immediate action Recalls

2,756 recalls tagged with “immediate action”.

Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Co-op Recalling 7,455 lbs of Cheese Loaves Over Listeria Contamination (

Middlefield Original Cheese Co-op is recalling 7,455 pounds of Monterey Jack and Provolone cheese loaves. The products were distributed to Ohio, Pennsylvania, Wisconsin and Texas. The recall is due to potential contamination with Listeria monocytogenes. Consumers who bought these loaves should not consume them and should contact the cooperative for refund or replacement.

Middlefield Original Cheese Cooperative
Potential contamination
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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

Claire Ellen Products Neuroquell & Neuroquell Plus Recall: 72 Containers in 2025

Claire Ellen Products recalled 72 containers of Neuroquell and Neuroquell Plus after cGMP violations were identified. The recall covers 0.22 fl oz bottles distributed online. Consumers should stop using the product immediately and contact Atlantic Management Resources Ltd. via email for guidance.

Claire Ellen Products
cGMP violations
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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Smoked Cheddar Recalled for Listeria Risk in 2025

Middlefield Original Cheese Cooperative recalled 364.125 cases of Smoked Cheddar loaves sold through multiple retailers in Ohio, Pennsylvania, Wisconsin and Texas after a Listeria monocytogenes concern. The recall is Class I and carries a high hazard. Consumers who bought 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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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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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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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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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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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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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 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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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 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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Food & Beverages
HIGH
FDA FOOD

Country Eggs Shell Egg Recall Affects 81,542 Dozen Across CA and NV

Country Eggs LLC recalled 81,542 dozen shell eggs distributed to 11 consignees in California and Nevada due to potential salmonella contamination. The recall covers Nagatoshi, Nijiya, Mizuho, and Sunshine yolk varieties sold in large AA Brown egg cartons. Consumers should not eat these eggs and should seek refund or replacement.

Country Eggs
Shell egg
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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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Vehicles & Parts
HIGH
NHTSA

Kia 2025 K4 and Sorento Recalled for Engine Fasteners SC349

Kia America, Inc. recalls 2025 K4 and Sorento vehicles at Kia dealerships after finding the connecting rod bolts may have been improperly tightened. The defect can cause a loss of drive power, increasing the risk of a crash. Owner notification letters are scheduled to be mailed September 12, 2025, and dealers will replace the sub engine assembly at no charge.

Kia
A loss
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Tag Statistics

Total Recalls
2,756

Related Tags

poisoning riskstop use immediatelyreturn for refundfda regulatedcpsc regulatedkitchengaragereplacement availablelaceration riskchemical hazardelectrical hazardoutdoor