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Chromsystems Instruments & Chemicals GmbH Am Haag 12 Grafelfing Germany

Chromsystems Instruments & Chemicals GmbH Am Haag 12 Grafelfing Germany Recalls

All product recalls associated with Chromsystems Instruments & Chemicals GmbH Am Haag 12 Grafelfing Germany.

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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 3601–3620 of 10937 recalls

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

Products do not meet stability criteria and may impact results.

Moderate

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.

Moderate

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.

Moderate

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FDA

Oct 29, 2020

Nationwide

• Chromsystems Instruments & Chemicals GmbH Am Haag 12 Grafelfing Germany

Ron Jon Sippy Cup – Lead Content Violation (2020)

This recall involves 13.5-ounce Ron Jon Surf Sippy Cups. The main body of the cup is either orange, blue, pink, or green. There is a rubber-like grip material around the cup. The rubber-like material has images of turtle, crab, fish, boat, and sea grass and the RON JON SURF SHOP design. The product has UPC number 1082-0405 printed on the bottom of the product.

Moderate

CPSCOct 28, 2020Nationwide• Yitak Industry Company Limited, of China

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

High

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

MANI Trocar Kit (Mani) – Luer Connector Failure (2020)

Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use

Moderate

FDAOct 27, 2020Nationwide• Mani, Inc. Kiyohara Facility Park 8-3 Kiyoharakogyodanchi; Kiyoharakogyodanchi; Kiyoharakogyodanchi Utsunomiya Japan

MANI Infusion Cannula (Mani) – Luer Connector Failure (2020)

Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use

Moderate

FDAOct 27, 2020Nationwide• Mani, Inc. Kiyohara Facility Park 8-3 Kiyoharakogyodanchi; Kiyoharakogyodanchi; Kiyoharakogyodanchi Utsunomiya Japan

Elderberries Whole Organic (Natural Grocers) – Salmonella Risk (2020)

Salmonella

Potential contamination with Salmonella.

Class IIModerate

FDAOct 27, 2020AZ, AR, CO +17 more• Vitamin Cottage Natural Foods Market, Inc DBA Natural Grocers

Olanzapine ODT (Jubilant) – Subpotent Medication (2020)

Subpotent

Class IIILow

FDAOct 26, 2020Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

BD Ultra-Fine Pen Needles (Becton Dickinson) – Mislabeling (2020)

Product shelf cartons incorrectly labeled as products intended for the Latin American market. Although the product description on the label 32G x 4mm pen needles is correct, information pertinent to users in the US regarding compatibility with specific pen needles is missing.

Moderate

FDAOct 23, 2020Nationwide• Becton Dickinson & Company

Geistlich Bio-Oss Pen 1-2mm (Geistlich) – Granule Expulsion Risk (2020)

Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could suddenly drop, and the granules may be expelled all at once, causing surrounding tissue, particularly in use for the sinus lift indication and while unlikely, could pose a risk for patient harm, including irritation of the oral mucosa or even a perforation of the Schneiderian membrane

Moderate

FDAOct 19, 2020Nationwide• Geistlich Pharma North America, Inc.

MEVION S250 Radiation System (Mevion) – Treatment Beam Error (2020)

Treatment beam information disappears on Treatment Console screen while beam delivery continues potential for harm to a patient could occur

High

FDAOct 19, 2020Nationwide• Mevion Medical Systems, Inc.

Geistlich Bio-Oss Pen 0.25-1mm (Geistlich) – Granule Expulsion Risk (2020)

Moderate

FDAOct 19, 2020Nationwide• Geistlich Pharma North America, Inc.

DABRA Laser (Ra Medical) – Footswitch Protection Issue (2020)

Due to footswitch not meeting required specification for protection from ingress of solids or liquids. If spilling of liquids near or on the footswitch, it may fail in the 'on' position and allow the laser to continue to lase.

High

FDAOct 16, 2020AL, AZ, CA +13 more• Ra Medical Systems, Inc.

Cardioblate CryoFlex Probe (Medtronic) – Sterile Barrier Defect (2020)

There is a potential defect in the seals of the sterile barrier pouch used to package the CryoFlex disposables devices

Moderate

FDAOct 12, 2020Nationwide• MEDTRONIC ATS MEDICAL, INC.

Happy Tot Oat Bar Blueberries (Happy Family) – Mold Growth (2020)

Recall due to mold growth observed (Eurotium spp., Aspergillus niger, and Xeromyces bisporus).

Class IIModerate

FDAOct 12, 2020AL, AZ, AR +36 more• Nurture Inc. dba Happy Family

Happy Tot Oat Bar Bananas (Happy Family) – Mold Growth (2020)

Recall due to mold growth observed (Eurotium spp., Aspergillus niger, and Xeromyces bisporus).

Class IIModerate

FDAOct 12, 2020AL, AZ, AR +36 more• Nurture Inc. dba Happy Family

Happy Kid Fruit & Oat Bar (Happy Family) – Mold Growth (2020)

Recall due to mold growth observed (Eurotium spp., Aspergillus niger, and Xeromyces bisporus).

Class IIModerate

FDAOct 12, 2020AL, AZ, AR +36 more• Nurture Inc. dba Happy Family

CAS-930A Flat Panel Monitor (Canon) – Cable Breakage Risk (2020)

There is a potential that the cable of the Flat panel detector may break during a procedure which may cause the x-ray device to stop before the examination is completed. This could result in a delay with procedure and/or potential damage to the patients blood vessels due to removal without visibility.

Moderate

FDAOct 8, 2020Nationwide• Canon Medical System, USA, INC.

RayStation Software (RaySearch) – Import Mapping Issue (2020)

If a region of interest (ROI) or point of interest (POI) that is referenced from an imported plan is missing in the imported RT Structure Set, the reference may become linked to the wrong ROI or POI.

High

FDAOct 8, 2020Nationwide• RAYSEARCH LABORATORIES AB Sveavagen 9 Stockholm Sweden