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Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland

Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland Recalls

All product recalls associated with Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland.

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Recall Summary

Total Recalls

1000

Past Year

206

Class I (Serious)

410

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 561–580 of 3552 recalls

Hamilton-C6 Ventilator (Hamilton Medical) – safety ventilation error (2023)

Software error causes, safety ventilation, in which ventilation continues in the "safety ventilation" mode with audible/visible alarm - patient inputs are not monitored, if the following coincide 1) A mode change to an adaptive mode (ASV, APVcmv, APVsimv, INTELLiVENT-ASV, (S)CMV+, SIMV+), and 2) The controller and/or humidifier is connected to the ventilator and is operational.

FDAMar 14, 2023Nationwide• Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland

Quantum Perfusion Systems (Spectrum Medical) – bobbin lock fault (2023)

The ratchet and pawl had an out of tolerance geometry which exhibited as the left bobbin would not lock.

FDAMar 13, 2023Nationwide• Spectrum Medical Ltd. Harrier 4, Meteor Business Park Cheltenham Road East Gloucester United Kingdom

REX Pressure Therapy System (Compass Health) – User Manual Error (2023)

Error in the Introduction section of the user manual that indicates the device may be used for the prevention of deep vein thrombosis (DVT). Marketed without a 510k for this indication

1...27 282930 31...178

Page 29 of 178Next

FDAMar 7, 2023Nationwide• Compass Health Brands (Corporate Office)

United Imaging PET System (Shanghai United Imaging) – Scatter Correction Failure (2023)

Due to a software issue where the process of patient scanning, the scatter correction may occasionally fail with will potentially cause a failure of the PET image reconstruction and generation of PET images.

FDAMar 1, 2023Nationwide• Shanghai United Imaging Healthcare Co., Ltd. No. 2258 Chengbei Rd, Jiading Ind. Shanghai China

Tempus Pro Patient Monitor (Remote Diagnostic) - Safety Issues (2023)

During internal testing, Regulatory Compliance issues were identified regarding the Monitor and Power Supplies for fluid ingress and basic safety issues.

FDAFeb 23, 2023Nationwide• Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom

2D Perfusion (Philips) - Signal Processing (2023)

There are technical issues related to signal generation and processing, which can lead to inaccurate presentations.

FDAFeb 20, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

SmartPerfusion (Philips) - Signal Processing (2023)

There are technical issues related to signal generation and processing, which can lead to inaccurate presentations.

FDAFeb 20, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Raystation Treatment Planning (RaySearch) - Collimator Angle (2023)

It is possible to set a non-zero collimator angle in the Virtual Simulation module. The angle will be correct in the user interface but if the plan is DICOM exported by using the VSIM Export button, the angle will not be correct in the exported RT plan. In the exported RT plan, the DICOM attribute Beam Limiting Device Angle (300A,0120) is set to zero, regardless of the selected collimator angle.

FDAFeb 17, 2023Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

Electric Bicycles (Linus Bike) – Crash hazard (2023)

This recall involves the Linus Bike Cesta 500 and Ero 500 electric bicycles. The serial number can be found on the underside of the frame near the chain ring. The brand name "Linus" is printed on the frame of the bicycle. The recalled bicycles have one of the following serial numbers. Product Name Serial Number Ero500/Cesta500 LXD20100231-LXD20100420 Ero500/Cesta500 LXD20100686- LXD20100830 Ero500/Cesta500 LXD20100956- LXD20101060

CPSCFeb 16, 2023Nationwide• Shenzhen Xidesheng Bicycle Co Ltd, of China

Sheetz Ham Deli Sandwich – Undeclared sesame (2023)

Undeclared Allergen

Product may contain undeclared sesame

Class IIModerate

FDAFeb 16, 2023IN, MD, NC +4 more• Sheetz Distribution Services, L.L.C.

Sheetz Turkey Deli Sandwich – Undeclared sesame (2023)

Undeclared Allergen

Product may contain undeclared sesame.

Class IIModerate

FDAFeb 16, 2023IN, MD, NC +4 more• Sheetz Distribution Services, L.L.C.

PrimeZEN Black Capsules (Volt Candy) – Undeclared Drug Ingredients (2023)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Class IHigh

FDAFeb 13, 2023Nationwide• Volt Candy Wholesale Club

Bistro To Go Fresh Cut Pineapple Chunks (Fresh Creative Cuisine) – potential contamination (2023)

Listeria

On 02/03/2023, FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine of Baltimore, MD is initiating a recall of various products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated with Listeria monocytogenes .

Class IHigh

FDAFeb 3, 2023CT, DE, MD +8 more• FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine