Tags : Recalls

Medtronic Recalls its MiniMed 600 Series Insulin Pumps Due to

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

Smith Medical Recalls Medfusion 4000 Syringe Pump Due to its

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

Allergan Voluntary Recalls Worldwide BIOCELL Textured Breast Implants and Tissue

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

Fresenius Kabi Voluntary Recalls Two Lots of Fluorouracil Injection Due

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

Ethicon (J&J) Recalls Endo-Surgery Intraluminal Staplers Due to Complete Staple

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