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Recall Details. Drug Recall Enforcement Report Class II voluntary initiated by Trigen Laboratories, originally initiated on 06-17-2024 for the product Methylphenidate Hydrochloride, Extended-release Tablets, USP, 36mg, 100-count Bottle, Rx Only, Manufactured for: Trigen Laboratories, LLC, Alpharetta, GA 30005, NDC 13811-708-10 The product was ...
10 sty 2020 · On Wednesday, the Food and Drug Administration announced voluntary recalls of prescription forms of ranitidine by two generic drug companies, Appco Pharma and Northwind Pharmaceuticals, bringing...
Pharmascience Inc. is recalling 30 lots of over-the-counter ranitidine drugs (150 mg tablets), packaged in blister packs, after tests found NDMA, a nitrosamine impurity, above the acceptable level in some lots.
11 paź 2024 · The Drug Enforcement Reports included in this listing was last updated on October 11, 2024 and include a total of 16455 recall reports. Recall Number Recall Initiation Date
Recalls, Market Withdrawals, & Safety Alerts. The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products. Not all...
Some ARBs have been recalled due to the presence of, or potential for, nitrosamine impurities. Products not on this list have not been recalled in Canada. Recalls taking place in other countries may not affect Canadian products.
30 sty 2021 · Pharmascience Inc. is recalling 23 additional lots of its over-the-counter ranitidine drugs (75 mg tablets) after tests found NDMA, a nitrosamine impurity, above accepted levels.
