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Grimmway Enterprises, Inc. dba Grimmway Farms

Grimmway Enterprises, Inc. dba Grimmway Farms Recalls

All product recalls associated with Grimmway Enterprises, Inc. dba Grimmway Farms.

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Recall Summary

Total Recalls

1000

Past Year

891

Class I (Serious)

124

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 4901–4920 of 17593 recalls

Organic Petite Carrots (Grimmway Farms) – Salmonella Contamination (2021)

Salmonella

Carrot products may be contaminated with Salmonella

Class IHigh

FDAJul 19, 2021Nationwide• Grimmway Enterprises, Inc. dba Grimmway Farms

Shredded Carrots (Grimmway Farms) – Salmonella Contamination (2021)

Salmonella

Carrot products may be contaminated with Salmonella

Class IHigh

FDAJul 19, 2021Nationwide• Grimmway Enterprises, Inc. dba Grimmway Farms

Backcountry Dried Apricots (Lipari Foods) – Undisclosed Sulfites (2021)

1...244 245246247 248...880

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Sulfites not disclosed on labeling

Class IHigh

FDAJul 16, 2021AL, FL, GA +15 more• Lipari Foods Operating Company, LLC.

Normand Remisol Data Manager (Beckman Coulter) – Patient Result Error (2021)

There is a potential that the data management system may add additional cells to the patient request which could lead to erroneous patient result.

Moderate

FDAJul 15, 2021Nationwide• Beckman Coulter Inc.

Cell Marque PSA Antibody (Cell Marque) – Expiration Date Mismatch (2021)

Mouse Monoclonal Antibody labelled with an incorrect expiry date of 31 Dec 2023. The correct expiry date is 31 Dec 2022. If used beyond expiry, the material performance is likely to decrease and may be observed as weak or no staining, and there is a potential risk that a false negative result could be recorded and may lead to delay of diagnosis due to retest.

Moderate

FDAJul 15, 2021Nationwide• Cell Marque Corporation

Continental MKC1 Brake Unit (Continental) – Brake System Risk (2021)

Continental Automotive Systems, Inc. (Continental Automotive) is recalling certain Hydraulic Electronic MKC1 brake units, with part numbers 10-1202 and 25-1202. A deviation in the welding process can cause the Anti-Lock Brake System (ABS) Hydraulic Control Unit (HCU) rotor and shaft to separate, which may cause a reduction of braking assist, and a loss of ABS.

High

NHTSAJul 15, 2021Nationwide• CONTINENTAL AUTOMOTIVE

Heater Cooler Unit (Maquet) – Contamination Risk (2021)

There is the potential for contaminated water to enter parts of the Heater-Cooler Unit circuits. There is a potential risk of bacterial contamination including Mycobacteria species.

High

FDAJul 14, 2021AL, CA, FL +7 more• Maquet Medical Systems USA

Neutrogena Beach Defense Sunscreen (Johnson & Johnson) – Manufacturing Deviation (2021)

cGMP Deviations

Class IIModerate

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.

Neutrogena COOLDRY SPORT Micromesh Sunscreen (Johnson & Johnson) – Manufacturing Deviation (2021)

cGMP Deviations

Class IIModerate

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.

Neutrogena Beach Defense Sunscreen (Johnson & Johnson) – Manufacturing Deviation (2021)

cGMP Deviations

Class IIModerate

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.

Neutrogena COOLDRY SPORT Sunscreen (Johnson & Johnson) – Manufacturing Deviation (2021)

cGMP Deviations

Class IIModerate

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.

Neutrogena Invisible Daily Defense Sunscreen (Johnson & Johnson) – Manufacturing Deviation (2021)

cGMP Deviations

Class IIModerate

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.

Neutrogena Ultra Sheer Body Mist SPF 30 Sunscreen (Johnson & Johnson) – Manufacturing Deviation (...

cGMP Deviations

Class IIModerate

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.

Neutrogena COOLDRY SPORT SPF 100 Sunscreen (Johnson & Johnson) – Manufacturing Deviation (2021)

cGMP Deviations

Class IIModerate

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.

Neutrogena Beach Defense Sunscreen Spray (Johnson & Johnson) – Manufacturing Deviation (2021)

cGMP Deviations

Class IIModerate

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.

Neutrogena Beach Defense Sunscreen (Johnson & Johnson) – Manufacturing Deviation (2021)

cGMP Deviations

Class IIModerate

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.

Neutrogena Ultra Sheer Body Mist Sunscreen (Johnson & Johnson) – Manufacturing Deviation (2021)

cGMP Deviations

Class IIModerate

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.

BHR Square Headed Nail (Smith & Nephew) – Nail Head Detachment (2021)

The nail head may become detached during surgery.

High

FDAJul 14, 2021Nationwide• Smith & Nephew Orthopaedics Ltd. (Aurora) Aurora, Spa Park Harrison Way Leamington Spa United Kingdom

Neutrogena Beach Defense Sunscreen (Johnson & Johnson) – Manufacturing Deviation (2021)

cGMP Deviations

Class IIModerate

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.

Neutrogena Beach Defense Sunscreen (Johnson & Johnson) – Benzene Contamination (2021)

Chemical Contamination: presence of benzene

Class IHigh

FDAJul 14, 2021Nationwide• Johnson & Johnson Consumer, Inc.