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Great Lakes Cheese Co Inc

Great Lakes Cheese Co Inc Recalls

All product recalls associated with Great Lakes Cheese Co Inc.

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Recall Summary

Total Recalls

1000

Past Year

726

Class I (Serious)

175

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 4081–4100 of 11124 recalls

American Cheese Yellow (Great Lakes Cheese) – metal contamination (2019)

5 lb. loaves of cheese may contain metal foreign material.

Class IIILow

FDAOct 11, 2019FL, GA, IL +9 more• Great Lakes Cheese Co Inc

Encina HA Femoral Stem (Signature Orthopaedics) – mislabeled packaging (2019)

The firm has identified that packaging containing components of the hip replacement range are mislabeled. This could result in the product intended to be used for a procedure not included in the packaging resulting in a surgical delay.

Low

FDAOct 9, 2019CA• Signature Orthopaedics Europe Ltd Unit A, IDA Business & Technology Park Garrycastle Athlone Ireland

Zimmer Tourniquet Cuff (Stryker) – mislabeling risk (2019)

Tourniquet cuffs are potentially mislabeled. If used may lead to (1) Device misuse during procedure (2) Inadequate Limb Compression Force.

Low

1...203 204205206 207...557

Page 205 of 557Next

FDA

Oct 9, 2019

Nationwide

• Stryker Sustainability Solutions

Lawn Mower Engines (Kawasaki) – Fire Hazard (2019)

Fire/Burn Risk

This recall involves Kawasaki engines used in riding lawn mowers sold under the Ferris brand name with mower model number IS ® 2100Z ZTR and the Cub Cadet Pro Z 760 LKW EFI . The recalled engines are model year 2017 and 2018 Kawasaki FX850V-EFI series, including models FX850V-AS44 with serial number range FX850VB19736-FX850VB44147 and FX850V-AS47 with serial number range FX850VB20733-FX850VB40776. "Kawasaki FX850V EFI" is printed on the engine fan housing. The engine model and serial number are located on the engine fan housing.

High

CPSCOct 8, 2019Nationwide• Kawasaki Motors Manufacturing Corp. U.S.A., of Maryville, Mo.

UniCel DxH Slidemaker (Beckman Coulter) – cell carryover risk (2019)

When the UniCel DxH Slidemaker Stainer and UniCel DxH Slidemaker Stainer II dispense probe is slightly bent, there is a potential for cell carryover from the previous sample, and erroneous results could be reported from the slide review. Erroneous results may be reported from the laboratory which may trigger unnecessary or inappropriate patient treatment.

Moderate

FDAOct 7, 2019Nationwide• Beckman Coulter, Inc.

Liquid Cardiac Controls (Randox) – N-proBNP Recovery Issue (2019)

Removal of claims for N-proBNP in the Liquid Cardiac Control model numbers CQ5051 due to an observed decrease in recovery for N-Terminal Pro-Brain Natriuretic Peptide (NT-proBNP) in recent lots.

Moderate

FDAOct 4, 2019CA, CO, DE +7 more• Randox Laboratories, Limited Ardmore; 55 The Diamond Road Crumlin United Kingdom

Methylphenidate HCl Oral Solution (KVK-Tech) – Foreign Substance (2019)

Presence of Foreign Substance; Fiber particles.

Class IIILow

FDAOct 4, 2019Nationwide• KVK-Tech, Inc.

Guardia Access Nano Embryo Catheter (Cook) – Bent Tip Issue (2019)

Bent transfer catheter tips may cause difficulty or inability in inserting the transfer catheter into the guiding catheter. Potential adverse events that may occur if an affected product is used include increased procedural time, the need for a repeat embryo transfer procedure, or the need for a patient to undergo an additional IVF cycle.

Moderate

FDAOct 3, 2019Nationwide• Cook Inc.

Guardia Access Embryo Catheter (Cook) – Bent Tip Issue (2019)

Moderate

FDAOct 3, 2019Nationwide• Cook Inc.

Climax Spring Water (King Bottling) – Bromate Excess (2019)

The bottled water contains bromate levels in excess of the 0.010 mg/L FDA standard of quality limit.

Class IIILow

FDAOct 3, 2019KY• King Bottling, Inc.

Jack Daniels Tennessee Whiskey Cake - Pecan (Great Spirits) – Mold Risk (2019)

Cakes are potentially moldy prior to their "best by" date.

