All Product Recalls

Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Swiss Cheese Recall for Listeria Contamination (2025)

Middlefield Original Cheese Cooperative recalls 7,455 pounds of Original Swiss Cheese distributed in Ohio, Pennsylvania, Wisconsin and Texas after potential Listeria monocytogenes contamination. The recall affects 5‑lb loaves and 2‑lb deli bags in various packaging. Consumers should not eat this cheese and should contact the cooperative for refund or replacement information.

Middlefield Original Cheese Cooperative
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Sunrise Creamery Dilly Pickle Monterey Jack Cheese Recalled Over Listeria Risk (2025) by Middlefield

Sunrise Creamery Monterey Jack Cheese with Dill Pickles is recalled by Middlefield Original Cheese Cooperative after FDA findings indicate potential Listeria monocytogenes contamination. The recall covers two SKUs in 6 oz and 1.25 lb sizes, distributed to Ohio, Pennsylvania, Wisconsin and Texas. Consumers should discard affected cheese and contact the cooperative for refund or replacement.

Sunrise Creamery
Potential contamination
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Health & Personal Care
HIGH
FDA DRUG

873 Cartons of Chlorpromazine Hydrochloride Tablets Recalled Due to Foreign Substance Risk

American Health Packaging recalled 873 cartons of Chlorpromazine Hydrochloride Tablets, USP, 200 mg, after foreign substances were detected in product packaging. A specific lot of auxiliary polyester coil contained a micro-organism, posing a high health risk. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

Chlorpromazine Hydrochloride
Presence of
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Food & Beverages
HIGH
FDA FOOD

Middlefield Organic Gouda Cheese Recall: 364 Cases Over Listeria Contamination (2025)

Middlefield Original Cheese Cooperative is recalling 364 cases of Organic Gouda Cheese, 8 oz, packaged 12 per case and distributed in Ohio, Pennsylvania, Wisconsin and Texas, after potential contamination with Listeria monocytogenes. The product poses a high risk of serious illness if consumed. Consumers should not eat the cheese and should contact the cooperative for a refund or replacement.

Middlefield Original Cheese Cooperative
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Recalls 7,455 lbs Shredded Mozzarella/Provolone (5-lb Bags)

Middlefield Original Cheese Cooperative recalled 364.125 cases of shredded Mozzarella/Provolone cheese sold in Ohio, Pennsylvania, Wisconsin, and Texas. The recall is due to potential contamination with Listeria monocytogenes. Consumers who purchased this product should not consume it and should contact the cooperative for refund or replacement information.

Middlefield Original Cheese Cooperative
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Recalls 364 Cases of Cheddar Cheese Over Listeria (2025)

Middlefield Original Cheese Cooperative recalled 364.125 cases (7,455 pounds) of All Natural Mild Cheddar Cheese and Shredded Cheddar Cheese sold at retailers in Ohio, Pennsylvania, Wisconsin and Texas. Listeria monocytogenes contamination is the stated hazard. Consumers should not consume the cheese and should contact the cooperative for a refund or replacement.

Middlefield Original Cheese Cooperative
Potential contamination
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Health & Personal Care
HIGH
FDA DRUG

Chlorpromazine Hydrochloride Tablets Recalled Nationwide for Foreign Substance in Packaging Lot 1022

A high-severity recall covers chlorpromazine hydrochloride tablets distributed nationwide by American Health Packaging. A foreign substance linked to a polyester coil packaging component was detected at the manufacturing site. No tablets were contaminated. Stop using the product and contact the distributor for guidance.

CHLORPROMAZINE HYDROCHLORIDE
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Zydus Lifesciences Succinylcholine Chloride Injection Recall Active for Unknown Impurity Degradation

Zydus Lifesciences recall remains active for 270,125 vials distributed across MS, OH, LA and Puerto Rico. The FDA notice cites failed impurities and degradation specifications as the reason. Immediate discontinuation is advised for healthcare providers and patients with ongoing prescriptions. Contact Zydus Pharmaceuticals USA Inc for guidance.

Zydus Lifesciences
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DRUG

Chlorpromazine Hydrochloride 25 mg Tablets Recalled Nationwide Over Foreign Substance in Packaging

A recall of chlorpromazine hydrochloride tablets is active nationwide in the United States. A specific lot of packaging material to coils used in manufacturing contained a foreign substance with a microorganism detected. Tablets themselves tested negative for microorganisms. Consumers and healthcare providers should stop using the product immediately and contact Amerisource Health Services LLC or

CHLORPROMAZINE HYDROCHLORIDE
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Chlorpromazine Hydrochloride Tablets Recalled Over Foreign Substance Found in Packaging Coil (High-R

Chlorpromazine Hydrochloride tablets distributed nationwide by American Health Packaging are recalled after a polyester coil used in packaging showed presence of a micro-organism in a specific lot. No tablets were contaminated. Consumers and healthcare providers should stop using this product immediately and contact Amerisource Health Services LLC for guidance.

