Recall of NP Thyroid Tablets
On October 28, 2020, the U.S. Food and Drug Administration (FDA) announced that Acella Pharmaceuticals, LLC is voluntarily recalling two lots of NP Thyroid Tablets, 15mg and 120mg as a Class I Recall.
Only some lots are being recalled because testing has found them to contain a lower percentage of an ingredient than what is listed on the label. The product may have as low as 87% of the ingredient Levothyroxine (T4).
Please note that not all lots are affected so you may not be affected by this recall. Your health and safety are important to us. If you are currently taking NP Thyroid Tablets, 15mg, and/or 120mg that are made by Acella Pharmaceuticals, please contact your health care provider to discuss which other treatments or medicines may be appropriate.
For more information, please visit https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/acella-pharmaceuticals-llc-issues-voluntary-nationwide-recall-two-lots-np-thyroidr-thyroid-tablets. You can also contact Acella Pharmaceuticals, LLC by phone at 1-888-280-2044 (TTY 711), Monday through Friday, 8 a.m. to 5 p.m., ET or by email at recall@acellapharma.com. In addition, you can call the Horizon NJ Health Pharmacy Help Desk at 1-800-682-9094 x81016 (TTY 711), Monday through Friday, 8 a.m. to 6 p.m., and Saturday 8 a.m. to 4:30 p.m., ET.