stop use immediately Recalls

2,153 recalls tagged with “stop use immediately”.

Health & Personal Care
HIGH
FDA DEVICE

Tandem Diabetes Care Recalling 19 Units of t:slim X2 Insulin Pump Over RTL App Defect (2025)

Tandem Diabetes Care recalls 19 units of the t:slim X2 insulin pump with interoperable technology distributed internationally, including Israel. An app defect occurs when the phone uses a right-to-left language and can cause app-pump pairing problems and graphical defects. Patients should stop using the device immediately and follow the manufacturer’s recall instructions.

Tandem Diabetes Care
an app
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Food & Beverages
HIGH
FDA FOOD

Evergreen Orchard Farm Korean Pear Juice Recalled for 610 Cases in 2025

Evergreen Orchard Farm recalled 610 cases of Korean Pear Juice distributed in Pennsylvania, New Jersey and New York after finding a lack of pasteurization and sanitation records. The recall highlights a potential adulteration risk. Consumers who purchased this product should not drink it and should contact Evergreen Orchard Farm for refunds or replacements via email.

Evergreen Orchard Farm
Lack of
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Food & Beverages
HIGH
FDA FOOD

Evergreen Orchard Farm Grape Juice Recalled in 78 Cases for 2025 Pasteurization Lapse

Evergreen Orchard Farm recalled 78 cases of Grape Juice in 4 oz foil pouches distributed to PA, NJ and NY. The recall cites lack of pasteurization and sanitation records. Consumers who purchased the product should not consume it and should contact Evergreen Orchard Farm, LLC via Email for refund or replacement.

Evergreen Orchard Farm
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

North American Rescue JETT Medical Device Recall for Lower-Limb Occlusion Tool (2025)

North American Rescue recalled 552 units of the JETT device, used for occlusion of blood flow to the lower limbs, due to a manufacturing defect that may compromise structural integrity and performance. The recall covers multiple kits distributed worldwide, including U.S. states and several international countries. Stop using the device immediately and await recall instructions from the company or

North American Rescue
Device used
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Vehicles & Parts
HIGH
NHTSA

Honda 2025 CR-V Hybrid Recall for Fuel Hose Installation Could Cause Fire (TLS)

Honda recalls 2025 CR-V Hybrid vehicles sold through Honda dealers nationwide after finding an improperly installed fuel feed hose that may leak. The recall is identified by Honda as TLS. Dealers will replace the fuel feed hose and install a new connector cover at no charge. Owners should contact Honda at 1-888-234-2138 for service.

Honda
A fuel
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Vehicles & Parts
HIGH
NHTSA

VOLKSWAGEN Atlas Recall 2025 for Service Brakes Bolts in Atlas, Atlas Cross Sport, ID.4

Volkswagen Group of America recalls 2023-2025 Atlas, Atlas Cross Sport and 2023-2024 ID.4 models for loose bolts in the chassis, brake system and suspension. The potential consequence is loss of vehicle control and a crash risk. Owners should stop driving the vehicle and contact a dealer for inspection; recall letters were mailed on July 25, 2025.

Volkswagen
A loss
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Deep Sprouted Mat 16 oz Recalled for Salmonella Risk 2025

CHETAK NEW YORK LLC recalled 5,232 packets of Deep Sprouted Mat 16 oz distributed to California, New Jersey, Illinois, Florida and Texas after tests found Salmonella. The recall class is I with a high hazard level. Consumers should not consume the product and should seek refund or replacement by email.

CHETAK NEW YORK
Product tested
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Vehicles & Parts
HIGH
NHTSA

Ford recalls 2025 Expedition air bags for passenger-side deployment risk

Ford Motor Company recalls certain 2025 Expedition and Navigator vehicles due to a passenger-side frontal air bag that may deploy with excessive force. Dealers will replace the passenger side air bags at no charge. Owner notification letters were mailed August 8, 2025.

Ford Motor Company
An air
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Health & Personal Care
HIGH
FDA DEVICE

bioMerieux VITEK 2 AST Cards Recalled for False Colistin Results (235,269 Cards) 2025

bioMerieux recalled 235,269 VITEK 2 Gram-negative AST test cards containing Colistin cs02n, distributed internationally. The cards may produce false resistant results for Colistin when testing certain multi-drug-resistant bacteria. Healthcare providers should stop using the affected cards immediately and follow the recall instructions from bioMerieux.

bioMerieux
Potential for
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Food & Beverages
HIGH
FDA FOOD

BulkSupplements.com Inositol Recall Affects 1,001 Units Over Possible Staphylococcus Contamination (

BulkSupplements.com recalled 1,001 units of Inositol powder sold in the U.S. and abroad after potential contamination with Staphylococcus aureus. The finished product was distributed by Hard Eight Nutrition LLC dba BulkSupplements.com and classified as a Class II recall. Consumers should stop using the product and seek refunds or replacements from the company.

