Recalls Archive

About the Recall: Cardinal Health has notified McKesson Medical-Surgical Inc. (MMS) of an Urgent Product Notice regarding specific lot(s) of their Various Monoject Syringes. This notice has been issued because the Cardinal Health Monoject™ Luer-lock tip syringes (1, 6, 12, 20, 35 and 60 mL) have demonstrated recognition and compatibility…

About the Recall: Smith & Nephew Medical Limited has issued a Medical Device Correction regarding specific lots of their No-Sting SKIN-Prep Wipes and No-Sting SKIN-Prep Swabs due to a manufacturing error resulting in the presence of acetic acid causing a vinegar-like odor and potential minor skin irritation. Products(s) numbers/models that…

About the Recall: Typenex Medical has issued a product notice regarding specific lots of anesthesia and respiratory products distributed by McKesson Medical-Surgical Inc. This issue has been noticed to inform customers of a labeling error with the expiration date format only.  Affected product first shipped on August 1, 2022. Affected…

About the Recall: Voluntary recall of Magic3 Go® Intermittent Silicone Catheters. Our records indicate you may have purchased an affected lot(s) of products between September 22, 2021- March 22, 2023. Products(s) numbers/models that are affected: Identify and check the REF and LOT numbers on your Magic3 Go® product(s) customer box…

About the Recall Medical Device correction, for Trilogy Evo 02, Trilogy Evo Universal, Trilogy EV300, and Trilogy Evo ventilators Affected Products: Model: DS2000X118 Description:Trilogy Evo Universal Ventilator UDI:606959052000 Model:DS2100X11B Description:Trilogy Evo, 02, USA UDI:606959051997 Model:DS2110X11B Description:Trilogy Evo, USA UDI:606959051942 Model:DS2200X11B Description:Trilogy Evo, 02, USA EV300 UDI:606959052017 Model:IN2100X15B Description:Trilogy Evo, 02,…

About the Recall: Medtronic is issuing a voluntary recall for specific production lots of Shiley™ Adult Flexible Tracheostomy Tubes with TaperGuard™ Cuff and Cuffless with Disposable or Reusable Inner Cannulas.  You are receiving this letter because our records indicate you may have purchased items with affected lot numbers. The affected…

About the Recall: Perrigo Company has initiated a voluntary recall regarding specific lots of their Nestle Gerger® Good Start® SoothePro™ Powdered Infant Formula manufactured at the Company’s Gateway manufacturing facility in Eau Claire, Wisconsin, and distributed by McKesson Medical-Surgical. This notice has been issued due to the potential presence of…

About the Recall Medical device correction for the Life2000 ventilation system due to the potential for patient desaturation events that can occur under certain scenarios when connected with an oxygen concentrator. Affected Products: Life2000 ventilation system Manufacturer Notice/Web Site: https://www.hillrom.com/en/products/life2000-system/ Actions to be taken by customer/Patient: Customers who contact AdaptHealth…

About the Recall Voluntary Medical Device Correction to provide information about risks associated with the lithium-ion batteries contained in the FreeStyle Libre, FreeStyle Libre 14 Day and FreeStyle Libre 2 Flash Glucose Monitoring System Readers. Affected Products: FreeStyle Libre, FreeStyle Libre 14 Day and the FreeStyle Libre 2 readers. Manufacturer…

About the Recall: Smiths Medical has issued a voluntary Medical Device Correction for potential issues with CADD Infusion system sets. Smiths Healthcare is implementing this correction due to two issues. Lack of delivery or under-delivery related to tubing occlusion; False “No Disposable Attached (NDA)” alarms The risk for issue 1…