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Krinos Foods, Inc.

Krinos Foods, Inc. Recalls

All product recalls associated with Krinos Foods, Inc..

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Recall Summary

Total Recalls

970

Past Year

Class I (Serious)

Most Recent

Nov 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 601–620 of 970 recalls

Krinos Tahini Sesame Seeds (Krinos) – salmonella risk (2013)

Salmonella

Salmonella contamination.

Class IHigh

FDAApr 26, 2013CA, CO, CT +20 more• Krinos Foods, Inc.

Isovue-370 Injection (Bracco) – particulate matter (2012)

Presence of Particulate Matter; fibers identified as cellulose and polyvinyl

Class IHigh

FDANov 21, 2012Nationwide• Bracco Diagnostic Inc

Isovue-300 Injection (Bracco) – particulate matter (2012)

Presence of Particulate Matter; fibers identified as cellulose and polyvinyl

Class I

1...29 303132 33...49

Page 31 of 49Next

High

FDANov 21, 2012Nationwide• Bracco Diagnostic Inc

Choletec Kit (Bracco) – Particulate Matter Risk (2012)

Presence of Particulate Matter; potential for charcoal particulates

Class IIILow

FDAAug 14, 2012Nationwide• Bracco Diagnostic Inc

Cardiogen-82 (Bracco Diagnostics) – Sr-82 level deviation (2012)

GMP deviation; Sr-82 levels exceeded alert limit specification

Class IIModerate

FDAJun 1, 2012Nationwide• Bracco Diagnostics Inc

Organic Paprika (Brinkhoff & Monoson) – unapproved colors (2012)

Organic Paprika contains unapproved colors.

Class IIModerate

FDAMay 11, 2012Nationwide• Brinkhoff & Monoson Inc

Multihance Injection (Bracco) – Sterility Concern (2012)

Lack of Assurance of Sterility; Product recalled due to displacement of the aluminum crimp cap during product usage.

Class IIModerate

FDAApr 16, 2012Nationwide• Bracco Diagnostics Inc

Multihance Injection (Bracco) – Short Fill Potential (2012)

Short Fill: The product is being recalled due to a potential underfill of the affected vials.

Class IIILow

FDAApr 16, 2012Nationwide• Bracco Diagnostics Inc

Abbott Diagnostics International, Ltd. Carr # 2 Km 58.0 Cruce Davila: ARCHITECT HAVAB-M Reagent A chemiluminescent micropartic...

There is a potential to generate a false grayzone or reactive HAVAB-M result when the ARCHITECT AUSAB assay precedes the ARCHITECT HAVAB-M assay.

FDADec 30, 2009Nationwide• Abbott Diagnostics International, Ltd. Carr # 2 Km 58.0 Cruce Davila

Siemens Healthcare Diagnostics, Inc.: Dimension IBCT Flex Reagent Cartridge. The total (IBCT) m...

Test produces falsely elevated IBCT results and Abnormal Reaction test report messages on heparinized plasma samples.

FDADec 16, 2009Nationwide• Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc.: Stratus(R) CS Rotors, catalog number CROTOR, lot number N...

Low frequency defect in the gel filling of this lot that may result in inadequate separation of cells in centrifugation.

FDADec 7, 2009AK, AZ, AR +25 more• Siemens Healthcare Diagnostics, Inc.

Vital Diagnostics, Inc.: ATAC Serum Control Kit. The device is used for monitorin...

Vital Diagnostics observed a bias in the Quality Control Consensus Program between published values for ALP on the ATAC 8000 and reported customer means. The ranges were adjusted to reflect the analyzer population.

FDADec 4, 2009Nationwide• Vital Diagnostics, Inc.

Vital Diagnostics, Inc.: Envoy 500 Serum Control Kit. The device is used for moni...

FDADec 4, 2009Nationwide• Vital Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc.: Dimension Vista LOCI Reaction Vessel

Some vessels may leak. If leakage occurs, patient results will be flagged and are not reportable.

FDANov 24, 2009CA, CO, FL +18 more• Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics Inc: RapidPoint 405 System Analyzers The RP405 is capable of ...

Software: Reference sensor failure may result in inaccurate pH reuslts

FDAOct 30, 2009PR• Siemens Healthcare Diagnostics Inc

Siemens Healthcare Diagnostics Inc: RapidPoint 400 Analyzers for Blood Gas, Electrolytes and ...

Software: Reference sensor failure may result in inaccurate pH reuslts

FDAOct 30, 2009PR• Siemens Healthcare Diagnostics Inc

Inova Diagnostics Incorporated: Inova Diagnostics BINDAZYME Human C1q binding Circulating...

The recall was initiated after the binding site notified Inova Diagnostics, inc. that the affected Bindazyme Human C1q binding Circulating Immune Complex EIA Kits may contain an ELISA plate labeled as "tissue Transglutaminase Coated Wells" instead of "C1q Coated Wells".

FDAOct 28, 2009Nationwide• Inova Diagnostics Incorporated

Siemens Healthcare Diagnostics, Inc.: Dimension Vista CHEM 3 calibrator is an in vitro diagnos...

patient results are depressed

FDAOct 23, 2009Nationwide• Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc.: Dimension Vista V-LYTE Fluids: Standard A catalog number ...

Results can elevate after sensor replacement. Sodium urine results can be falsely elevated 15 mmol/L within 24 hours after installation of a new sensor.

FDAOct 22, 2009Nationwide• Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc.: Dimension Vista V-LYTE Fluids: Standard B/Salt Bridge cat...

Results can elevate after sensor replacement. Sodium urine results can be falsely elevated 15 mmol/L within 24 hours after installation of a new sensor.

FDAOct 22, 2009Nationwide• Siemens Healthcare Diagnostics, Inc.