Recalls Archive

About the recall:     Specific products(s) numbers/models that are affected: Astral 100 and 150 Actions to be taken by customer/Patient: Contact your DME provider.

About the Recall: Clear overview of recall and products affected Voluntarily “Urgent Medical Device Correction” for the M5071A Adult and M5072A Infant/Child Pads Cartridge for use with HS1/Onsite/Home AEDs. Specific products(s) numbers/models that are affected: M5071A Adult and M5072A Infant/Child Pads Cartridge for use with HS1/Onsite/Home AEDs. Manufacturer Notice/Web Site:…

About the Recall: The Membrane Changers (REF: MC, MC-R and MC-I) are used to change the membranes on your V-Sign™ 2 or OxiVenT™ sensors. This is part of routine maintenance as outlined in the Instruction Manuals (HB-005771-r, HB-011077-_, HB-005147-m, HB-006417-d). What is the defect? During the manufacturing process there were…

About the Recall: Company has notified McKesson Medical-Surgical Inc. (MMS) of an Urgent Drug/Product/Medical Device Information/Safety Notification regarding one/specific lot(s) of their Product Name. This notification has been issued because/due to reason for the notification here. Affected product first shipped June 29, 2013. Specific products(s) numbers/models that are affected: Manufacturer…

About the Recall: Smiths Medical has notified McKesson Medical-Surgical Inc. (MMS) of an Urgent Medical Device Correction regarding specific lots of their CADD™ Infusion System Infusion Sets for use with CADD pumps. This is an update to the notice from 09 December 2022. Smiths Medical has identified additional lots of…

About the Recall: Ascensia Diabetes Care (ADC) has notified McKesson Medical-Surgical Inc. (MMS) of an Urgent Medical Device Recall regarding one lot of their CONTOUR® NEXT Gen Blood Glucose Meters. This notice has been issued because ADC has determined through customer complaints (22 complaints till 15-Jun-2023) that 579 meters distributed…

About the Recall: Teleflex LLC has notified McKesson Medical-Surgical Inc. (MMS) of an Urgent Medical Device Recall regarding specific lots of their Endotracheal Tubes (ET tube). This notice has been issued due to reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.…

About the Notice: ResMed is updating its existing contraindications and warnings to further inform patients and healthcare professionals on the safe use of ResMed masks with magnets. This is in response to new information obtained through post-market surveillance and industry practices related to possible magnetic interference when in close proximity…

Family Medical Supply, LLC is voluntarily recalling medical grade oxygen cylinders that were delivered between May 18, 2023, and October 31, 2023.

About the Recall: Smiths Medical has notified McKesson Medical-Surgical Inc. (MMS) of an Urgent Medical Device Correction regarding one lot of their Bivona Pediatric Tracheostomy Tube. This notice has been issued because Smiths Medical has identified that the manufacturing date was incorrectly included as the expiration date on the unit…