BulkSupplements.com
Finished product
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Vehicles & Parts
HIGH
NHTSA

GM Recalls 2024-2025 Chevrolet Blazer EV for Parking Brake Wiring Harness Issue

GM recalls 2024-2025 Chevrolet Blazer EVs due to a rear parking brake wiring harness that may corrode or become damaged. The defect can cause unintended parking brake activation or loss of function, increasing crash risk. Dealers will inspect and reroute the harness, install anti-abrasive tape, and replace damaged harnesses at no cost. Owner notices mailed October 1, 2025. Contact Chevrolet at 1-[

CHEVROLET
Unintended activation
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Health & Personal Care
HIGH
FDA DEVICE

Orthofix Pillar SA Ti Spinal Implant Recalled for Labeling Error (2025)

Orthofix U.S. recalled 3 Pillar SA Ti intervertebral body fusion devices nationwide in the United States after a labeling discrepancy. The 37 mm implant width is correct on the front label, but the outer side flap and inner label information box incorrectly state 33 mm. Healthcare providers and patients should stop using the device immediately and await manufacturer instructions.

Orthofix U.S.
A 37
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Food & Beverages
HIGH
FDA FOOD

Nirwana Foods Golden Raisin Recalled for Undeclared Sulfites in 28 oz Bags (2025)

Nirwana Foods recalled Golden Raisin sold in New Jersey and New York after undeclared sulfites were detected. The packaging did not declare sulfites. Consumers should not consume the product and should contact Nirwana Foods LLC for refund or replacement information using one of several notification methods.

Nirwana Foods
Undeclared Sulfites
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Food & Beverages
HIGH
FDA FOOD

Vitalabs Vitamin B12 Raspberry Gummies Recall for Peanut Allergen (2025) — 9,657 Bottles

Vitalabs recalled 9,657 bottles of Vitamin B12 Raspberry Gummies sold under Black Girl Vitamins and Rise-N-Shine brands after suppliers flagged undeclared peanuts. The product may contain peanuts not disclosed on the label, creating a peanut allergy risk. Consumers should stop using the product and contact Vitalabs for refund or replacement.

Vitalabs
Undeclared Peanuts.
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalled 5 SM-40HF-B-D-C Mobile X-ray Systems Over Cleaning Risk (2025)

Sedecal SA recalled 5 SM-40HF-B-D-C Mobile X-ray systems distributed in California, Illinois and New Jersey after notifying consignees via email. The notice says the equipment is not water-resistant and must be cleaned strictly per the manual. Hospitals and clinics should stop using the devices immediately and follow the recall instructions.

SEDECAL SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalled 5 SM-40HF-B-D-C Mobile X-ray Systems for Cleaning Warning (2025)

Sedecal SA recalled 5 SM-40HF-B-D-C 40KW 55G Mobile X-ray systems distributed in the US (CA, IL, NJ) after warning that the equipment is not water-resistant and must be cleaned strictly per the manual. The notice outlines the possible consequences of improper cleaning. Healthcare facilities should stop using the devices immediately and contact Sedecal SA for instructions.

Sedecal SA
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Easy Moving Plus Mobile X-ray System Recalled for Cleaning Not Water-Resistant Risk (8 Units

Sedecal recalled 8 units of the Easy Moving Plus mobile X-ray system distributed in California, Illinois and New Jersey. The devices are not water-resistant and cleaning must follow the manual to avoid the consequences of improper cleaning. Stop using the device and contact Sedecal SA or your healthcare provider for instructions.

Sedecal
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Recalled 7 Mobile X-ray Systems Over Cleaning Not Water-Resistant Issue (2025)

Sedecal recalled 7 mobile X-ray systems distributed to California, Illinois and New Jersey after warning that the equipment is not water-resistant and must be cleaned strictly per the manual. The notice highlights potential consequences of improper cleaning. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.

Sedecal SA
Sedecal sent
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Tag Statistics

Total Recalls
2,153

Related Tags

immediate actionelectronicelectrical hazardpet relatedinfant producttip over riskreplacement availablefda regulatedcpsc regulatednhtsa regulatedpoisoning riskreturn for refund