Estados Unidos Recalls

Retiros de seguridad del consumidor de la FDA, CPSC, NHTSA y USDA FSIS.

Showing 24 of 17,562 results
Safety AlertUSRSS Feed

Kettle Cuisine Recalls Marketside Tomato Bisque Soup Kit – Sold Exclusively at Walmart Stores Because of Possible Health Risk

Unknown Firm
RSS FeedGeneral Alert

Kettle Cuisine Recalls Marketside Tomato Bisque Soup Kit – Sold Exclusively at Walmart Stores Because of Possible Health Risk

Aug 12, 2026
Food & BeverageUSFDA Food

Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intended Use: take 2 capsules per day. Route of Administration: OraI. Manufactured for Zen Principle 774 Mays Blvd Incline Village, NV 89451. The product is offered as a 1-pack (180 capsules; Amazon code/FNSKU X000ZJJ4FT) and as a 2-pack (twin pack, 360 capsules; Amazon code/FNSKU X00159YJXP).

FACTORY6, INC.
FDA FoodClass I

Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intended Use: take 2 capsules per day. Route of Administration: OraI. Manufactured for Zen Principle 774 Mays Blvd Incline Village, NV 89451. The product is offered as a 1-pack (180 capsules; Amazon code/FNSKU X000ZJJ4FT) and as a 2-pack (twin pack, 360 capsules; Amazon code/FNSKU X00159YJXP).

Possible Salmonella in Moringa Leaf Powder product.

Aug 12, 2026FACTORY6, INC.
Medical DeviceUSFDA Devices

HardyDisk AST Cefiderocol 30¿g (FDC30) REF Z9435 HardyDisk AST Cefiderocol 30¿g (FDC30) for in vitro agar diffusion susceptibility testing is indicated when there is the need to determine the susceptibility of Enterobacterales, Pseudomonas aeruginosa, Acinetobacter baumannii complex and Stenotrophomonas maltophilia to Cefiderocol,

Hardy Diagnostics
FDA DevicesClass II

HardyDisk AST Cefiderocol 30¿g (FDC30) REF Z9435 HardyDisk AST Cefiderocol 30¿g (FDC30) for in vitro agar diffusion susceptibility testing is indicated when there is the need to determine the susceptibility of Enterobacterales, Pseudomonas aeruginosa, Acinetobacter baumannii complex and Stenotrophomonas maltophilia to Cefiderocol,

Due to incorrect cartridges include in affected products that there is the potential for false-susceptible or false-resistant susceptibility results and may lead to selection of an ineffective antimicrobial therapy, potentially resulting in delayed appropriate treatment, prolonged infection, or worsening clinical outcome.

Aug 12, 2026Hardy Diagnostics
Food & BeverageUSFDA Food

Clover Hill Dairy LLP, sharp cheese variety (Cheddar, Yummy Cheddar, White Cheddar, Monterey Jack). Sold in approximate 1/2-lb, 1-lb, 2.5-lb, and 5-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.

Clover Hill Dairy, LLC
FDA FoodClass I

Clover Hill Dairy LLP, sharp cheese variety (Cheddar, Yummy Cheddar, White Cheddar, Monterey Jack). Sold in approximate 1/2-lb, 1-lb, 2.5-lb, and 5-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.

Product contaminated with Listeria monocytogenes.

Aug 12, 2026Clover Hill Dairy, LLC
PharmaceuticalUSFDA Drugs

Dicyclomine Hydrochloride Capsules, USP, 10mg, 1,000 bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India, NDC 59651-719-99

Aurobindo Pharma USA Inc
FDA DrugsClass II

Dicyclomine Hydrochloride Capsules, USP, 10mg, 1,000 bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India, NDC 59651-719-99

shortfill; reports of empty capsules.

