medical Class II Updated 2023-10-11

Olympus Corporation of the Americas recalls Veran : Endobronchial Always on Track Models: INS-0392 AOT

Recalled Product

Veran : Endobronchial Always on Track Models: INS-0392 AOTT 21ga Needle, 12mm L, 1.8mm OD, 5/BX INS-0382 AOTT 19ga Needle, 12mm L, 1.8 OD, 5/Bx INS-0372 AOTT Serrated Forceps, 1.8mm OD, 5/Bx INS-0362 AOTT Oval Cup Forceps, 1.8mm OD, 5/Bx INS-0352 "Always-On Tip Tracked (AOTT) Brush, 15mm L, 1.8mm OD, 5/Bx" INS-0322 View Peripheral Catheter, 3.2mm OD, 2.0mm WC INS-0305 Always-On Tip Tracked Guidewire, 1.0mm, 950mm INS-0304 Always-On Tip Tracked Guidewire, 1.0mm, 735mm INS-0050 vPad Patient Tracker, 5/Bx INS-0048 vPad Connector Cable

Hazard / Issue

Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic Navigation System, SPiN Planning Laptop Workstation, and all associated navigation instruments) manufacturing to design requirements and insufficient evidence to demonstrate adequate electromagnetic compatibility (EMC). EMC is the ability of electrical equipment and systems to function acceptably without interference and to not interfere with other devices within its operating environment

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: INS-0392 AOTT 21ga Needle, 12mm L, 1.8mm OD, 5/BX 00815686020613; INS-0382 AOTT 19ga Needle, 12mm L, 1.8 OD, 5/Bx 00815686020590; INS-0372 AOTT Serrated Forceps, 1.8mm OD, 5/Bx 00815686020576; INS-0362 AOTT Oval Cup Forceps, 1.8mm OD, 5/Bx 00815686020538; INS-0352 "Always-On Tip Tracked (AOTT) Brush, 15mm L, 1.8mm OD, 5/Bx" 00815686020538; INS-0322 View Peripheral Catheter, 3.2mm OD, 2.0mm WC 00815686020477; INS-0305 Always-On Tip Tracked Guidewire, 1.0mm, 950mm 00815686020446; INS-0304 Always-On Tip Tracked Guidewire, 1.0mm, 735mm 00815686020439; INS-0050 vPad Patient Tracker, 5/Bx 00815686020408; INS-0048 vPad Connector Cable 00815686020392; All serial numbers and all lot numbers
View official government recall

Looking for safe alternatives?

Browse certified-safe products in this category on Amazon →

Related medical Recalls

Boston Scientific Corporation recalls Boston Scientific Guider Softip XF, 40 XF, 8F, Guide Cathete

2022-08-31 · The impacted products were distributed with an MPXF tip curve shape instead of the 40XF tip curve shape for the Guider/40XF/8FR/90CM guide catheter.

Mckesson Medical-Surgical Inc. Corporate Office recalls MEDLINE INDUSTRIES Medline Plug, Catheter Medline Plastic, w

2022-08-31 · Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

GE Healthcare, LLC recalls (1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (

2022-08-31 · Inaccurate Distance and Area measurements with use of Global Stack viewport.

Mckesson Medical-Surgical Inc. Corporate Office recalls B. BRAUN MEDICAL INC. Anesthesia Support Tray SUPPORT TRAY,

2022-08-31 · Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.