kitchen Recalls

378 recalls tagged with “kitchen”.

Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Recalls 8,368 CLEARLINK CONTINU-FLO IV Sets for Leakage Risk (2025)

Baxter Healthcare recalled 8,368 CLEARLINK SYSTEM CONTINU-FLO IV sets nationwide after reports the devices may leak. The non-vented sets include a 0.2-micron filter, three CLEARLINK luer activated valves and a backcheck valve, and measure 102 inches in length. Hospitals and clinicians should stop using these units immediately and follow Baxter's recall instructions.

Baxter Healthcare
IV sets
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Food & Beverages
HIGH
FDA FOOD

Rolling Pin Baking Company Recalls 127,680 Dubai Style Chocolate Pouches for Undeclared Wheat (2025)

Rolling Pin Baking Company LLC is recalling 127,680 Dubai Style Chocolate pouches sold through multiple retailers. The recall was announced on Aug. 29, 2025. The product does not declare wheat in the allergen statement. Consumers should not consume the product and contact the company by email for refund or replacement.

Rolling Pin Baking Company
Product does
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Recalls 136,512 CLEARLINK IV Sets DUO-VENT for Leak Risk (2025)

Baxter Healthcare recalled 136,512 CLEARLINK System Solution Set DUO-VENT IV sets distributed nationwide in the United States after detecting a leak risk. The Luer Activated Valve design may leak, potentially compromising IV administration. Hospitals and patients should stop using the device immediately and follow Baxter recall instructions.

Baxter Healthcare
IV sets
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Food & Beverages
HIGH
FDA FOOD

Herbal Creations Colostrum Powder Recall for Milk Allergen Labeling Error (2025)

Herbal Creations recalls 19,425 kilograms of bulk colostrum powder distributed to 30 US customers after a milk allergen labeling error. The product label does not declare milk as an allergen. Consumers who purchased this product should not consume it and should contact Herbal Creations USA for refund or replacement.

Herbal Creations
Bulk packaged
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Health & Personal Care
HIGH
FDA DEVICE

Northeast Scientific Recalled 561 Units of NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy C

Northeast Scientific recalled 561 units of NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. The recall covers all lots within shelf life ending before August 29, 2026. The hazard is breaches in sterile barrier packaging that could compromise sterility. Stop using the device and follow manufacturer instructions for return or replacement.

Northeast Scientific
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Northeast Scientific NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter Recall 173 Un­

Northeast Scientific recalled 173 units of the NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter distributed nationwide to U.S. healthcare facilities. The device is not cleared for marketing in the United States due to sterility concerns. A breach in the sterile barrier packaging could compromise sterility. Health care providers and patients should stop using the device immediately.

Northeast Scientific
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Northeast Scientific Recalled 1,019 Reprocessed Turbo Elite Atherectomy Catheters Over Sterility Bre

Northeast Scientific Corp. recalled 1,019 units of the NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. The model is not cleared for marketing in the United States. The recall cites potential breaches in sterile barrier packaging that could compromise sterility. Patients and healthcare providers should stop using the device immediately. Follow the manufacturer's recall instructions

Northeast Scientific
Potential for
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Health & Personal Care
HIGH
FDA DRUG

Granules Pharmaceuticals Recalls 3,384 Bottles of Dextroamphetamine ER Capsules for Impurity Issues

Granules Pharmaceuticals Inc. recalls 3,384 bottles of Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate Extended-Release Capsules, 5 mg, 100 capsules per bottle, NDC 70010-029-01, Lot GPC250158A, Exp 06-22-2027. The recall concerns failed impurities/degradation specifications. Healthcare providers and consumers should stop using the

Granules Pharmaceuticals
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DRUG

Ascend Laboratories Recalls ARIPIPRAZOLE 10 mg Tablets Over Superpotent Drug Risks (2025)

Ascend Laboratories, LLC recalls 2,256 bottles of ARIPIPRAZOLE 10 mg tablets distributed nationwide after discovering the product to be superpotent. The recall involves ARIPIPRAZOLE tablets manufactured by Alken Laboratories Ltd. in India and distributed in the United States. The recall date is August 28, 2025, with consumer notification by letter and guidance to stop use.

ARIPIPRAZOLE
Superpotent drug
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Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Skyra MRI System Recall Covers 182 Units Over Ice Blockage Risk

Siemens Medical Solutions USA recalled 182 MAGNETOM Skyra MRI systems worldwide on August 28, 2025. The recall follows a potential ice blockage in the magnet venting system that could cause a helium leak during a quench. Hospitals should stop using affected devices and follow manufacturer instructions for remediation.

Siemens Medical Solutions USA
There is
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Biograph mMR PET-MRI Recall 2025 for Ice Blockage Risk in Venting System (23 Units)

Siemens Medical Solutions USA recalled 23 Biograph mMR PET-MRI systems worldwide after detecting an ice blockage in the magnet venting system. In a magnet quench, helium gas may not escape through vent paths, risking rupture of the helium containment and a leak into the scanning room. Hospitals and providers must stop using the device immediately and follow the manufacturer’s recall instructions.

Siemens
There is
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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Recalls 5 lb Shredded Mozzarella Over Listeria Risk (2025)

Middlefield Original Cheese Cooperative recalled 364.125 cases of 5 lb shredded mozzarella cheese sold to retailers in Ohio, Pennsylvania, Wisconsin and Texas. The product could be contaminated with Listeria monocytogenes. Consumers should not consume it and should contact the cooperative for refund or replacement.

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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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 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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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

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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Tag Statistics

Total Recalls
378

Related Tags

immediate actionstop use immediatelyreturn for refundreplacement availablefda regulatedcpsc regulatedelectronicback to schoolholiday productnhtsa regulatedfederal law violationrepair available