Aug 12, 2026Aurobindo Pharma USA Inc
Medical DeviceUSFDA Devices

Brand Name: Quantum Rehab Product Name: Quantum Rival Model/Catalog Number: Quantum Rival Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller

Pride Mobility Products Corp.
FDA DevicesClass II

Brand Name: Quantum Rehab Product Name: Quantum Rival Model/Catalog Number: Quantum Rival Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller

If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

Aug 12, 2026Pride Mobility Products Corp.
Medical DeviceUSFDA Devices

Brand Name: Quantum Rehab Product Name: Q6 Edge HD Model/Catalog Number: Q6 Edge HD Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller

Pride Mobility Products Corp.
FDA DevicesClass II

Brand Name: Quantum Rehab Product Name: Q6 Edge HD Model/Catalog Number: Q6 Edge HD Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller

If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

Aug 12, 2026Pride Mobility Products Corp.
Medical DeviceUSFDA Devices

Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number: NCOCO2075 Software Version: N/A Product Description: In situ polymerizing peripheral nerve repair device Component: No

TISSIUM SA
FDA DevicesClass II

Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number: NCOCO2075 Software Version: N/A Product Description: In situ polymerizing peripheral nerve repair device Component: No

Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device beyond its validated shelf life may result in perioperative breakage of the device rendering device unusable; worst-case outcome would be revision surgery.

Aug 12, 2026TISSIUM SA
Vehicle RecallUSNHTSA

Mack Trucks, Inc. - Marker Lights May Fail to Illuminate/FMVSS 108

Mack Trucks, Inc.
NHTSAGeneral Alert

Mack Trucks, Inc. - Marker Lights May Fail to Illuminate/FMVSS 108

Marker lights that fail to illuminate can reduce visibility, increasing the risk of a crash.

Aug 12, 2026Mack Trucks, Inc.
Medical DeviceUSFDA Devices

FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 UDI-DI code: (01)00851458005136 The FilmArray NGDS Warrior Panel is a qualitative, multiplexed, nucleic acid-based in vitro diagnostic test intended for use with the FilmArray 2.0 system. The FilmArray NGDS Warrior Panel detects and identifies Bacillus anthracis, Yersinia pestis, Francisella tularensis, Coxiella burnetii, Ebola virus, and Marburg virus nucleic acids directly from human whole blood (EDTA).

Biofire Defense
FDA DevicesClass II

FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 UDI-DI code: (01)00851458005136 The FilmArray NGDS Warrior Panel is a qualitative, multiplexed, nucleic acid-based in vitro diagnostic test intended for use with the FilmArray 2.0 system. The FilmArray NGDS Warrior Panel detects and identifies Bacillus anthracis, Yersinia pestis, Francisella tularensis, Coxiella burnetii, Ebola virus, and Marburg virus nucleic acids directly from human whole blood (EDTA).

Firm has identified mismatches between the outbreak strain and the reference strain used in the development of its qualitative, multiplexed, nucleic acid-based in vitro diagnostic panel test.

Aug 12, 2026Biofire Defense
Medical DeviceUSFDA Devices

Merge PACS, medical imaging diagnostic workstation

Merge Healthcare, Inc.
FDA DevicesClass II

Merge PACS, medical imaging diagnostic workstation

Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.

Aug 12, 2026Merge Healthcare, Inc.
Medical DeviceUSFDA Devices

Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Model/Catalog Number: Q6 Edge 3 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller

Pride Mobility Products Corp.
FDA DevicesClass II

Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Model/Catalog Number: Q6 Edge 3 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller

If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

Aug 12, 2026Pride Mobility Products Corp.
Medical DeviceUSFDA Devices

Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number: NCOCO6010 Software Version: N/A Product Description: In situ polymerizing peripheral nerve repair device Component: No

TISSIUM SA
FDA DevicesClass II

Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number: NCOCO6010 Software Version: N/A Product Description: In situ polymerizing peripheral nerve repair device Component: No

Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device beyond its validated shelf life may result in perioperative breakage of the device rendering device unusable; worst-case outcome would be revision surgery.

Aug 12, 2026TISSIUM SA
Food & BeverageUSFDA Food

Clover Hill Dairy LLP, Soft Cuajada in Brine, sold in five (5) gallon and two (2) gallon buckets. Unknown information: labeling. Keep refrigerated.

Clover Hill Dairy, LLC
FDA FoodClass I

Clover Hill Dairy LLP, Soft Cuajada in Brine, sold in five (5) gallon and two (2) gallon buckets. Unknown information: labeling. Keep refrigerated.

Product contaminated with Listeria monocytogenes.

