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Inari Medical Oak Canyon

Inari Medical Oak Canyon Recalls

All product recalls associated with Inari Medical Oak Canyon.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 961–980 of 21319 recalls

Artix MT Thrombectomy Device (Inari) – Vessel Range (2025)

Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the radial force on the artery, which has the potential of vascular complications.

Low

FDAApr 8, 2025Nationwide• Inari Medical Oak Canyon

Micro Bird G5 Transit Bus (Micro Bird) – Suspension Bolt (2025)

Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2023 G5 transit buses. The u-bolts securing the suspension blades may break.

High

NHTSAApr 8, 2025Nationwide• MICRO BIRD

Micro Bird G5 School Bus (Micro Bird) – Suspension Bolt (2025)

Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2023 G5 school buses. The u-bolts securing the suspension blades may break.

High

NHTSA

1...47 484950 51...1066

Page 49 of 1066Next

Apr 8, 2025

Nationwide

• MICRO BIRD

Microstream Advance CO2 Filter (Philips) – Adapter Disconnection Risk (2025)

Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.

Moderate

FDAApr 7, 2025Nationwide• Philips North America Llc

WCM Series Molding Equipment (Apic Yamada) – FDA Compliance Issue (2025)

Apic Yamada has recently discovered that certain products may be out of compliance with FDA electronic product regulations in that they did not bear a required label.

Low

FDAApr 7, 2025Nationwide• Apic Yamada America

Rover Mobile X-Ray System (Micro-X) – Generator Mechanism Failure (2025)

Potential for internal fastening mechanism within generator of mobile x-Ray to fail.

Moderate

FDAApr 4, 2025NJ, WA, PR• Micro-X Ltd. Unit 14 6 Mab Eastern Promenade Tonsley Australia

KliniTray Tissue Margin Board (Klinika Medical) – Microbial Contamination (2025)

Potential for microbial contamination.

Moderate

FDAApr 4, 2025Nationwide• Klinika Mdical Gmb Achtzehnmorgenweg 6 Usingen Germany

KliniTray Faxitron Plate (Klinika Medical) – Microbial Contamination (2025)

Potential for microbial contamination.

Low

FDAApr 4, 2025Nationwide• Klinika Mdical Gmb Achtzehnmorgenweg 6 Usingen Germany

SOLTIVE Pro SuperPul Laser Instrument (Olympus) – Treatment Parameter Deviation (2025)

Preset treatment parameters are not consistently being used in accordance with the IFU.

Moderate

FDAApr 4, 2025Nationwide• Olympus Corporation of the Americas

Texas Olive Pepperoncini (All American Trading) – contamination risk (2025)

The recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed.

Class IIModerate

FDAApr 4, 2025MS, TX• All American Trading Of Houston, Inc.

Texas Olive Capers (All American Trading) – contamination risk (2025)

The recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed.

Class IIModerate

FDAApr 4, 2025MS, TX• All American Trading Of Houston, Inc.

Texas Olive Giardiniera (All American Trading) – contamination risk (2025)

The recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed.

Class IIModerate

FDAApr 4, 2025MS, TX• All American Trading Of Houston, Inc.

Enhanced Verify Handset (Medtronic) – Communication Malfunction (2025)

Evaluation handsets may not be able to communicate with the neurostimulator due to handsets having a faster processing speed than prior handsets. An inability to connect may cause the therapy to stop being delivered and a system error will be displayed. Patient may experience return of underlying disease symptoms (e.g. overactive bladder, urinary retention, or fecal incontinence) based on their response to stimulation during the evaluation period.

Moderate

FDAApr 3, 2025Nationwide• Medtronic Neuromodulation

MAGEC 2 Rod (Globus Medical) – Incorrect Rod Diameter (2025)

Devices for the affected lot were not assembled according to product specifications. The distraction rod outer diameter was assembled with a 5.5mm rod versus the required 5.0mm.

Low

FDAApr 3, 2025Nationwide• Globus Medical, Inc.

ChlorproMAZINE Tablets (Zydus) – Impurity Above Limit (2025)

CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit

Class IIModerate

FDAApr 3, 2025Nationwide• Zydus Pharmaceuticals (USA) Inc

HistoCore PELORIS 3 (Leica Biosystems) – Tubing Leakage Issue (2025)

There is a leakage issue associated with the tubing in the manifold of the instrument.

Low

FDAApr 2, 2025AZ, CA, FL +11 more• Leica Biosystems Melbourne Pty Ltd

Haloperidol Decanoate Injection (Amerisource) – Sterility Risk (2025)

Lack of assurance of sterility. Bacterial contamination detected in some media fill units

Class IIModerate

FDAApr 2, 2025Nationwide• Amerisource Health Services LLC

Haloperidol Decanoate Injection (Amerisource) – Sterility Risk (2025)

Lack of assurance of sterility. Bacterial contamination detected in some media fill units

Class IIModerate

FDAApr 2, 2025Nationwide• Amerisource Health Services LLC

Haloperidol Decanoate Injection (Amerisource) – Sterility Risk (2025)

Lack of assurance of sterility. Bacterial contamination detected in some media fill units

Class IIModerate

FDAApr 2, 2025Nationwide• Amerisource Health Services LLC

Brilliance CT Big Bore (Philips) – Gantry Motion Risk (2025)

Unintended motion issues related to Interventional Control that may lead to collision of the Gantry/table with the operator or patient.

High

FDAApr 1, 2025Nationwide• Philips North America Llc