Chlorpromazine Hydrochloride
Presence of
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Health & Personal Care
HIGH
FDA DEVICE

Vision RT Recalls AlignRT InBore System Over Laser Omission Hazard

Vision RT recalled 56 AlignRT InBore systems on August 27, 2025, due to missing safety information in the Instructions for Use. The omission pertains to the identification and characteristics of the system's Class 1 lasers as required by federal regulations. Users must stop using the device immediately and follow manufacturer instructions.

Vision RT
Vision RT
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Food & Beverages
HIGH
FDA FOOD

Extract Labs Mai Tai 20mg Gummies Recalled for Peanut Cross-Contact Risk (2025)

Extract Labs recalled 19,750 Mai Tai 20mg Gummies distributed across the United States, Australia, Germany, the United Kingdom, Malaysia and New Zealand. The unlabeled bulk product was shipped in poly gusset bags inside brown corrugated boxes with no consumer label. Consumers who bought it should not consume the product and should email Extract Labs to request a refund or replacement.

Extract Labs
Potential peanut
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Food & Beverages
HIGH
FDA FOOD

Extract Labs CBD Gummies Recalled for Peanut Cross-Contact (2,180 units, 2025)

Extract Labs recalled 2,180 sugar-free Mixed Berry CBD gummies sold through retailers nationwide in the United States and overseas after peanut protein cross-contact was detected. The product contains 10 mg CBD and 10 mg D9 THC per gummy. Consumers should stop using the product immediately and contact Extract Labs for refunds or replacements.

Extract Labs
Potential peanut
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Food & Beverages
HIGH
FDA FOOD

Extract Labs Elderberry 20mg CBD Gummies Recalled for Peanut Cross-Contact Risk (19,720 Units) 2025

Extract Labs recalled 19,720 unlabeled elderberry CBD gummies sold through private-label consignee channels in the United States and internationally. The product contains 20 mg CBD and 20 mg D9 THC per gummy and is shipped in bulk packaging with no consumer labeling. Consumers who purchased this product should not consume it and should contact Extract Labs for refund or replacement.

Extract Labs
Potential peanut
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Vehicles & Parts
HIGH
NHTSA

Hyundai Recalls 2025-2026 Santa Fe and Tucson for Engine Fastener Issue

Hyundai Motor America is recalling certain 2025-2026 Tucson and Santa Fe vehicles. The connecting rod bolts may have been improperly tightened, which can cause a loss of drive power and engine damage, potentially resulting in an oil leak. Owner notification letters are expected to be mailed October 24, 2025, and dealers will replace the engine free of charge.

Hyundai
A loss
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Food & Beverages
HIGH
FDA FOOD

Extract Labs Blue Razz 20mg CBD/THC Gummies Recall 2025 for Peanut Cross-Contact — 19,810 Units

Extract Labs recalled 19,810 Blue Razz 20mg CBD/THC gummies distributed across the United States and Australia, as well as Germany, the United Kingdom, Malaysia and New Zealand. The unlabelled bulk product was shipped in poly gusset bags inside brown boxes. Consumers who may have peanut allergies should not consume the product; contact Extract Labs for a refund or replacement via email.

Extract Labs
Potential peanut
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Health & Personal Care
HIGH
FDA DRUG

B. Braun Medical 3000 mL Saline Irrigation Bags Recalled for Sterility Concerns

B. Braun Medical Inc. recalled 16,228 3000 mL saline irrigation bags nationwide in the United States. The recall cites lack of assurance of sterility due to port misalignment, creating a potential for fluid leakage. Healthcare providers and patients should stop using the product immediately and contact the company for guidance.

B. Braun Medical Inc.
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

GORE ACUSEAL Vascular Graft Recall Affects 52,306 Devices Worldwide (2025)

Gore recalled 52,306 Gore ACUSEAL Vascular Grafts distributed through healthcare providers in the United States and internationally after reports of graft delamination. Delamination may reduce access flow, cause cannulation difficulties, bleeding or bruising, and may require reinterventions. Healthcare facilities and patients should stop using the device immediately and follow the recall guidance.

Gore
Reports of
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