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Kamiya Biomedical Company, LLC

Kamiya Biomedical Company, LLC Recalls

All product recalls associated with Kamiya Biomedical Company, LLC.

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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 4941–4960 of 21320 recalls

K-ASSAY IgA Immunoturbidimetric (Kamiya) – Reagent Cloudiness (2022)

IgA Reagent may start showing cloudiness over time, which can affect assay performance.

Low

FDASep 28, 2022Nationwide• Kamiya Biomedical Company, LLC

biokitHSV-2 Rapid Test (Biokit) – False Positive Risk (2022)

HSV-2 rapid test may report false positive results.

High

FDASep 28, 2022Nationwide• Biokit, S.A. Avinguda De Can Montcau 7 (Barcelona) Llica D'Amunt Spain

Acyclovir Sodium Injection (AuroMedics) – particulate matter (2022)

Presence of Particulate Matter: Customer complaint for a dark red, brown and black particulate floating inside vial.

Class IIModerate

1...246 247248249 250...1066

Page 248 of 1066Next

FDA

Sep 26, 2022

Nationwide

• AuroMedics Pharma LLC

Tranexamic Acid Injection (AuroMedics) – metal contamination (2022)

Presence of Particulate Matter: Piece of metal found in a vial

Class IIILow

FDASep 26, 2022Nationwide• AuroMedics Pharma LLC

Micro Bird G5 School Bus (Micro Bird) – Electrical Cable Problem (2022)

Fire/Burn Risk

Corp. Micro Bird, Inc. (Micro) is recalling certain 2012-2023 G5, 2012-2023 MBII and 2015-2022 T-Series school buses. The power cable that provides electricity to the air conditioning control board may have a loose connection to the power stud on the board.

High

NHTSASep 23, 2022Nationwide• MICRO BIRD

Micro Bird MB II (Micro Bird) – Electrical Cable Problem (2022)

Fire/Burn Risk

Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2013-2022 G5, 2015-2019 T-Series, and 2012-2015 MBII transit buses. The power cable that provides electricity to the air conditioning control board may have a loose connection to the power stud on the board.

High

NHTSASep 23, 2022Nationwide• MICRO BIRD

Hamilton-C6 (Hamilton Medical) – Screen Backlight Problem (2022)

Due to a malfunction related to the backlight on the ventilator screen. The screen goes black for approximately 2-3 seconds, but it brightens up again when the backlight switches on again.

Moderate

FDASep 22, 2022Nationwide• Hamilton Medical AG Parc Industrial Vial 10 Domat/Ems Switzerland

Bunk Bed Ladders (Canyon Furniture) – Entrapment Risk (2022)

This recall involves ladders sold as part of a furniture set, including Cottage Colors and Canyon Lake bunk bed configurations that include desk- or dresser-top hutches. The recalled ladders were sold in various combinations with bunk beds and hutches. The ladders have the following SKU numbers, which are printed on a label on the underside of a ladder step. This recall includes only ladders sold with the Canyon Lake and Cottage Colors bunk bed configurations that include a desk- or dresser-top hutch. Brand Name Color of Ladder SKU Canyon Lake Java ladder 35834008 Ash gray ladder 35834010 Cottage Colors White ladder 36428008 Black ladder 36428010 Gray ladder 36428022

High

CPSCSep 22, 2022Nationwide• Montecitos Manufacturing, of Mexico

WEB Detachment Controller (MicroVention) – Implant Device Risk (2022)

Detachment controller, of an aneurysm embolization system, has an out of specification tunnel opening dimension, which may prevent the implant device pusher from being fully inserted into the controller, which may result in the inability of the controller to properly detach the implant device, which could cause delays and excessive manipulation that may cause the implant to move and damage vessels

High

FDASep 21, 2022Nationwide• MICROVENTION INC.

MiniMed Insulin Pump (Medtronic) – Cybersecurity Vulnerability (2022)

Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series Insulin Pump Systems associated with the communication protocol that could allow unauthorized access to the pump system. This unauthorized access could be used to deliver too much or too little insulin through delivery of an unintended insulin bolus or because insulin delivery is slowed or stopped, which could lead to hypoglycemia or hyperglycemia. The Remote Bolus feature on insulin pumps should be turned off to prevent the unauthorized access.

Very High

FDASep 20, 2022AL, AK, AZ +49 more• Medtronic MiniMed

da Vinci X (Intuitive Surgical) – Inadvertent Energy Delivery (2022)

Inadvertent energy delivery from surgical system instrument if 1) Force bipolar and bipolar instruments installed on system 2) Force bipolar connected to Force Triad generator, bipolar not connected to generator 3) Yellow pedal associated with force bipolar is pressed, released with head in surgeon console 4) Blue pedal associated with bipolar is pressed, resulting in force bipolar energy delivery

High

FDASep 20, 2022AL, AK, AZ +24 more• Intuitive Surgical, Inc.

MiniMed Insulin Pump (Medtronic) – Cybersecurity Vulnerability (2022)

Very High

FDASep 20, 2022AL, AK, AZ +49 more• Medtronic MiniMed

Vortex MP Port (Angiodynamics) – Missing Instructions (2022)

Printed Instructions for Use (IFU) not shipped with device. The Instructions for Use contain the Warnings, Precautions, Contraindications, and Procedures for the Preparation, Implantation, and Post Operative Care of the implantable port, failure to follow the Instructions for Use may result in patient injury.

Moderate

FDASep 20, 2022Nationwide• Angiodynamics, Inc.

ARTIS pheno X-Ray System (Siemens) – Software Issue (2022)

Siemens has become aware of three potential software issues with ARTIS pheno systems with software version VE10B. This may lead to a hazardous situation for patients if treatment cannot be continued on the system and treatment needs to be continued on an alternate system.

Moderate

FDASep 20, 2022Nationwide• Siemens Medical Solutions USA, Inc

STRATAFIX SPIRAL PGA-PCL (Ethicon) – Incorrect Needle Type (2022)

Laceration Risk

Packages may contain a PS-1 cutting edge needle and not the intended SH taper point needle may result in more tissue trauma than is anticipated for taper point needles, which may necessitate repair

Moderate

FDASep 20, 2022Nationwide• Ethicon, Inc. Us

Atellica CH Lithium Test (Siemens) – False Results Risk (2022)

Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930 Analyzer. In the worst case, there is a potential for erroneously elevated lithium patient results, which may lead to inappropriate dosage adjustment, potentially affecting treatment efficacy.

Moderate

FDASep 19, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

Atellica CH Lithium Test (Siemens) – False Results Risk (2022)

Moderate

FDASep 19, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

Clonidine Hydrochloride Tablets (UNICHEM) – Product Mix-up (2022)

Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,

Class IIILow

FDASep 19, 2022Nationwide• UNICHEM PHARMACEUTICALS USA INC

Berkeley VC-10 System (Olympus) – IFU Update (2022)

Update to the Instruction for Use (IFU): Olympus is adding a new warning against the use of accessories which are not listed in the IFU. There have been reported adverse events involving the use of collection canisters which were not designed for use with the VC-10, which can lead to serious injuries as it does not fit properly with the VC-10.

High

FDASep 16, 2022Nationwide• Olympus Corporation of the Americas

Prep-Fill Connector (IMI) – Compromised Sterility (2022)

Blister package had an unsealed edge compromising sterility.

High

FDASep 16, 2022Nationwide• International Medical Industries, Inc.