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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

198

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 1321–1340 of 3552 recalls

HAMILTON-H900 Humidifier (Hamilton Medical) - Startup Malfunction (2021)

When starting a humidifier, intended for respiratory gas conditioning during invasive and noninvasive mechanical ventilation, with an empty chamber, and water is not filled into the chamber, the low water level alarm will be delayed and medical staff are unaware that there is no water in the chamber.

FDAJan 5, 2021CA, FL, NV +3 more• Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland

Dole Sesame Asian Chopped Salad Kit – Undeclared Egg (2021)

Undeclared Allergen

Incorrect product master-pack label causing an undeclared allergen; egg.

Class IHigh

FDAJan 5, 2021AK, CA, ID +6 more• Dole Fresh Vegetables Inc

Valanga Gourmet Snickerdoodle Cookie – Undeclared Milk (2020)

The firm declares whey as the margarine's sub-ingredient but does not declare milk.

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Class IIModerate

FDADec 29, 2020IN, OR, WA• Avalanche Distributing, LLC

Auryxia (Akebia Therapeutics) – manufacturing deviation (2020)

CGMP Deviations

Class IIModerate

FDADec 9, 2020Nationwide• Akebia Therapeutics dba Keryx Biopharmaceutials, Inc

Darlington Soft Baked Cookies – Undeclared Milk (2020)

An internal quality review found that an ingredient contained a milk derivative, but milk was not declared on the label.

Class IIILow

FDADec 4, 2020IL, IN, NY• HS Baking Enterprises LLC DBA Darlington Manufacturing

Stryker Medela Aspiration Tubing (Medela) – Expiration Date Error (2020)

Incorrect expiration date of "2023-07-24" on label of sterile tubing. Correct expiration date should be "2021-07-24".

FDADec 2, 2020Nationwide• Medela AG Medical Technology Lattichstrasse 4b Baai Switzerland

Baby Feeding Sets (Herobility) – Choking Hazard (2020)

Choking Hazard

This recall involves Eco Baby Spoons and Forks and Eco Feeding Spoons, as well as the Eco Placemat Feeding sets 4 PCS, because they include the Eco Feeding Spoon. The recalled spoons and forks are made entirely of a plastic compound, and are distinct from the other Herobility spoons and forks sold in the U.S., which consist of plastic handles with steel implements. The Herobility name and, in most instances, the date (month/2019) are located directly on the underside of the recalled products. In addition to products with a date stamp of (month/2019), products with no date stamp are included in the recall.

CPSCNov 25, 2020Nationwide• Herobility AB, of Sweden

Organic Romaine Hearts (Dole) – E. coli contamination (2020)

E. coli

Pathogenic non-O157 E.coli STEC found during routine sampling by Michigan Department of Agriculture and Rural Development.

Class IHigh

FDANov 21, 2020AZ, HI, IL +11 more• Dole Fresh Vegetables Inc

Optilite Freelite Mx Kit (Binding Site) – Quality Control Bias (2020)

Due to customer complaints of positive bias impacting quality control. The high and low level controls are demonstrating a positive bias compared to assigned values.

FDANov 18, 2020CO, FL, IA +7 more• The Binding Site Group, Ltd.

Tempus LS Defibrillator (Remote Diagnostic) – Software Error (2020)

A software error was detected within software version 1.3.4 for the Tempus LS device. When exiting pacer back into manual mode the pacer pulse wave may put the ECG calibration out of calibration. This software error may result in a delay in therapy, as the clinician is not provided an ECG waveform on which a shockable rhythm decision can be made. The device is still able to deliver a manual defibrillation shock.

FDANov 17, 2020Nationwide• Remote Diagnostic Technologies Ltd. PAVILION C2, ASHWOOD PARK ASHWOOD WAY Basingstoke United Kingdom

Coleslaw (Presidents Choice) – processing deviation (2020)

CCP deviation with the wash process

Class IIILow

FDANov 14, 2020IN• Dole Fresh Vegetables Inc

Electric Throw Heated Blankets (InvoSpa) – fire burn hazard (2020)

Fire/Burn Risk

This recall involves InvoSpa electric throw heated blankets. The recalled blankets measure 50 inches by 60 inches. The blankets are made of silky flannel and sherpa shu velveteen and are white and gray. Model number ML-G03 and InvoSpa are printed on a tag on the blanket.