Aug 12, 2026Clover Hill Dairy, LLC
PharmaceuticalUSFDA Drugs

Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1

Sunny Pharmtech Inc.
FDA DrugsClass I

Cyclophosphamide for Injection, USP, 1 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8112-1

Presence of Particulate Matter; identified as stainless steel

Aug 12, 2026Sunny Pharmtech Inc.
Medical DeviceUSFDA Devices

GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system

GE Medical Systems Information Technologies Inc
FDA DevicesClass II

GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system

A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed patient alarms, and/or access to Protected Health Information (PHI).

Aug 12, 2026GE Medical Systems Information Technologies Inc
Medical DeviceUSFDA Devices

Brand Name: U2 Total Knee System Product Name: Femoral valgus offset adaptor, 2mm, 4mm, 6mm, left and Femoral valgus offset adaptor, 2mm, 4mm, 6mm, right Model/Catalog Number: 9323-5335, 9323-5337, 9323-5339 and 9323-5336, 9323-5338, 9323-5340 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No

United Orthopedic Corp.
FDA DevicesClass II

Brand Name: U2 Total Knee System Product Name: Femoral valgus offset adaptor, 2mm, 4mm, 6mm, left and Femoral valgus offset adaptor, 2mm, 4mm, 6mm, right Model/Catalog Number: 9323-5335, 9323-5337, 9323-5339 and 9323-5336, 9323-5338, 9323-5340 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No

Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.

Aug 12, 2026United Orthopedic Corp.
Safety AlertUSRSS Feed

Henkel Corp. Announces a Nationwide Recall of Schwarzkopf Professional Osis Grip 6.76 fl. Oz/200 ml Due to Packaging Imperfection

Unknown Firm
RSS FeedGeneral Alert

Henkel Corp. Announces a Nationwide Recall of Schwarzkopf Professional Osis Grip 6.76 fl. Oz/200 ml Due to Packaging Imperfection

Aug 11, 2026
Safety AlertUSRSS Feed

Lidl US Recalls Vitasia Asian Style Wok Spice Mix Due to Potential Salmonella Contamination

Unknown Firm
RSS FeedGeneral Alert

Lidl US Recalls Vitasia Asian Style Wok Spice Mix Due to Potential Salmonella Contamination

Aug 11, 2026
Safety AlertUSRSS Feed

Recall of Jalapeno Avocado Dressing Because of Possible Health Risk

Unknown Firm
RSS FeedGeneral Alert

Recall of Jalapeno Avocado Dressing Because of Possible Health Risk

Aug 11, 2026
Safety AlertUSRSS Feed

Frankie's Organic Issues Allergy Alert on Undeclared Milk in Frankie’s Organic Plant-Based Vegan Cheddar Puffs

Unknown Firm
RSS FeedGeneral Alert

Frankie's Organic Issues Allergy Alert on Undeclared Milk in Frankie’s Organic Plant-Based Vegan Cheddar Puffs

Aug 11, 2026
Vehicle RecallUSNHTSA

Blue Bird Body Company - Damaged Wiring May Disrupt Critical Safety Functions

Blue Bird Body Company
NHTSAELECTRICAL SYSTEM

Blue Bird Body Company - Damaged Wiring May Disrupt Critical Safety Functions

An electrical short can cause a disruption to safety functions such as a loss of rear lighting or instrument panel warning lights, increasing the risk of a crash.

Aug 10, 2026Blue Bird Body Company
Vehicle RecallUSNHTSA

Blue Bird Body Company - Damaged Wiring May Disrupt Critical Safety Functions

Blue Bird Body Company
NHTSAELECTRICAL SYSTEM

Blue Bird Body Company - Damaged Wiring May Disrupt Critical Safety Functions

An electrical short can cause a disruption to safety functions such as a loss of rear lighting or instrument panel warning lights, increasing the risk of a crash.

Aug 10, 2026Blue Bird Body Company
Vehicle RecallUSNHTSA

Marion Body Works Inc. - Touch Screen Display May Fail

Marion Body Works Inc.
NHTSAEQUIPMENT

Marion Body Works Inc. - Touch Screen Display May Fail

A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing the risk of injury.

Aug 10, 2026Marion Body Works Inc.

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