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Dollar General Corporation

Dollar General Corporation Recalls

All product recalls associated with Dollar General Corporation.

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Recall Summary

Total Recalls

1000

Past Year

426

Class I (Serious)

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 221–240 of 4598 recalls

Checkers Seasoned Fries (Dollar General) – temperature abuse (2025)

Temperature abuse due to temperature excursion in one shipping trailer

Class IIModerate

FDAJul 14, 2025LA• Dollar General Corporation

Lactose Free Milk (Dollar General) – Temperature Abuse (2025)

Temperature abuse due to temperature excursion in one shipping trailer

Class IIModerate

FDAJul 14, 2025LA• Dollar General Corporation

Minute Maid Fruit Punch (Dollar General) – Temperature Abuse (2025)

Temperature abuse due to temperature excursion in one shipping trailer

Class IIModerate

1...10 111213 14...230

Page 12 of 230Next

FDA

Jul 14, 2025

• Dollar General Corporation

Twister Fruit Punch (Dollar General) – temperature abuse (2025)

Temperature abuse due to temperature excursion in one shipping trailer

Class IIModerate

FDAJul 14, 2025LA• Dollar General Corporation

Clover Valley Chocolate Milk (Dollar General) – temperature abuse (2025)

Temperature abuse due to temperature excursion in one shipping trailer

Class IIModerate

FDAJul 14, 2025LA• Dollar General Corporation

Chobani Cookie Dough Yogurt (Dollar General) – temperature abuse (2025)

Temperature abuse due to temperature excursion in one shipping trailer

Class IIModerate

FDAJul 14, 2025LA• Dollar General Corporation

NH European Style Butter Blend (Bunge) – undeclared milk (2025)

Undeclared Allergen

allergen labeling - undeclared milk

Class IIModerate

FDAJul 14, 2025IN• BUNGE NORTH AMERICA INC

Bontrager 7ROD (Bontrager Outdoors) – Carbon Monoxide Detection (2025)

Bontrager Outdoors (Bontrager) is recalling certain 2025 Skinny Guy Campers Armor 7LT and Bontrager Outdoors 7ROD trailers. The carbon monoxide detectors may not have been installed.

Moderate

NHTSAJul 8, 2025Nationwide• BONTRAGER OUTDOORS

GE OEC 9800 (GE Medical Systems) – Regulatory Non-Conformance (2025)

GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.

Moderate

FDAJul 2, 2025Nationwide• GE Medical Systems, LLC

GE OEC 9900 Elite C-arm Systems (GE Medical Systems) – Non-Conformance (2025)

Moderate

FDAJul 2, 2025Nationwide• GE Medical Systems, LLC

Peripheral Parenteral Nutrition (CAPS) – Processing Controls (2025)

Lack of Processing Controls; prescriptions were compounded in an ISO-5 area where it was identified that a daily cleaning step was not sufficiently documented.

Class IIModerate

FDAJul 1, 2025CA• Central Admixture Pharmacy Services, Inc (CAPS) Los Angeles

Atlas Cross Sport (VOLKSWAGEN) – Brake Bolt Issue (2025)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2023-2025 Atlas, Atlas Cross Sport and 2023-2024 ID.4 vehicles. Certain bolts on the chassis, brake system and/or suspension (such as bolts for certain cross member, engine mount, control arm, subframe, rear brake carrier, etc.) of affected vehicles may not have been correctly tightened during the manufacturing process.

Moderate

NHTSAJun 30, 2025Nationwide• VOLKSWAGEN

Duloxetine Capsules (Breckenridge) – CGMP Impurity (2025)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

Class IIModerate

FDAJun 30, 2025Nationwide• Breckenridge Pharmaceutical, Inc.

Sprinter Cart Infusion Pole (Maquet) – Labeling Requirement (2025)

Device does not comply with the labeling requirements of international standard IEC 60601-1.

Low

FDAJun 27, 2025Nationwide• Maquet Cardiopulmonary Gmbh Kehler Str. 31 Rastatt Germany

Injection Needle (Spiggle & Theis) – Cytotoxicity Risk (2025)

Affected product show elevated cytotoxicity values. Use of affected injection needles may present a risk of intolerance reaction or allergic reaction.

Moderate

FDAJun 27, 2025Nationwide• Spiggle & Theis Mt Gmbh Lagerstr. 11 Dieburg Germany

Orange EV Husk-E (ORANGE EV) – Fastener Problem (2025)

Fire/Burn Risk

Orange EV (OEV) is recalling certain 2023-2025 HUSK-e terminal trucks previously remedied under Recall 25V367 (2025-SRC-04). The wrong size washer was installed in the thermal fuse bolted joint during the previous repair.

Very High

NHTSAJun 27, 2025Nationwide• ORANGE EV

GEM ELXD (GEM) – Ball Joint Fastener (2025)

GEM WAEV LLC (GEM) is recalling certain 2022-2025 e2, e4, e6, and eLXD vehicles. The retaining fasteners between the ball joint and the hub strut may have been improperly tightened, which can result in ball joint separation from the wheel.

High

NHTSAJun 23, 2025Nationwide• GEM

Signa Voyager (GE Medical) – MR System Concern (2025)

GE HealthCare has become aware that for certain MR systems (SIGNA Artist, SIGNA Voyager, Discovery MR450 1.5T, Optima MR450w 1.5T, SIGNA Architect, SIGNA Premier, SIGNA UHP, Discovery MR750 3.0T, Discovery MR750w 3.0T, SIGNA Hero, SIGNA PET/MR, SIGNA Artist Evo, SIGNA Voyager AIR (China Only), SIGNA Architect AIR (China Only), SIGNA Premier XT (China Only), SIGNA Premier Elite (China Only), SIGNA Premier MAX (China Only), SIGNA Hero XT (China Only), SIGNA Hero Elite (China Only), SIGNA Hero MAX (China Only), SIGNA PET/MR AIR (China Only), SIGNA PET/MR AIR Plus (China Only), the planned maintenance steps to check the functionality of the caster locks on the MR patient table may not have been performed.

Moderate

FDAJun 20, 2025Nationwide• GE Medical Systems, LLC

Signa Artist (GE Medical) – MR System Concern (2025)

Moderate

FDAJun 20, 2025Nationwide• GE Medical Systems, LLC

GE SIGNA PET/MR AIR (GE Medical Systems) – China MRI Concern (2025)

Moderate

FDAJun 20, 2025Nationwide• GE Medical Systems, LLC