poisoning risk Recalls

612 recalls tagged with “poisoning risk”.

Food & Beverages
HIGH
FDA FOOD

Willamette Valley Pie Company Recalls 777 Cases of Frozen Bulk Blueberry Crumble Pie ES (2026)

Willamette Valley Pie Company recalled 777 cases of Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case) sold to grocery retailers\' in-store bakeries in Illinois and Oregon after potential contamination with Listeria monocytogenes. The pies are frozen raw and are intended to be baked by the retailer before sale. Retailers and any consumer who may have obtained the product should not use,

Willamette Valley Pie Company
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Made Fresh Salads Scallion Cream Cheese 557 Tub Recall 2026 in New York

Made Fresh Salads Inc. recalled 557 five-pound tubs of Scallion Cream Cheese in New York on February 19, 2026. The recall cites possible contamination with Listeria monocytogenes. Consumers who bought the product should not consume it and should contact Made Fresh Salads for refunds or replacements.

Made Fresh Salads
Products may
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Food & Beverages
HIGH
FDA FOOD

Made Fresh Salads Vegetable Cream Cheese Recall 557 5-lb Tubs (2026)

Made Fresh Salads recalled 557 tubs of Vegetable Cream Cheese sold in New York after a potential Listeria monocytogenes contamination. The recall covers all expiration dates through 02/27/2026. Consumers who bought this product should not eat it and should contact Made Fresh Salads Inc for refund or replacement by telephone.

Made Fresh Salads
Products may
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Food & Beverages
HIGH
FDA FOOD

Made Fresh Salads Recalls 557 Walnut Raisin Cream Cheese 5 lb Tubs Over Listeria Risk (2026)

Made Fresh Salads recalled 557 five‑pound tubs of Walnut Raisin Cream Cheese distributed in New York after identifying a potential Listeria monocytogenes contamination. The product is a Walnut Raisin Cream Cheese in a 5‑pound white plastic tub. Consumers who bought this product should not consume it and should contact Made Fresh Salads Inc for refunds or replacements by telephone.

Made Fresh Salads
Products may
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Food & Beverages
HIGH
FDA FOOD

Made Fresh Salads Apple Cinnamon Cream Cheese 5-Lb Tub Recalled for Listeria Contamination (2026)

Made Fresh Salads recalled 557 five-pound Apple Cinnamon Cream Cheese tubs distributed in New York after an FDA enforcement report due to Listeria monocytogenes contamination. The contamination poses a risk of serious illness if consumed. Consumers should not eat the product and should contact Made Fresh Salads Inc for refunds or replacements by telephone.

Made Fresh Salads
Products may
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Food & Beverages
HIGH
FDA FOOD

557 Made Fresh Salads Lox Cream Cheese Tubs Recalled for Listeria Risk

Made Fresh Salads recalled 557 five-pound tubs of Lox Cream Cheese due to possible Listeria monocytogenes contamination. This contamination poses serious health risks, especially to vulnerable groups. Consumers should not eat this product and should contact Made Fresh Salads for a refund.

Made Fresh Salads
Products may
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Food & Beverages
HIGH
FDA FOOD

Made Fresh Salads Garlic & Herb Cream Cheese 5 lb Tub Recalled for Listeria Contamination (2026)

Made Fresh Salads Inc recalled 557 five-pound tubs of Garlic & Herb Cream Cheese sold in New York after a confirmed Listeria monocytogenes contamination. The recall was activated on February 19, 2026 and remains active as of March 18, 2026. Consumers who purchased the product should not consume it and should contact the company for refund or replacement guidance.

Made Fresh Salads
Products may
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Recalled Joly's 80% Vinegar (32 oz, pack of two) Product packaging
HIGH
CPSC

Joly's Recalls 80% Vinegar Due to Poisoning and Burn Risks

Joly's LLC recalled 80% Vinegar on February 19, 2026, due to serious risks of poisoning and chemical burns. The product lacks essential warning labels and first aid instructions, violating federal safety laws. Consumers should stop using the product immediately and seek a refund.

Joly's LLC, of Orlando, Florida
The recalled
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Health & Personal Care
HIGH
FDA DRUG

Kirkman MAXIMUM Zone 1 4% Lidocaine Cream Recall 178 Bottles (2026)

Kirkman recalled 178 bottles of MAXIMUM Zone 1 4% Lidocaine Cream distributed nationwide in the U.S. by Dermal Source. The recall cites stability data that does not support the stated expiry date. Consumers and healthcare providers should stop using this product immediately and contact Kirkman for guidance.

