Shots: Medtronic has recalled its MiniMed 600 Series Insulin Pumps due to missing or broken retainer ring which helps to lock the insulin cartridge leading towards under/ over the delivery […]Read More
Tags : Recalls
Shots: The voluntarily nationwide consumer level recall involves three lots of Nizatidine Capsules (including the 150mg and 300mg strengths) due to trace amounts of NDMA contained in API Nizatidine, USP, […]Read More
Shots: Smith Medical has recalled its Medfusion 4000 syringe pump with firmware version 1.7.0 due to malfunctioning alarms and potential interruption of therapy. The FDA has labeled it as Class […]Read More
Shots: Sandoz recalls all quantities and lots of ranitidine hydrochloride capsules (150/300mg) including 30 count, 60 count and 500 count bottles within expiry to the consumer level due to an […]Read More
Shots: Takeda is issuing a recall for all doses of Natpara for injection (25/50/75/100 mcg) in the US after the discussion with US FDA due to the potential for rubber […]Read More
Shots: Sandoz recalls ~636,000 of Losartan potassium and Ezetimibe prescription drug bottles due to failure to meet child-resistant closure requirements as required by the Poison Prevention Packaging Act, posing a […]Read More
Shots: Allergan voluntarily recalls BIOCELL textured breast implants and tissue expander as a precaution following the US FDA’s notification on global safety of breast implant-associated with anaplastic large cell lymphoma […]Read More
Shots: Fresenius Kabi voluntarily recalls two lots of Fluorouracil Injection with a lot number 6120341 and 6120420 to the consumer level due to the presence of glass particulate, distributed between […]Read More
Shots: Ethicon recalls Endo-Surgery Curved Intraluminal Stapler & Endo-Surgery Endoscopic Curved Intraluminal Stapler with adjustable height staples manufactured from Mar’18 to Mar’19, categorized by FDA under Class I recall causing […]Read More
Shots: Novartis recalls three lots of Promacta oral suspension to the consumer level due to the presence of peanut floor contamination occurred at third-party manufacturing facility and is conducted within […]Read More
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