Class IIILow

FDAOct 2, 2019CA, IN, NJ +4 more• The Great Spirits Baking Company, LLC

Jack Daniels Tennessee Whiskey Cake - Vanilla (Great Spirits) – Mold Risk (2019)

Cakes are potentially moldy prior to their "best by" date.

Class IIILow

FDAOct 2, 2019CA, IN, NJ +4 more• The Great Spirits Baking Company, LLC

Jack Daniels Tennessee Whiskey Cake - Chocolate (Great Spirits) – Mold Risk (2019)

Cakes are potentially moldy prior to their "best by" date.

Class IIILow

FDAOct 2, 2019CA, IN, NJ +4 more• The Great Spirits Baking Company, LLC

Jansal Valley Energize Snack Mix (Sid Wainer) – Incorrect Ingredients (2019)

Products were labeled with incorrect ingredient listing. The ingredients listed on the label include multiple allergens (almonds, cashews, coconut, hazelnuts, pecans, walnuts, peanuts). Label lists allergens that are not actually in the product. Allergens actually present in the product are: peanuts, almonds, cashews, coconut, hazelnuts, walnuts.

Class IIModerate

FDAOct 1, 2019CT, FL, IN +7 more• Friendly Fruit Market dba Sid Wainer & Son

Jansal Valley Indulgent Snack Mix (Sid Wainer) – Incorrect Ingredients (2019)

Products were labeled with incorrect ingredient listing. The ingredients listed on the label include multiple allergens (almonds, cashews, coconut, hazelnuts, peacans, walnuts, cashews, soy). Label lists allergens that are not actually in the product. Allergens actually present in the product are: almonds, cashews and soy.

Class IIModerate

FDAOct 1, 2019CT, FL, IN +7 more• Friendly Fruit Market dba Sid Wainer & Son

Golden Dragon Almond Cookies (Golden Dragon) – Undeclared milk (2019)

Undeclared Milk

undeclared milk

Class IHigh

FDAOct 1, 2019IL• Golden Dragon Fortune Cookies Co Inc

Cougar (Keystone) – Electrical Wiring Issue (2019)

Fire/Burn Risk

Keystone RV Company (Keystone) is recalling certain 2020 Cougar fifth wheels and travel trailers, models 22RBS, 23MLS, 25RES, 26RBS, 26RKS, 27RES, 27SAB, 27SGS, 29BHS, 29FKD, 29RLD, 30RKD, 31MBS, 32RDB, 32RLI and 34TSB. The wiring for the solar preparation kit may have been incorrectly wired to the wrong side of the 12V breaker, potentially allowing an electrical short circuit in the event of damage to the wiring.

High

NHTSASep 30, 2019Nationwide• KEYSTONE

Vivitrol (Alkermes) – incorrect needle packaging (2019)

Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch needles being placed in the 1 1/2 inch needle cardboard sleeve labelled as administration needles. The product vial is not impacted.

Class IIModerate

FDASep 26, 2019Nationwide• Alkermes, Inc.

Tiguan (Volkswagen) – Unspecified Issue (2019)

Fire/Burn Risk

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2017 Volkswagen Passat, 2018 Tiguan LWB, 2007-2009 Jetta Sedan, 2011-2013, 2015 and 2019 Jetta, 2013 Jetta Hybrid, 2008-2009 Jetta Sportwagen, 2015 Golf Sportwagen, 2013 Golf, 2008-2010 and 2012-2013 Beetle and Beetle Convertible, 2008-2010 Beetle, and Beetle Convertible vehicles. Modifications made while the vehicles were in an internal evaluation period may cause the affected vehicles to not comply with all of the applicable regulatory requirements.

High

NHTSASep 25, 2019Nationwide• VOLKSWAGEN

Dark Chocolate Gummy Bears (Newark Nut Store) – Packaging Concern (2019)

Kopper s Chocolate has initiated recall of Koppers Chocolate Dark Chocolate Gummy Bears, 4oz (113g) retail package, metallized foil resealable pouch, 12 pouches per case, printed BB: 08/2020 because the product packaging only identifies soy as an allergen. The product does not list milk , which is an allergen .

Class IIModerate

FDASep 25, 2019NJ, NY, PA• The Newark Nut Store