ig4 System V2, 120V, 60Hz SYS-2000Recalls & reported problems
Veran Medical Technologies Inc. · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00815686020064), received between Dec 3, 2019 and Dec 3, 2019 — classified as 1 injury.
1 FDA recall record name this device's identifier, 1 still open.
12 other recalls cover devices cleared under the same FDA submission (K122106); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Aug 10, 2023Open, Classified
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
Z-2659-2023 · Root cause: Under Investigation by firm · FDA record ↗
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Pneumothorax1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 3, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
SYSTEM PERFORMED AS INTENDED; NO MALFUNCTION. THREE HOURS AFTER THE CASE WAS FINISHED, WE WERE TOLD THE PATIENT SUFFERED A PNEUMOTHORAX WHILE STILL AT THE HOSPITAL. A CHEST TUBE WAS PLACED, AND THE PATIENT IS IN STABLE CONDITION. DOCTOR EXPECTED THE LEARNING CURVE TO POSSIBLY INCLUDE A PNEUMOTHORAX BUT WAS NOT CONCERNED WITH IT.
Patient problems: Pneumothorax
MAUDE report 9401564 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K122106. One submission often covers many models, so check the product and lot details in each record.
- Z-2663-2023 · Aug 10, 2023 · Open, ClassifiedVeran : Percutaneous Always on Track Models: INS-5040 Always-On vTrack Universal Tracker, LG 7-12ga INS-5039 Always-On vTrack Universal Tracker, SM/CL, 12-18ga INS-5036 "
- Z-2662-2023 · Aug 10, 2023 · Open, ClassifiedVeran : Endobronchial Models: INS-5500 View Optical Probe INS-5450 SPiN Xtend 21ga, 1.8 OD, 5/Bx INS-5440 View Peripheral Catheter, 3.8mm OD, 2.5mm WC INS-5411 0.016
- Z-2661-2023 · Aug 10, 2023 · Open, ClassifiedVeran : Percutaneous Models: INS-5620 SPiN Perc Biopsy Needle Guide Kit - 20cm, 5/Bx (includes INS-5028)" INS-5611 SPiN Perc Localization Needle - 2cm, 5/Bx INS-5610 SPiN
- Z-2664-2023 · Aug 10, 2023 · Open, ClassifiedVeran : 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 For
- Z-2266-2023 · May 15, 2023 · Open, ClassifiedAlways-On Tip Tracked Instruments (SPiN Drive instruments) 21ga ANSO Cytology Needle, 12mm L, 1.8mm OD-Intended for use in clinical interventions and for anatomical structures wher
- Z-2264-2023 · May 15, 2023 · Open, ClassifiedAlways-On Tip Tracked Instruments (SPiN Drive instruments) Forceps, 1.8mm OD, Serrated Cup-Intended for use in clinical interventions and for anatomical structures where computed t
- Z-2267-2023 · May 15, 2023 · Open, ClassifiedAlways-On Tip Tracked Instruments (SPiN Drive instruments) Triple Needle Brush, 12mm L, 1.8mm OD-Intended for use in clinical interventions and for anatomical structures where comp
- Z-2262-2023 · May 15, 2023 · Open, ClassifiedAlways-On Tip Tracked Instruments (SPiN Drive instruments) Brush, 15mm L, 1.8mm OD Intended for use in clinical interventions and for anatomical structures where computed tomograph
- Z-2265-2023 · May 15, 2023 · Open, ClassifiedAlways-On Tip Tracked Instruments (SPiN Drive instruments) 19ga ANSO Histology Needle, 12mm L, 1.8mm OD-Intended for use in clinical interventions and for anatomical structures whe
- Z-2269-2023 · May 15, 2023 · Open, ClassifiedAlways-On Tip Tracked Instruments (SPiN Drive instruments) SPiN Xtend 2.0mm OD, 21ga Intended for use in clinical interventions and for anatomical structures where computed tomogr
- Z-2263-2023 · May 15, 2023 · Open, ClassifiedAlways-On Tip Tracked Instruments (SPiN Drive instruments) Forceps, 1.8 mm OD, Oval Cup-Intended for use in clinical interventions and for anatomical structures where computed tomo
- Z-2268-2023 · May 15, 2023 · Open, ClassifiedAlways-On Tip Tracked Instruments (SPiN Drive instruments) 22ga SPiN Flex Needle, 12mm L, 1.8mm OD-Intended for use in clinical interventions and for anatomical structures where co
Other System, X-Ray, Tomography, Computed devices
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- ARTIS icono floor 11327700Siemens Healthcare GmbH · System, x-ray, tomography, computed15 recalls24 reports
- Incisive CTPhilips Healthcare (Suzhou) Co., Ltd. · System, x-ray, tomography, computed13 recalls5 reports
- Spectral CTPhilips Medical Systems Nederland B.V. · System, x-ray, tomography, computed11 recalls3 reports
- Incisive CTPhilips Healthcare (Suzhou) Co., Ltd. · System, X-Ray, Tomography, Computed9 recalls20 reports
- Brilliance iCTPhilips Medical Systems Nederland B.V. · System, x-ray, tomography, computed8 recalls6 reports
- Revolution Apex EliteGE Medical Systems, L.L.C. · System, x-ray, tomography, computed8 recalls0 reports
- Brilliance CT Big BorePhilips Medical Systems Nederland B.V. · System, x-ray, tomography, computed7 recalls1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.