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Michael Foods, Inc.

Michael Foods, Inc. Recalls

All product recalls associated with Michael Foods, Inc..

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Recall Summary

Total Recalls

1000

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 1841–1860 of 2399 recalls

Frozen Egg Patties (Michael Foods) – undeclared milk (2015)

Improperly declared milk allergen.

Class IIModerate

FDAFeb 13, 2015Nationwide• Michael Foods, Inc.

Milk Chocolate Royal Icing Pops (Chocolate By Design) – undeclared allergens (2015)

Undeclared Egg

The products contain undeclared egg and FD&C colors Yellow 5 or 6, Red 3 or 40, and/or Blue 1 from the royal icing component used on the finished pops.

Class IHigh

FDAFeb 12, 2015NJ, NY, VA• Chocolate By Design, Inc.

Golden Smoked Herring (Moscahlades Bros) – botulinum risk (2015)

Smoked herring may be potentially contaminated with C. botulinum.

Class I

1...91 929394 95...120

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High

FDAFeb 11, 2015IL, MD, MA +4 more• Moscahlades Bros Inc

Ground Cumin (E & S) – peanut protein contamination (2015)

Colonna Brothers is recalling ground cumin received from its supplier that may be contaminated with peanut proteins.

Class IHigh

FDAJan 26, 2015NJ, NY, PA• Colonna Brothers Inc.

Cremosa Ground Cumin (Colonna Brothers) – Peanut Protein Contamination (2015)

Colonna Brothers is recalling ground cumin received from its supplier that may be contaminated with peanut proteins.

Class IHigh

FDAJan 26, 2015NJ, NY, PA• Colonna Brothers Inc.

Price Rite Ground Cumin (Colonna Brothers) – Peanut Protein Risk (2015)

Colonna Brothers is recalling ground cumin received from its supplier that may be contaminated with peanut proteins.

Class IHigh

FDAJan 26, 2015NJ, NY, PA• Colonna Brothers Inc.

Raw Milk Cheddar Cheese (Farm Country) – Listeria Contamination (2014)

Listeria

Product may be contaminated with Listeria monocytogenes

Class IHigh

FDADec 23, 2014MI• Farm Country Cheese House, Inc.

Fresenius Medical Care Holdings, Inc.: Fresenius Crit Line in a Clip (CLiC) with SW version 2.51...

Potential for misinterpretation of the graphic display of the Blood Volume ( BV) slope

Class IIModerate

FDADec 19, 2014CT, NY• Fresenius Medical Care Holdings, Inc.

Circuit Breakers (Schneider Electric) – electrical safety (2014)

Fire/Burn Risk

The recall involves PowerPact J-frame molded case circuit breakers with thermal-magnetic trip units. The circuit breakers are made of black plastic and have a three-position breaker handle that indicates whether the breaker is off, on or tripped. The recalled circuit breakers are rated for 150 to 250 amps, have interruption ratings of D, G, J, L and R. They were manufactured in two pole and three pole configurations with either lug-in/lug-out or plug-in (I-Line) style connectors. Brand name "Schneider Electric" or "Square D" is on a yellow sticker above the breaker handle and on the top of a label on the side of the circuit breaker. A label on the front of the circuit breaker to the left of the breaker handle has the catalog number at the top. The number also appears on a label on the side of the breaker. Schneider Electric catalog numbers begin with "NJ" and Square D catalog numbers begin with "J." A label on the front of the circuit breaker to the right of the breaker handle has the date code in the lower right corner. Recalled circuit breakers were manufactured from March 26, 2014 through September 26, 2014 and have date codes 14131 through 14395. The date codes are in the YYWWD format (example: 14131 = year 2014, week 13, day of the work week 1/ Monday). Breakers with following catalog numbers are being recalled: Catalog Number Breaker Type (N)JDX26XXX 2 Pole (N)JGX26XXX 2 Pole (N)JJX26XXX 2 Pole (N)JLX26XXX 2 Pole (N)JDX36XXX 3 Pole (N)JGX36XXX 3 Pole (N)JJX36XXX 3 Pole (N)JLX36XXX 3 Pole (N)JRX36XXX 3 Pole

CPSCDec 18, 2014Nationwide• Schneider Electric USA Inc., of Columbia, Mo., and Tlaxcala, Mexico

Roche Diagnostics Operations, Inc.: Cobas b 221 (versions 5 and 6) Blood Gas and Electrolytes...

Chemical component of the F3 Fluid pack and environmental bacterial contamination causes a positive bias up to 39% at 4.1 mmol/l for the glucose measurement and 30% at 4.12 mmol/l for lactate. Urea readings are unaffected.

Class IIModerate

FDADec 18, 2014Nationwide• Roche Diagnostics Operations, Inc.

Roche Molecular Systems, Inc.: cobas 4800 KRAS AMP/DET 24T CE-IVD Mutation Test; CE-IVD ...

cobas KRAS Mutation Kit T10786 is generating invalid results for the Mutant Control and/or KRAS Calibrator.

Class IIILow

FDADec 18, 2014Nationwide• Roche Molecular Systems, Inc.