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 of insulin resulting in hypoglycemic/ hyperglycemic events. The FDA has labeled it as Class I recall The recall involves 322,005 pumps, Model 630G (MMT-1715) & […]Read More
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, manufactured by Mylan Pharmaceuticals Inc The recall is for the lots distributed between Jun, 2017 to Aug, 2018. Additionally, the recall is being conducted under […]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 I recall The 627 devices have recalled having model numbers are 4000-0107-01 and 4000-0106-01, manufactured on Jun 25, 2019, and distributed b/w Sept 27, 2019, […]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 elevated amount of impurity of NDMA which is classified as a carcinogen in the US. The recall is being conducted with the knowledge of the […]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 particulate instigating from the rubber septum of the NATPARA cartridge Takeda is advising patients to consult with their healthcare providers about the discontinuation of Natpara […]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 poisoning risk if swallowed by children The products affected by the recall has distributed by Sandoz in the US includes Ezetimibe in 10mg tablets in […]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 (BIA-ALCL) The global recall of BIOCELL has no effect on Allergan’s NATRELLE smooth or MICROCELL breast implants and tissue. The US FDA has not recommended […]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 Dec 06, 2018 & Feb 20, 2019 Fresenius Kabi notifies its distributors and customers via letter to immediately check their stock and discontinue the utilization […]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 serious injuries or death The recall is due to defect in the washers of staplers resulting in insufficient firing and failure in complete 360-degree staple […]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 the knowledge of the US FDA The voluntary recall is done for the lot numbers 8H57901589, 9H57900189 & 9H57900289 with no reported adverse event till […]Read More
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