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Leica Microsystems, Inc.

Leica Microsystems, Inc. Recalls

All product recalls associated with Leica Microsystems, Inc..

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Recall Summary

Total Recalls

1000

Past Year

579

Class I (Serious)

Most Recent

Dec 2025

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 4761–4780 of 10937 recalls

Cryostats (Leica) – Flammable Spray Warning (2019)

The current labelling does not include any specific warning about usage of flammable freezing sprays. Such flammable freezing sprays can potentially ignite and can cause serious injuries.

High

FDAMay 3, 2019AL, AK, AZ +48 more• Leica Microsystems, Inc.

MaxPlus Connector (Becton Dickinson) – Valve Closure Failure (2019)

After disconnection of a luer, the valve of the connector remains recessed; not fully closing, either temporarily or permanently. The risks of blood loss and air embolism exist if the valve remains permanently open and goes undetected, especially in the neonate population.

High

FDAMay 2, 2019Nationwide• Becton Dickinson & Company

Maine Wild Blueberries (Maine Wild Blueberry) – Listeria Risk (2019)

Listeria

Customer found Listeria Monocytogenes in Blueberries after internal sampling. Product was never distributed to consumers.

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Class IHigh

FDAMay 1, 2019IN, MI• Maine Wild Blueberry Company

First Street Dark Chocolate Nonpareils (Heritage Candy) – Almond Mix-up (2019)

Customer discovered that some bags of dark chocolate non pareils contain dark chocolate almonds.

Class IIModerate

FDAMay 1, 2019AZ, CA, NV• Heritage Candy Company

Aquarius D13S319 Probe (Cytocell) – Chromomap Error (2019)

There is an error in the chromomap on the package insert.

Low

FDAApr 26, 2019Nationwide• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

Vitodens Boilers (Viessmann) – carbon monoxide hazard (2019)

This recall involves the Vitodens 200-W and Vitodens 222-F series boilers used for space or domestic water heating. There are five affected models in a specific serial number range. The Vitodens 200-W is a wall hung unit, housed in a white metal box about 38 inches high and 18 inches wide. The Vitodens 222-F is a floor mounted unit, housed in a white metal box about 68 inches tall and 24 inches wide. The name "Vitodens" is printed on the label on the outside of the boiler box. The product name and model number can be found on the left side of the boiler cover. The serial number can be found on the underside of the wall mounted boiler and on the center section on the floor mount model. Product Model Part Number Serial Number Range Vitodens 200-W B2HB 19 7538092 7538092401003107 to 7538092701038106 B2HB 26 7538093 7538093401002107 to 7538093701177109 B2HB 35 7538094 7538094401003101 to 7538094701446103 Vitodens 222-F B2TB 19 7542250 7542250401001100 to 7542250401210106 B2TB 35 7542251 7542251401001107 to 7542251701257105

Very High

CPSCApr 25, 2019Nationwide• Viessmann Werke GmbH & Co KG, of Germany

Linear 3-4 70cm 8 Contact Lead Kit (Boston Scientific) – Voluntary Removal (2019)

The firm is initiating a voluntary removal of certain spinal cord stimulation leads, lead extensions, adapters, and deep brain stimulation lead extensions due to the "use by date" displayed on the label which is later than the correct "use by date". No adverse health consequence is expected to occur from this issue.

Low

FDAApr 24, 2019Nationwide• Boston Scientific Neuromodulation Corporation

Artisan 70cm 2x8 Surgical Lead Kit (Boston Scientific) – Voluntary Removal (2019)

Low

FDAApr 24, 2019Nationwide• Boston Scientific Neuromodulation Corporation

35cm 8 Contact Extension Kit (Boston Scientific) – Voluntary Removal (2019)

Low

FDAApr 24, 2019Nationwide• Boston Scientific Neuromodulation Corporation

55cm 8 Contact Extension Kit (Boston Scientific) – Voluntary Removal (2019)

Low

FDAApr 24, 2019Nationwide• Boston Scientific Neuromodulation Corporation

Linear 3-4 50cm 8 Contact Lead Kit (Boston Scientific) – Voluntary Removal (2019)

Low

FDAApr 24, 2019Nationwide• Boston Scientific Neuromodulation Corporation

Precision M8 Adapter 15cm (Boston Scientific) – Voluntary Removal (2019)

The firm is initiating a voluntary removal of certain spinal cord stimulation leads, lead extensions, adapters, and deep brain stimulation lead extensions due to "use by date" displayed on the label which is later than the correct "use by date". No adverse health consequence is expected to occur from this issue.

Low

FDAApr 24, 2019Nationwide• Boston Scientific Neuromodulation Corporation

IntelliSpace PACS 4.4 (Philips Healthcare) – Image Corruption (2019)

Images may potentially become corrupt while using the system.

Moderate

FDAApr 19, 2019Nationwide• Philips Healthcare Informatics, Inc.

Bevacizumab Injection (Pacifico National) – Delivery System Issue (2019)

Defective Delivery System: difficult to express

Class IIModerate

FDAApr 19, 2019Nationwide• Pacifico National, Inc. dba AmEx Pharmacy

Snowmobiles (Arctic Cat) – fire hazard (2019)

Fire/Burn Risk

This recall involves all Model Year 2018 and 2019 Arctic Cat snowmobile models M8000, XF8000, ZR8000, and Norseman X8000. The vehicles were produced in a variety of color combinations and track lengths. The vehicles all have 8000 on each side of the front hood/side panel area and ARCTIC CAT on the rear snow-flap. The vehicle identification number (VIN) is stamped on the right side of the snowmobile tunnel near the right foot rest.

High

CPSCApr 18, 2019Nationwide• Arctic Cat Inc., of Thief River Falls, Minn.