns over contamination. Symptoms of hypothyroidism can return in patients treated for an underactive thyroid who take a subpotent drug, the FDA warned. 2020 Has Been a Rough Year For Thyroid Patients. Westminster Pharmaceuticals, LLC is voluntarily recalling all lots, within expiry, of … Acella Pharmaceuticals announced the voluntary recall of 1 lot of NP ... as low as 87% of the labeled amount of levothyroxine. Newborn infants may develop fetal hyperthyroidism and/or impairments to fetal neural and skeletal developments. ", Sportmix Pet Food Recalled After Deaths of at Least 28 Dogs, Ceiling Fans Sold at Home Depot Recalled After Blades Fly Off, Copyright © 2021 NBCUniversal Media, LLC. All rights reserved. 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 products are being recalled because testing of samples from six lots by the FDA found the samples to be sub-potent. Patients who are currently taking levothyroxine (T4) and liothyronine (T3) thyroid tablets, USP from the lots being recalled should not abruptly stop the medication. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. In euthyroid patients, doses within the range of daily hormonal requirements are ineffective for weight reduction. October 21, 2020 Jakks Pacific Recalls to Repair Morfboard® Skate & Scoot Scooters Due to Fall Hazard Sold at: Walmart stores and Walmart.com. Levothyroxine is taken by more than 13 million Americans to treat an underactive thyroid, thyroid gland enlargement, nodules, or cancer. M328F19-3, expiration date November 2020. THE RECALL: The first official FDA-announced recall was announced May, 2020. Drugs.com provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. NP Thyroid 120, Thyroid Tablets, USP, 2 grain (120 mg), NDC No. 42192-327-01, Lot No. the Food and Drug Administration announced last week. Next, we should put this recall in context of other drug recalls. ... on or after December 2020 are not impacted by this recall. There is reasonable risk of serious injury in special populations with hypothyroidism. "In elderly patients and patients with underlying cardiac disease toxic cardiac manifestations of hyperthyroidism may occur, such as cardiac pain, palpitations or cardiac arrhythmia.". The other active ingredient is liothyronine. The recalled products were distributed nationwide and packed in 100-count bottles: According to the announcement, Acella has “received four reports of adverse events” for the medication. The recall affects 13 lots of 30-mg, 60-mg, and 90-mg tablets, which came in 100-count bottles. Consumers with questions about the recall can email Acella Pharmaceuticals at recall@acellapharma.com or call 1-888-280-2044 Monday through Friday from 8:00 a.m. Click here to read the FDA’s full recall … 2020 has been a rough year for everyone but especially for thyroid patients! Manufactured by: RLCLabs or Packaged by: PD-Rx Pharmaceuticals Incorporated. Find Recalls from December 2020 on ConsumerAffairs. This story was reported from Cincinnati. 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. The FDA said Acella is proactively notifying its wholesalers to discontinue distribution of the recalled products. The product may have as low as 87% of the labeled amount of levothyroxine.". I can’t find it at the moment, but the Acella website stated this recall was about NP made in late 2018. Here’s what you need to know about the recall. 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. This blog post is meant to keep you up to date with all three of the major … Risk in pregnant women include early miscarriage. Our list of Recalls includes automotive, appliance, food, technology, clothing, and more. 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 recalled 120 mg tablet has lot number M328F19-3, an expiration date of November 2020 and NDC number of 42192-328-01. So I requested 100mcg oral solution and I had the same reply also out of … It referred to super potency for the 30mg, 60mg and 90mg tablets. Elderly patients may experience cardiac pain, palpitations, or cardiac arrhythmia. Updated Sep 09, 2020; Posted Sep 09, 2020 RLC Labs, Inc. is voluntarily recalling a total of 483 lots of Nature-Throid and WP Thyroid because they may be subpotent. Thyroid hormones, including Levothyroxine sodium tablets, USP, either alone or with other therapeutic agents, should not be used for the treatment of obesity or for weight loss. (CBS) — There is a recall out for certain thyroid medications because they may not be strong enough to be effective. M327E19-1; expiration date Oct. 2020. NP Thyroid Recall by Acella. NP Thyroid 120, Thyroid Tablets, USP, 2 grain (120 mg), NDC No. The affected lots include one NP Thyroid® 15 mg (Lot #M327E19-1; Exp. Date – November 2020). 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. In May 2020, Acella Pharmaceuticals recalled 13 lots of NP Thyroid tablets due to super-potency. Acella Pharmaceuticals is recalling two lots of its thyroid medication after testing found they may not be strong enough, the Food and Drug Administration announced last week. 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