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Civco Medical Instruments Recalls
45 recalls on record · July 18, 2012 to April 8, 2026 · Medical Devices
Recalls by year
12
14
15
18
21
25
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 16G(for Aurora Trackers), Part Number 667-151
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 14G (for Aurora Trackers), Part Number 667-150
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
June 11, 2025Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or catheter) procedures with the use of diagno
Hazard: During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cover when latching the guide in place.
December 29, 2021Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls VirtuTRAX Instrument Navigator, 10 17 GA VirtuTRAX
Hazard: There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
December 29, 2021Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls VirtuTRAX Instrument Navigator, Sensor with 10 17 GA VirtutTRAX
Hazard: There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
December 29, 2021Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls VirtuTRAX Instrument Navigator, 14 Ga VirtuTRAX
Hazard: There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
December 29, 2021Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls VirtuTRAX Instrument Navigator, Sensor with 14 Ga VirtutTRAX
Hazard: There is potential that the VirtuTRAX device will not tighten onto the instrument to be used.
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Sales Demo Kit, REF DEMOGPGUIDE, for use by CIVCO and customer sales representatives.
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Needle Guide Bracket, REF 674-057-10, Reusable non-sterile bracket for use with FUJIFILM SonoSite, Inc. L25 series
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Needle Guide Bracket, REF 674-057, Reusable non-sterile bracket for use with SonoSite L25 series tranducers, Rx.
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Needle Guide Starter Kit, REF 674-039, Reusable non-sterile bracket with sterile needle guides (1cm, 1.5cm, 2cm de
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Needle Guide Starter Kit, REF 674-038, Reusable non-sterile bracket with sterile needle guide (1cm, 1.5cm, 2cm dep
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Needle Guide Starter Kit, REF 674-037, Reusable non-sterile bracket with sterile needle guides (1.5cm, 2.5cm, 3.5c
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Needle Guide Starter Kit, REF numbers P12924-01 and P12924-02, Reusable non-sterile bracket with sterile (1cm, 1.5
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Needle Guide Starter Kit, REF numbers P12922-01 and P12922-02, Reusable non-sterile bracket with sterile (1cm, 1.5
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Needle Guide Starter Kit, REF numbers P12920-01 and P12920-02, Reusable non-sterile bracket with sterile (1.5cm,
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls SonoSite FUJIFILM Needle Guide Bracket, REF number P06013-08, Reusable non-sterile bracket for use with SonoSite L25 ser
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls SonoSite Needle Guide Bracket, REF numbers P06013-06 and P06013-07, Reusable non-sterile bracket for use with SonoSite L
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Biopsy Bracket, REF P03122-07, Reusable non-sterile single-angle bracket for use with SonoSite L25 series transduc
Hazard: FDA Class II
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Needle Guide Bracket, REF P03122-06, Reusable non-sterile bracket for use with SonoSite L25/L25e transducers, Mfg
Hazard: The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly.
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls SonoSite L25 Bracket Kit containing 1 Reusable non-sterile bracket, REF numbers P03122-01, P03122-02, P03122-03, P03122
Hazard: The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly.
December 19, 2018Medical DevicesFDA
CIVCO Medical Instruments Co., Inc. recalls CIVCO Needle Guide Bracket, REF numbers M001457100, P06013-10, and P03122-08, reusable non-sterile single-angle bracket
Hazard: The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly.
September 5, 2018Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls CIVCO Needle Guide, REF 676-150, QTY 24, STERILE EO
Hazard: The assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide.
September 5, 2018Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls CIVCO Needle Guide, REF 676-144, QTY 24, STERILE EO
Hazard: The assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide.