Search U.S. Product Recalls Database

Showing 6761–6780 of 8393 results

Sort:

NIM EMG Endotracheal Tube (Medtronic) – airway obstruction (2022)

The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.

FDAApr 29, 2022Nationwide• Medtronic Xomed, Inc.

Adult Cap-ONE Biteblock (Nihon Kohden) – expiration problem (2022)

Due to products being shipped/distributed to customers after the products expiration date had past.

FDAApr 29, 2022Nationwide• Nihon Kohden America Inc

Stay Informed

Search Product Recalls

NIM EMG Endotracheal Tube (Medtronic) – airway obstruction (2022)

Adult Cap-ONE Biteblock (Nihon Kohden) – expiration problem (2022)

Centricity Cardiology CA1000 (GE Healthcare) – measurement inaccuracy (2022)

Centricity Enterprise Web (GE Healthcare) – measurement inaccuracy (2022)

Centricity Radiology RA600 (GE Healthcare) – measurement inaccuracy (2022)

Sodium Bicarbonate System (Isopure) – electrical short risk (2022)

Centricity Universal Viewer (GE Healthcare) – measurement inaccuracy (2022)

Centricity PACS RA1000 (GE Healthcare) – measurement inaccuracy (2022)

X80 RADiant Therapy System (Xstrahl) – compatibility issue (2022)

Axium Detachable Coil System (Micro Therapeutics) – labeling error (2022)

4 Series CX Phototherapy (Daavlin) – calibration software issue (2022)

1 Series CX Phototherapy (Daavlin) – calibration software issue (2022)

BVI Wet-Field Eraser (Beaver Visitec) – incorrect product (2022)

Avance CS2 Backup Batteries (GE Healthcare) – early failure (2022)

GE Healthcare Backup Batteries (GE Healthcare) – early failure (2022)

Surgical Suture Kit (Stradis) – sterile barrier uncertainty (2022)

Ivenix Infusion System (Fresenius) – pump start-up time (2022)

SUR-FIT Natura Wafer (ConvaTec) – skin barrier issue (2022)

INTERTAN Nail (Smith & Nephew) – left-right labeling error (2022)

EVIS EXERA II Videoscope (Olympus) – part replacement error (2022)