2024/2/14 -date: 08/31/025. ibuprofen and famotidine tablets, 800 mg/26.6 mg, 90 tablets per bottle. Manufactured by: Alkem Laboratories Ltd. Lot #: 23140190, exp.
2024/4/4 -This recall should be conducted to the RETAIL level. PRODUCT NAME: Ibuprofen and Famotidine Tablets, 800/26.6 mg. LOT NUMBER: 23140190. NDC NUMBER: 67877-626 ...
6日前 -Firm Press Release: Exela Pharma Sciences, LLC Issues Voluntary Nationwide Recall of Ibuprofen Lysine Injection, 20 Mg/2 Ml (10 Mg/Ml) Due to Particulate ...
2024/5/4 -Class 1 Recall: Reasonable probability that using the drug will cause ... Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis.
2024/6/4 -Examples of drug mislabeling issues that could prompt a recall include: Missing label. Label placed on wrong drug (such as an ibuprofen bottle labeled as ...
2024/6/12 -There was also a recall of CVS own-brand ibuprofen tablets that same year after investigators found the pills contained more of the painkiller than the label ...
5日前 -Oral ibuprofen, Drugs, Generic Drugs, Higher Concentration of Ibuprofen, Tris Pharma, Inc. Terminated. 528, 03/23/2020, Ranier's RX Laboratory, Compounded drug ...
2024/2/1 -For Class 2 recalls, there is a potential for serious adverse events but a lower chance of the drug causing serious injury or death than in a Class 1 recall.
2024/4/22 -(Par), is expanding its voluntary recall to include seven lots of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product is being recalled ...
2024/6/27 -Exela Pharma Sciences with X-Gen announced a voluntary recall of Ibuprofen Lysine Injection 20mg/2mL (10mg/mL) vials due to the presence of particulate matter.