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Hamilton Medical, Inc.

Hamilton Medical, Inc. Recalls

All product recalls associated with Hamilton Medical, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 3821–3840 of 25002 recalls

Hamilton-MR1 Ventilator (Hamilton) – control board leak (2023)

Degrading capacitors on the control board of ventilators and spare parts may leak electrolyte onto the control board causing a short circuit on the board and/or the capacitor to lose function and lead to interruption of ventilation.

Moderate

FDAJul 26, 2023Nationwide• Hamilton Medical, Inc.

Instacure #1 (The Sausage Maker) – metal contamination (2023)

Contains Sodium Nitrite recalled for potential metal contamination

Class IIILow

FDAJul 25, 2023Nationwide• The Sausage Maker, Inc.

Allison Transmission 6th Gen TCM (Allison) – Control Module Issue (2023)

Allison Transmission, Inc. (ATI) is recalling certain Emergency Vehicle Series 6th Generation Transmission Control Modules (TCM). The transmission control module (TCM) may fail to achieve the 4th gear transmission lockup needed to initiate the water pump.

1...190 191192193 194...1251

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Moderate

NHTSAJul 24, 2023Nationwide• ALLISON TRANSMISSION

Ambu aView 2 Monitor (Ambu) – Circuit Short Risk (2023)

Multiple impacts, for example from being dropped, can cause to the Ambu aView 2 Advance to short-circuit and under special circumstances make the lithium-ion battery in the device combust leading to smoke and flames

Moderate

FDAJul 21, 2023Nationwide• Ambu Inc.

Rufinamide Tablets 400mg (Aurobindo) – Premature Batch Release (2023)

cGMP deviations: Batch was released prior to approval.

Class IIModerate

FDAJul 21, 2023Nationwide• Aurobindo Pharma USA Inc.

Rufinamide Tablets 200mg (Aurobindo) – Premature Batch Release (2023)

cGMP deviations: Batch was released prior to approval.

Class IIModerate

FDAJul 21, 2023Nationwide• Aurobindo Pharma USA Inc.

Neurosurgical Trocar (Aesculap) – Manufacturing Length Issue (2023)

Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30 neuroendoscope, a portion of the visual field is obscured.

Moderate

FDAJul 20, 2023Nationwide• Aesculap Implant Systems LLC

Visera Hysterovideoscope (Olympus) – Labeling Update (2023)

IFU labeling is being updated to revise EtO gas mixture and elimination of reusable cleaning brushes.

Low

FDAJul 20, 2023Nationwide• Olympus Corporation of the Americas

Fentanyl-Bupivacaine Solution (SCA Pharma) – Rejected Units Shipped (2023)

cGMP deviations: due to shipment of rejected units.

Class IIModerate

FDAJul 20, 2023KY, NJ• SCA Pharmaceuticals

Zenition 70 (Philips) – Radiation Exposure Risk (2023)

Philips has become aware of the potential for unintended radiation exposure with Zenition 70 systems with Vascular Extension option and a Wireless Foot Switch.

Moderate

FDAJul 20, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Azurion (Philips) – Unintended Radiation Emission (2023)

A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation

Moderate

FDAJul 19, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Allura Xper Series (Philips) – Unintended Radiation Emission (2023)

A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation

Moderate

FDAJul 19, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

MultiDiagnost-Eleva (Philips) – Unintended Radiation Emission (2023)

A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation

Moderate

FDAJul 19, 2023Nationwide• Philips Medical Systems Nederland B.V. High Tech Campus 36 Eindhoven Netherlands

Randox Liquid Protein Calibrator (Randox) – Ferritin Restandardization (2023)

As part of the firm's ongoing quality monitoring (see internal complaint # OCC72574), Randox Laboratories have restandardized Ferritin in Liquid Protein Calibrators, IT2691, to reference material NISBC 19/118. The calibrators lots 2112IT-2116IT, packed into batches 627222, 627224, 634886 and 634887 have been reassigned as part of the restandardization. Following this restandardization, Ferritin results for Quality Control material and patient samples recovered erroneously higher than the targeted calibrator values by approximately +10% across the assay range following.

Moderate

FDAJul 19, 2023CA, FL, IL +6 more• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland