immediate action Recalls

2,679 recalls tagged with “immediate action”.

Health & Personal Care
HIGH
FDA DRUG

ATORVASTATIN CALCIUM Tablets 10 mg Recall: 141,984 Bottles Nationwide (2025)

Ascend Laboratories, Parsippany, NJ is recalling 141,984 bottles of ATORVASTATIN CALCIUM Tablets USP, 10 mg, nationwide, manufactured by Alkem Laboratories, Ltd. in India. The issue is failed dissolution specifications, which could lead to improper dosing. Healthcare providers and patients should stop using the product and contact Ascend Laboratories for guidance.

ATORVASTATIN CALCIUM
Failed Dissolution
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Health & Personal Care
HIGH
FDA DRUG

Ascend Laboratories Recalls Alkem Atorvastatin Calcium 20 mg Tablets for Dissolution Failures (3 NDC

Ascend Laboratories recalls Alkem Atorvastatin Calcium Tablets USP 20 mg for dissolution failures in 2025. Distributed by Ascend Laboratories, Parsippany, NJ, nationwide. The issue: dissolution specifications not met. Stop use immediately and follow recall instructions. Check your NDC numbers to identify affected lots.

Ascend Laboratories
Failed Dissolution
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Health & Personal Care
HIGH
FDA DRUG

Ascend Laboratories Recall Atorvastatin Calcium 40 mg Tablets for Failed Dissolution Specifications

Ascend Laboratories recalled Atorvastatin Calcium Tablets USP 40 mg, 90-count (NDC 67877-513-90), 500-count (NDC 67877-513-05), and 1,000-count (NDC 67877-513-10) nationwide in the United States. The batches failed dissolution specifications. Patients should stop using the medication and contact Ascend Laboratories, LLC or their healthcare provider for guidance.

Atorvastatin Calcium
Failed Dissolution
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Shell Eggs Recall 2025 for Salmonella Contamination

Black Sheep Egg Company recalled Free Range Grade AA Large White Shell Eggs after Salmonella contamination concerns were identified. The recall covers 7,200 dozen eggs distributed to retail and wholesale locations in Arkansas and Missouri, with brokered sales in Mississippi, Texas, California and Indiana. Consumers should not consume these eggs and should contact the company for refund or refund/替

Black Sheep Egg Company
Potential Salmonella
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recalls 23,400 Dozen Free Range Eggs Over Salmonella Risk (2025)

Black Sheep Egg Company is recalling 23,400 dozen Free Range Grade AA Medium White Eggs sold at retail and wholesale locations in Arkansas and Missouri. The recall centers on potential Salmonella contamination. Consumers should not consume the eggs and should contact Black Sheep Egg Company for refund or replacement information.

Black Sheep Egg Company
Potential Salmonella
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls 160 DxC 500i Modules and DxI 9000 Analyzers in 2025 Recall

Beckman Coulter recalls 160 DxC 500i Clinical Analyzer Modules and the DxI 9000 Access Immunoassay Analyzer worldwide after a software anomaly could misapply manual dilution factors. The defect affects samples already in progress using the same Sample ID. Stop using the devices immediately and follow the recall instructions. Beckman Coulter will provide instructions via the recall process.

Beckman Coulter
Beckman Coulter
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recalls 16,245 Dozen Free Range Eggs (18ct) 2025

Black Sheep Egg Company recalled 16,245 dozen Free Range Grade A Large Brown Eggs sold at retail locations in Arkansas and Missouri, and through wholesale brokers in Mississippi, Texas, California and Indiana. The cartons carry UPC 860010568538. Consumers should not eat these eggs and should contact Black Sheep Egg Company for refunds or replacements.

Black Sheep Egg Company
Potential Salmonella
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Recalled IcyBreeze Buddy Portable Misting Fan in slate blue
HIGH
CPSC

IcyBreeze Recall Expands Over Fire Hazard Risk in Portable Misting Fans (2025)

IcyBreeze recalled the IcyBreeze Buddy portable misting fan due to a charging fire hazard. The recall affects consumers who own the IcyBreeze Buddy with a 1.5-liter water tank and a 10,000 mAh lithium-ion battery. Affected units must be returned for a full refund and disposal guidance. Call 817-900-2664 or visit the recall page to begin the process and receive a $150 credit at Solo Brands brands.

IcyBreeze Cooling
The misting
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Recalled Five Below Tabletop Fire Pit – smooth model
HIGH
CPSC

Five Below Recalls Tabletop Fire Pits for Risk of Serious Burn Injury

Five Below recalls two tabletop fire pits after reports of alcohol fuel flames jetting and spreading. The recall affects devices sold nationwide. Stop using the recalled pits immediately and contact Five Below for a refund. Full refunds available or $5 option; mail-back refunds possible with photo submission.

Five Below
Alcohol fuel
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Health & Personal Care
HIGH
FDA DEVICE

Cardinal Health 200 Salem Sump Gastroduodenal Tubes Recalled Worldwide for ARV Breakage

Cardinal Health 200, LLC recalled Salem Sump gastroduodenal tubes worldwide after reports of anti-reflux valve breakage. The ARV can fail under excessive force during use. Healthcare providers and patients should stop using the device immediately and follow the manufacturer instructions for recall communication.

Cardinal Health 200
Firm has
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Food & Beverages
HIGH
FDA FOOD

Kirkland Signature Ahi Tuna Wasabi Poke Recalled Over Listeria Risk

Kirkland Signature Ahi Tuna Wasabi Poke sold at Costco is recalled after a Listeria monocytogenes positive test in green onions used in the product. Western United Fish Company initiated the recall. Consumers should not eat the product and should seek refunds or replacements.

Kirkland Signature
Listeria monocytogenes.
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Tag Statistics

Total Recalls
2,679

Related Tags

stop use immediatelyreturn for refundfda regulatedadult productpoisoning riskreplacement availablecpsc regulatedkitchengarageinfant productpet relatedwinter product