explosion risk Recalls

77 recalls tagged with “explosion risk”.

Health & Personal Care
HIGH
FDA DEVICE

Philips Respironics Trilogy EV300 Ventilator Recall Affects 113,717 Units in 2026

Philips Respironics recalled 113,717 Trilogy EV300 ventilators sold in the United States and internationally after determining the Obstruction Alarm may fail to trigger within required standards. The alarm can delay alerting caregivers for up to four breaths. Patients and healthcare providers should stop using the device immediately and follow recall instructions from Philips or their clinician.

Philips Respironics
In some
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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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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 DRUG

Kirkman MAXIMUM ZONE 2 4% Lidocaine Cream Recall for Expiry Stability Issue (2026)

HTO Nevada Inc. dba Kirkman recalled 243 bottles of MAXIMUM ZONE 2, 4% lidocaine cream distributed nationwide by Dermal Source. The recall cites stability data that does not support an expiry date. Consumers and healthcare providers should stop using this product immediately and contact Kirkman for guidance.

HTO Nevada Inc. dba 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 720G Insulin Pump Recall 2026 Affects 37,458 Units Worldwide

Medtronic MiniMed recalled 37,458 insulin pumps sold worldwide through healthcare providers, including the MiniMed 720G, after finding that a pump raised above or lowered relative to the infusion site can deliver insulin too much or too little. The defect stems from changes in gravitational force affecting hydrostatic and hydrodynamic pressures at the infusion site. Patients should stop using the

Medtronic MiniMed
All Medtronic
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Health & Personal Care
HIGH
FDA DEVICE

Ion Beam Applications PROTEUS 235 Recalled for 4 Units Worldwide (2026)

Ion Beam Applications S.A. recalled four PROTEUS 235 proton therapy systems distributed worldwide, including Florida in the United States, and the countries of Italy and Japan. The defect disables the Therapy Safety System's Universal Beam Triggering Interface, so the system may not stop beam delivery if the Healthy Signal from an external gating device is lost. Patients and healthcare providers应该

Ion Beam Applications
It was
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Food & Beverages
HIGH
FDA FOOD

Mangalm Tops GOLD Mixed Pickle Recalled for Erucic Acid Adulteration Risk (2026)

Mangalm LLC recalled Tops GOLD Mixed Pickle sold in California, Nevada, Oregon, Utah and Washington after FDA enforcement. The product may be adulterated with erucic acid from mustard oil. Consumers who purchased it should not eat it and should contact Mangalm for refund or replacement via email.

Mangalm
Potential adulteration
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Health & Personal Care
HIGH
FDA DRUG

Dynarex BZK Antiseptic Towelettes 100-Count Recalled for CGMP Deviations (2026)

Dynarex recalled 100-pack BZK Antiseptic Towelettes sold nationwide after FDA enforcement cited CGMP deviations. The recall covers multiple lots, including Lot 52347-R, 52348-R, 52349-R, 52350, 52351-R, 52352, Exp. Date Mar 2027 and Exp. Date Jun 2027. Consumers should stop using the product immediately and contact ACME UNITED CORPORATION or their healthcare provider for guidance.

Dynarex
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Dukal BZK Antiseptic Towelettes Recalled for CGMP Deviations (2026)

Nationwide recall of Dukal BZK Antiseptic Towelettes due to CGMP deviations. The products are manufactured for Dukal, LLC in Ronkonkoma, NY and distributed across the United States. Stop using immediately and contact ACME United Corporation for guidance.

Dukal
CGMP Deviations
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Health & Personal Care
HIGH
FDA DEVICE

Medline Dialysis Kits Recalled Over Silicone Seal Issues

Medline Industries recalled 14,525 dialysis convenience kits on January 8, 2026. The recall affects multiple product SKUs due to potential silicone seal failures. These issues may cause therapy delays or exposure to contaminants.

Medline Industries, LP
Affected lots
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Health & Personal Care
HIGH
FDA DRUG

Tylenol Recall by Gold Star Distribution Affects 5 SKUs in 2026

Gold Star Distribution is recalling Tylenol products distributed nationwide. The recall concerns CGMP deviations and insanitary conditions at the distributor’s facility. Consumers should stop using these Tylenol products immediately and contact Gold Star Distribution for guidance.

Gold Star Distribution
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

GOLD STAR DISTRIBUTION Vaporizing Chest Rub Recall 2026 All Lots Nationwide

Gold Star Distribution is recalling all lots of its Vaporizing Chest Rub, 4 oz, 12-count, UPC 048155903319, distributed nationwide in the United States. The recall, number D-0283-2026, stems from CGMP deviations including insanitary conditions with rodent exposure/activity at the distribution center. Consumers and healthcare providers should stop using the product immediately and contact Gold Star

Gold Star Distribution
CGMP Deviations:
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Recalled Uuoeebb Infant Walker in gray
HIGH
CPSC

BaoD Recalls Uuoeebb Infant Walkers Sold on Amazon for Fall and Entrapment Hazards (2025)

BaoD recalled Uuoeebb Infant Walkers sold on Amazon after safety hazards were identified. The walker can fit through a standard doorway and does not stop at a step edge, creating a fall hazard. The leg openings can allow a child to slip down until the head becomes entrapped. Consumers should stop using the recalled walker immediately and contact BaoD for a full refund.

Uuoeebb
The recalled
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Vehicles & Parts
HIGH
NHTSA

Jeep Wagoneer and Grand Wagoneer Exterior Trim Recall 2025 for Detachment Hazard

Chrysler's Jeep Wagoneer and Grand Wagoneer SUVs are recalled in 2025 for exterior door trim that may detach. The recall is issued through FCA US dealer networks. Dealers will inspect and replace trim free of charge. Owner letters were mailed Sept. 25, 2025. VINs are searchable on NHTSA.gov beginning Sept. 18, 2025.

Chrysler
Detached trim
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Vehicles & Parts
HIGH
NHTSA

Ford recalls 2025 Explorer and other models for possible fuel injector leak linked to fire risk (24S

Ford Motor Company recalled 2023 Lincoln Corsair, 2023-2024 Escape, 2024 Mustang, and 2025 Explorer vehicles due to fuel injector assembly lacking O-ring support discs. The defect may cause a fuel leak with ignition risk. Dealers will install new fuel injector O-rings and O-ring support discs at no charge. Owner letters mailed Oct 7, 2024. Ford contact: 1-866-436-7332. Recall number 24S54.

Ford Motor Company
A fuel
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Blood Type Test Recalled for Lack of Premarket Approval (47 Units) 2025

GET TESTED INTERNATIONAL AB recalled 47 Blood Type Test units distributed nationwide in the United States after discovering the device was distributed without FDA premarket approval or clearance. The hazard is distribution without FDA premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and contact GET TESTED INTERNATIONAL AB for instructions.

GET TESTED INTERNATIONAL AB
Distribution without
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Tag Statistics

Total Recalls
77

Related Tags

immediate actionreturn for refundfda regulatedcpsc regulatedelectrical hazardholiday productinfant productadult productstop use immediatelyreplacement availablebedroomliving room