garage Recalls

100 recalls tagged with “garage”.

Health & Personal Care
HIGH
FDA DEVICE

Applied Medical Technology NutraGlide ENFit Nasal Feeding Tube Recall 840 Units (2025)

Applied Medical Technology recalled 840 NutraGlide ENFit nasal feeding tubes distributed in the United States to Massachusetts and Rhode Island. The tubes have distal tips that may detach at lower than expected forces. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.

Applied Medical Technology
The nasal
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Health & Personal Care
HIGH
FDA DEVICE

AVID Medical CPT BASIC IR PACK 1646381 Recall for Sterility Risk (2025)

AVID Medical recalls 228 CPT BASIC IR PACKs sold nationwide, including Florida, due to open header bag seals that may compromise sterility. The recall is active as of September 17, 2025. Consumers should stop use and follow manufacturer instructions.

AVID Medical
Potential for
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Recalled Cosco 2-Step Kitchen Stepper model 11349WHG1E
MEDIUM
CPSC

Cosco 2-Step Kitchen Stepper Recall 2025 — 10 Models Affected

Dorel Home Furnishings recalls Cosco 2-Step Kitchen Steppers sold at multiple retailers after reports that the safety bar can detach or break during use. The recall covers 10 model numbers. Consumers should stop using the safety bar immediately and contact Dorel for a free repair kit.

Dorel Home Furnishings
The safety
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Recalled RIDGID 18Volt Brushless 21-Degree Framing Nailer
MEDIUM
CPSC

RIDGID 18V Framing Nailers Recalled for Laceration Hazard (2025)

RIDGID 18V Brushless framing nailers, sold through multiple retailers nationwide, are recalled. The recall covers two models with serial-number ranges CS21146D220001 to CS24165N220001 and CS21275D220001 to CS24165N220001. The dual action engagement system can discharge a nail with the trigger alone, creating a laceration hazard.

RIDGID
The dual
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Vehicles & Parts
HIGH
NHTSA

Ford 2025 Expedition Recalled for Brake Software Issue; OTA Update Available

Ford Motor Company recalls 2025 Expedition and other models over a brake booster software fault. The Electronic Brake Booster module may fail while driving or during ADAS use, reducing power brake assist. Ford will update the module software OTA or via dealer free of charge. Owner notifications started August 22, 2025. Contact Ford at 1-866-436-7332 for details and recall 25S77.

Ford
An unexpected
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Health & Personal Care
HIGH
FDA DEVICE

Home Health US Recalled 4,661 One Step Sterile Lancets for Single Use (2025)

Home Health US recalled 4,661 One Step Sterile Lancets for Single Use sold nationwide through Amazon. The recall cites incorrect or missing Unique Device Identifier codes. Consumers should stop using the lancets immediately and follow the recall instructions from Home Health US or their healthcare provider.

Home Health US
Due to
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Vehicles & Parts
HIGH
NHTSA

Hyundai IONIQ 5 2025 Recall for High Voltage Battery Bus Bar Tightening Short Circuits (2025)

Hyundai Motor America recalls 2025 IONIQ 5 vehicles due to a potentially loose bus bar in the high voltage battery system. The recall covers 2025 IONIQ 5 models. Hyundai says a short circuit could cause a fire. Owners should park outside away from structures until the remedy is complete and contact Hyundai at 1-855-371-9460. The recall number is 280.

Hyundai
An electrical
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Recalled HydroTech 5/8-inch x 25-foot Expandable Burst-Proof Hose
MEDIUM
CPSC

Winston Products HydroTech 5/8-Inch Expandable Burst-Proof Hose Recall 2025

Winston Products recalled HydroTech 5/8-inch Expandable Burst-Proof Hoses sold through Home Depot and Walmart. The hoses manufactured on or before August 31, 2024 can burst and create an impact hazard and temporarily impair hearing. Consumers should stop using the hoses immediately and contact Winston Products for a full refund.

Winston Products
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

DJO Surgical Recalls 447 ALTIVATE Reverse Glenoid Reamer Sleeve Units (2025)

DJO Surgical is recalling 447 ALTIVATE Reverse Glenoid Reamer Sleeve devices distributed nationwide in the United States. The device may kick or bind up during or immediately prior to use. Healthcare providers and patients should stop using the device and follow recall instructions issued by Encore Medical, LP via email.

DJO Surgical
Their is
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Recalled WLIVE Fabric 15-Drawer Dresser in Rustic Brown
HIGH
CPSC

WLIVE Fabric 15-Drawer Dressers Recalled for Tip-Over Risk Sold on Amazon (2025)

WLIVE recalled its Fabric 15-Drawer Dressers sold on Amazon after reports of tip-over and entrapment hazards. The dressers can tip when not anchored to a wall, posing serious injury or death risk to children and violating the STURDY standard. Consumers should stop using unanchored dressers and contact WLIVE for a full refund.

WLIVE
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Mobile X-ray System Recall for 1 Unit Over Water Exposure Cleaning Hazard (2025)

Sedecal SA recalls 1 unit of Model 40KWMOBILE3.899 Mobile X-ray system distributed to consignees in the United States, including California, Illinois and New Jersey. The device is not water-resistant and must be cleaned strictly according to the manual, with the notice outlining the potential consequences of improper cleaning. Healthcare providers and patients should stop using the device immediat

Sedecal
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA SM-40HF-B-D-C Mobile X-ray System Recall for Cleaning Not Water-Resistant Risk (2025)

Sedecal SA recalled 1 mobile X-ray system in the United States. The device is distributed in CA, IL and NJ. The system is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could have unspecified consequences. Clinicians and facilities should stop using the device and follow manufacturer instructions.

Sedecal
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls 1 Unit 40KW-FX.899 Mobile X-ray System Over Cleaning Hazard (2025)

Sedecal SA recalled 1 unit of the 40KW-FX.899 Mobile X-ray System distributed to CA, IL and NJ. The device is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could cause adverse effects. Stop using the device and contact Sedecal SA or a healthcare provider for instructions.

Sedecal SA
Sedecal sent
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Food & Beverages
HIGH
FDA FOOD

PRIMO NO. 1 IN PRODUCE Recalled 89 Boxes of Sliced Cucumber for Salmonella Contamination (2025)

PRIMO NO. 1 IN PRODUCE recalled 89 boxes of sliced cucumber packaged in 2/10-lb boxes distributed to Virginia, New York, Pennsylvania and New Jersey after Salmonella contamination. The recall is active and classified as high risk. Consumers should not eat the product and should contact PRIMO NO. 1 IN PRODUCE for refund or replacement.

PRIMO NO. 1 IN PRODUCE
Product contaminated
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Food & Beverages
HIGH
FDA FOOD

Chefs Warehouse Recalls 5 lb Diced Cucumber for Salmonella Contamination (2025)

Chefs Warehouse recalled 5 lb diced cucumber distributed to Maryland, Delaware and Virginia after FDA confirmation of Salmonella contamination. The product is a 5 lb bag labeled 5# Lot#B0515911. Consumers should not consume the recalled cucumber and should contact Chefs Warehouse for refund or replacement.

Chefs Warehouse
Product is
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Vehicles & Parts
HIGH
NHTSA

Honda ADV160 Recall 2025 for Oil Pump Gear Loss of Drive Power

Honda recalled 2024-2025 ADV160 scooters after discovering the oil pump driven gear may fail, causing a loss of drive power. The loss of drive power could lead to a crash. Owner letters were mailed August 6, 2025, and dealers will replace the gear free of charge under recall KR9.

Honda
Loss of
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