CPSCNov 12, 2020Nationwide• Hebei Yuwang Electrical Appliance Co. Ltd, of China

RayStation Software (RaySearch) – Treatment Report Issue (2020)

Two issues were found with the treatment plan report: 1) There may be incorrect information for the percent of a region of interest with a clinical goal that is outside the dose grid; and 2) For RayStation and RayPlan 9B and 10A, 6D couch angles may be incorrect.

FDANov 11, 2020Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden

K-ACT Clotting Test Tubes (Helena) – Cap Cracking (2020)

Due to complaints received associated with cracked/split test tube caps.

FDANov 9, 2020Nationwide• Helena Laboratories, Corp.

Sentinel Monitor (Spacelabs) – Test Comment Issue (2020)

During system upgrade incorrect comments may be added to existing tests. In such instance: Resting ECG and ABP tests which did not contain comments at the time of the upgrade, may have unrelated comments added. Existing comments will not be overwritten or removed. Rhythm ECG Tests may have comments overwritten with unrelated comments. Any tests created after the upgrade are not affected.

FDANov 6, 2020Nationwide• Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom

MassChrom Amino Acid Control (Chromsystems) – Stability Criteria (2020)

Products do not meet stability criteria and may impact results.

FDANov 2, 2020Nationwide• Chromsystems Instruments & Chemicals GmbH Am Haag 12 Grafelfing Germany

3PLUS1 Multilevel Plasma Calibrator (Chromsystems) – Stability Criteria (2020)

Products do not meet stability criteria and may impact results.

FDANov 2, 2020Nationwide• Chromsystems Instruments & Chemicals GmbH Am Haag 12 Grafelfing Germany

MassChrom Cortisol Control (Chromsystems) – Stability Criteria (2020)

Control lots may not meet stability criteria and could result in increased results of patient samples for cortisone.

FDAOct 29, 2020Nationwide• Chromsystems Instruments & Chemicals GmbH Am Haag 12 Grafelfing Germany

6PLUS1 Saliva Calibrator (Chromsystems) – Stability Criteria (2020)

Calibrator lots may not meet stability criteria and could result in increased results of patient samples for cortisone.

FDAOct 29, 2020Nationwide• Chromsystems Instruments & Chemicals GmbH Am Haag 12 Grafelfing Germany

Surgeloc Surge Devices (Schneider Electric) – Fire Hazard (2020)

Fire/Burn Risk

This recall involves Schneider Electric Surgeloc Surge Protection Devices. The 3-wire and 4-wire devices are primarily installed in commercial/industrial applications and may include some residential applications. They are black rectangular-shaped devices with a green plastic rimmed meter and a white label with "Square D by Schneider Electric," with the date code and the catalog number on the front. The recalled devices were manufactured from January 1, 2013 (date code 13011) through August 24, 2020 (date code 20352). The date codes are in the YYWWD format (example: 20452 = year 2020, week 45, day 2 Monday; the day is optional). The date code is located on the front of the device. Catalog numbers included in the recall include the following: Voltage Surge Current Rating NQ Panelboard Units - Surge Cat No. 120/240 V, 1 Phase, 3-wire + ground 80 kA SSP01BIA08PBQ1 100 kA SSP01BIA10PBQ1 120 kA SSP01BIA12PBQ1 160 kA SSP01BIA16PBQ1 200 kA SSP01BIA20PBQ1 240kA SSP01BIA24PBQ1 208Y/120 V, 3-Phase, 4-wire + ground Wye 80 kA SSP02BIA08PBQ1 100 kA SSP02BIA10PBQ1 120 kA SSP02BIA12PBQ1 160 kA SSP02BIA16PBQ1 200 kA SSP03BIA20PBQ1 240kA SSP03BIA24PBQ1 240Y/120 V, 3-Phase, 4-wire + ground High-leg Delta 80 kA SSP03BIA08PBQ1 100 kA SSP03BIA10PBQ1 120 kA SSP03BIA12PBQ1 160 kA SSP03BIA16PBQ1 200 kA SSP03BIA20PBQ1 240kA SSP03BIA24PBQ1

CPSCOct 28, 2020Nationwide• Schneider Electric Systems USA, Inc., of Foxboro, Mass.