replacement available Recalls

1,215 recalls tagged with “replacement available”.

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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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Pepper Jack Cheese Recalled Over Listeria Risk in 364 Cases

Middlefield Original Cheese Cooperative Pepper Jack Cheese is recalled across Ohio, Pennsylvania, Wisconsin and Texas. The recall covers 364.125 cases, about 7,455 pounds, due to potential contamination with Listeria monocytogenes. Consumers should not consume the product and should contact Middlefield Original Cheese 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

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

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

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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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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Health & Personal Care
HIGH
FDA DRUG

AvKare Chlorpromazine Hydrochloride 50 mg Tablets Recalled for Foreign Substance Contamination (2025

AvKare recalled 1,512 cartons of CHLORPROMAZINE HYDROCHLORIDE 50 mg tablets distributed nationwide in the U.S. for the presence of a foreign substance. The recall is active as of Sept. 17, 2025. Consumers and healthcare providers should stop using this product immediately and contact AvKARE or a healthcare provider for guidance.

AvKare
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Kroger 70% Isopropyl Alcohol Recall Expands for Cross-Contamination Risk

Kroger 70% isopropyl alcohol recall active nationwide, 1860 bottles involved. The recall covers Kroger-branded rubbing alcohol distributed by The Kroger Co. No injuries are reported in the notice. Consumers and healthcare providers should stop using the product immediately and seek guidance from a healthcare professional.

Kroger
Cross Contamination
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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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Health & Personal Care
HIGH
FDA DEVICE

LeMaitre Vascular Artegraft 10-Unit Recall 2025 for Labeling Errors

LeMaitre Vascular recalls 10 Artegraft Collagen Vascular Grafts distributed internationally to Great Britain and Switzerland, with no US distribution. The devices were labeled incorrectly and lacked CE and UKCA marks and missing patient documents. Healthcare providers and patients should stop using the devices and follow recall instructions immediately.

LeMaitre Vascular
Devices were
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Vehicles & Parts
HIGH
NHTSA

Ford Recalls 2025 Explorer and Aviator for Trailer Tail Light Failure (25C42)

Ford recalls 2025 Explorer and Aviator vehicles sold through Ford dealers due to a faulty body control module that can prevent trailer tail lights from illuminating. The defect may reduce visibility for other drivers when towing a trailer. Interim letters alert owners starting Oct 13, 2025, with a final remedy anticipated in April 2026. Ford will perform the repairs at no charge and provide the an

Ford
Trailer tail
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Health & Personal Care
HIGH
FDA DEVICE

CooperVision Recalls 180 Softmed Breathables Toric Lenses Over Invalid Sterilization Cycle (2025)

CooperVision recalled 180 Softmed Breathables toric daily disposable contact lenses after one lot was manufactured with an invalid sterilization cycle. The lenses were distributed across Florida, Kentucky, North Carolina and Wisconsin. Patients should stop using the affected lenses immediately and follow the recall instructions.

CooperVision
One lot
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Vehicles & Parts
HIGH
NHTSA

Ford 2025-2026 F-Series Recalled for Instrument Panel IPC Start-Up Failure (25S88)

Ford is recalling certain 2025-2026 F-550 SD, F-450 SD, F-350 SD, F-250 SD, and 2025 F-150 vehicles because the instrument panel may fail at startup. The recall covers 2025-2026 models. Ford will provide an IPC software update via dealer service or OTA at no cost. Owner letters were mailed September 5, 2025. Contact Ford customer service at 1-866-436-7332. Recall number 25S88.

Ford
An instrument
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Health & Personal Care
HIGH
FDA DEVICE

CooperVision Voyant 1-Day Premium Toric Contact Lens Recalled for Invalid Sterilization Cycle

CooperVision recalled one lot of Voyant 1-Day Premium Toric contact lenses sold nationwide in the United States after an invalid sterilization cycle was detected. The recall affects 90 units distributed in Florida, Kentucky, North Carolina and Wisconsin. Patients should stop using the lenses immediately and contact their eye care professional for guidance.

CooperVision
One lot
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Tag Statistics

Total Recalls
1,215

Related Tags

poisoning riskimmediate actionstop use immediatelyreturn for refundfda regulatedcpsc regulatedkitchengaragelaceration riskchemical hazardelectrical hazardwinter product
    replacement available Recalls | RecallRadar