Kirkman
Stability Data
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Health & Personal Care
HIGH
FDA DEVICE

Medline Airway Exam Kit Recalled for 14,379 Units Over Olympus Valve Detachment (2026)

Medline Industries, LP recalled 14,379 Airway Exam Kits containing Olympus biopsy valves nationwide. The recall cites rubber fragments detaching from the slit of single-use biopsy valves. Potential harm includes a foreign body in the patient’s tracheobronchial tree, inflammatory response, hypoxia, and longer procedures. Providers and patients should stop using the kit and follow recall directions.

Medline Industries, LP
Kits contain
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed Paradigm Real-Time Insulin Pump Recalled for 29,074 Units Worldwide (2026)

Medtronic MiniMed recalled 29,074 Paradigm Real-Time insulin pumps worldwide. The devices may deliver insulin improperly when the pump is elevated or lowered relative to the infusion site due to gravitational effects. Patients should stop using the pumps immediately and follow recall instructions from the manufacturer and their healthcare provider.

Medtronic MiniMed
All Medtronic
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Health & Personal Care
HIGH
FDA DRUG

Harbin Jixianglong Biotech Semaglutide Rx Compounding Recall (2026)

Harbin Jixianglong Biotech Co. recalled semaglutide for Rx compounding use distributed nationwide to healthcare providers in the United States. The recall cites CGMP deviations and failure to complete process validation and bacterial endotoxin method validation before distribution. Healthcare providers and patients should stop using this product immediately and contact the manufacturer or their CL

Harbin Jixianglong Biotech Co.
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Harbin Jixianglong Biotech Semaglutide Rx Compounding Recall 2026 — 6 Packaging Sizes

Harbin Jixianglong Biotech Co. recalled Semaglutide for Rx compounding use nationwide in the United States. The recall cites CGMP deviations and failure to complete endotoxin validation before distribution. Healthcare providers and patients should stop using the product immediately and contact the company or a healthcare provider for guidance via email.

Harbin Jixianglong Biotech Co.
CGMP Deviations
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Food & Beverages
HIGH
FDA FOOD

Oregon Potato Company Recalls Blueberries Due to Listeria Risk

Oregon Potato Company recalled 55,689 pounds of IQF Blueberries on February 12, 2026, due to potential contamination with Listeria monocytogenes. The affected products include 30-pound cases and 1,400-pound totes distributed in Michigan, Oregon, Washington, Wisconsin, and Canada.

Oregon Potato Company
Listeria monocytogenes
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Blockers Recalled for Attenuation Degradation in 51 Units Worldwide (2026)

Burlington Medical recalled 51 Blocker devices sold worldwide after a recall notice. The devices may degrade attenuation over time, shortening their lifespan. Stop using the devices immediately and follow the manufacturer’s recall instructions. Contact Burlington Medical, LLC or your healthcare provider for guidance. Distribution is worldwide.

Burlington Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Embrace Drill Tower Recall 74 Units in 2026

Waldemar Link GmbH & Co. KG recalls 74 Embrace Drill Tower devices distributed in 15 U.S. states. The recall notes mixed-up article numbers in the overview of the instruments. The surgical steps are correct. Stop using the device immediately and follow manufacturer instructions.

Waldemar Link GmbH & Co. KG
The surgical
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Food & Beverages
CRITICAL
FDA FOOD

Juniper Granola Junebar Peanut Chocolate Chip Snack Bar Recalled in 2026

Juniper Granola recalled 1,800 Junebar Peanut Chocolate Chip All Natural Snack Bars sold in New York after undeclared milk and soy were found. The product can cause severe allergic reactions in milk or soy allergic individuals. Stop using the bars and contact Juniper Granola for a refund or replacement.

Juniper Granola
Products contain
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Food & Beverages
HIGH
FDA FOOD

Juniper Granola Junebar Recall 2026: 1,800 Snack Bars Recalled for Undeclared Milk and Soy

Juniper Granola recalled 1,800 Junebar Chocolate Cherry All Natural Snack Bars sold in New York after undeclared milk and soy were found. The bars carry Lot L1300 and variants L1300A and L1300B. They were produced in a facility that also processes gluten, peanuts, and sesame. Consumers should not eat these bars and should contact Juniper Granola for refunds or replacements.

Juniper Granola
Products contain
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Tag Statistics

Total Recalls
612

Related Tags

kitchenfda regulatedimmediate actionstop use immediatelyreturn for refundreplacement availablecpsc regulatedplasticlithium batteryelectronicnhtsa regulatedfederal law violation