replacement available Recalls

1,215 recalls tagged with “replacement available”.

Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recalled 14,220 Dozen Free Range Eggs Over Salmonella Risk (2025)

Black Sheep Egg Company recalled 14,220 dozen Free Range Grade AA Medium Brown Eggs after FDA notice of potential Salmonella contamination. The recall covers loose-pack boxes sold at retail and wholesale locations in Arkansas and Missouri, with wholesale distribution to Mississippi, Texas, California and Indiana. Consumers should not consume the eggs and should contact the company for refunds or替换

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

Black Sheep Egg Company Recall: 288,900 Dozen Free Range Grade AA Eggs Over Salmonella Risk

Black Sheep Egg Company is recalling 288,900 dozen Free Range Grade AA Large Brown Eggs sold at retail and wholesale locations in Arkansas and Missouri, with broker distribution in Mississippi, Texas, California and Indiana. The recall cites potential Salmonella contamination as the hazard. Consumers should not consume these eggs and should contact Black Sheep Egg Company for refund or replacement

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

Beckman Coulter Recalls 571 DxI 9000 Immunoassay Analyzers and DxC 500i (2025)

Beckman Coulter recalled 571 DxI 9000 Access Immunoassay Analyzers and DxC 500i Clinical Analyzers distributed worldwide. A software anomaly may prevent correct application of manual dilution factors for tests already in progress on the same Sample ID. Labs should stop using the devices immediately and follow recall instructions.

Beckman Coulter
Beckman Coulter
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Health & Personal Care
HIGH
FDA DEVICE

Kico Knee Innovation ARVIS Shoulder AI Planning Software Recalled for High-Risk Malalignment in 21-0

Kico Knee Innovation recalls 21 ARVIS Shoulder systems nationwide after reports that AI planning software may cause implant malalignment or reduced range of motion. The recall covers software version V2025.1.2 used with IN-27300 hardware. Healthcare providers and patients should stop using the device and follow manufacturer instructions.

Kico Knee Innovation
Complaint identified
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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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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 Recalls Salem Sump Dual-Lumen Stomach Tubes Over ARV Breakage (2025)

Cardinal Health 200 LLC expanded a worldwide recall of Salem Sump silicone dual-lumen stomach tubes after complaints of anti-reflux valve breakage. The valve can fracture under normal use, potentially compromising tube function. Healthcare providers and patients must stop using the device immediately and follow the manufacturer’s recall instructions.

Cardinal Health 200
Firm has
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical ESPOCAN Spinal/Epidural Tray Recalled Over Lid Position Risk

B Braun Medical recalled 10,130 ESPOCAN spinal/epidural trays nationwide after discovering potential for the catheter connector lid to be in an incorrect position. The recall covers multiple product codes and UDI numbers. Healthcare providers must stop using affected units and follow manufacturer instructions for remediation.

B BRAUN MEDICAL
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Cardinal Health 200 Salem Sump Anti-Reflux Valve Recalled for Breakage Risk (2025)

Cardinal Health 200, LLC recalls all lots of the Salem Sump Anti-Reflux Valve worldwide after complaints of valve breakage. The recall covers CE-marked valves with multiple identifiers. Hospitals and clinicians should stop using the device immediately and follow manufacturer instructions. This notice alerts providers to check for the affected code and act now.

Cardinal Health
Firm has
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Tag Statistics

Total Recalls
1,215

Related Tags

poisoning riskimmediate actionstop use immediatelyreturn for refundkitchensummer productfda regulatedcpsc regulatedadult productmandatory standard violationchemical hazardinfant product