Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,115 results
Vehicle RecallUSNHTSA

BMW of North America, LLC - Loss of Rear Wheel Power from Driveshaft Damage

BMW of North America, LLC
NHTSAPOWER TRAIN

BMW of North America, LLC - Loss of Rear Wheel Power from Driveshaft Damage

An unexpected loss of drive power can increase the risk of a crash. In addition, a damaged driveshaft can result in a vehicle rollaway if the parking brake is not applied, increasing the risk of a crash or injury.

Aug 12, 2026BMW of North America, LLC
Food & BeverageAustraliaFSANZ Food

Edesia Enterprises Pty Ltd T/A noosa GOURMET - Brioche Rolls - 320g

Edesia Enterprises Pty Ltd T/A noosa GOURMET
Edesia Enterprises Pty Ltd T/A noosa GOURMET - Brioche Rolls - 320g
FSANZ FoodFood Safety

Edesia Enterprises Pty Ltd T/A noosa GOURMET - Brioche Rolls - 320g

The presence of undeclared allergens (milk and egg).

Aug 12, 2026Edesia Enterprises Pty Ltd T/A noosa GOURMET
Food & BeverageFranceRappelConso

leroy - filet de truite fumé prétranché

leroy
RappelConsovolontaire (san...

leroy - filet de truite fumé prétranché

des analyses ont mis en évidence la présence de listeria monocytogenes dans ce produit.

Aug 12, 2026leroy
Food & BeverageFranceRappelConso

paturages comtois - brie

paturages comtois
RappelConsovolontaire (san...

paturages comtois - brie

rappel préventif suite à détection listeria dans un autre lot fabriqué le même jour

Aug 12, 2026paturages comtois
Food & BeverageFranceRappelConso

sans marque / vendus au rayon traditionnel - crevettes entières cuites réfrigérées élevées à madagscar - calibre 10/20 sx

sans marque / vendus au rayon traditionnel
RappelConsovolontaire (san...

sans marque / vendus au rayon traditionnel - crevettes entières cuites réfrigérées élevées à madagscar - calibre 10/20 sx

présence de listeria monocytogenes détectée lors d'une analyse microbilogique.

Aug 12, 2026sans marque / vendus au rayon traditionnel
Food & BeverageFranceRappelConso

manicamp - manicamp

manicamp
RappelConsovolontaire (san...

manicamp - manicamp

présence potentielle de listéria monocytogenes

Aug 12, 2026manicamp
Medical DeviceUSFDA Devices

Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product Description: Intramedullary Bone Saw Blade Assembly 15mm

Biomet, Inc.
FDA DevicesClass II

Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475635 Product Description: Intramedullary Bone Saw Blade Assembly 15mm

Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.

Aug 12, 2026Biomet, Inc.
Medical DeviceUSFDA Devices

Brand Name: Quantum Rehab Product Name: 4Front Model/Catalog Number: 4Front 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: 4Front Model/Catalog Number: 4Front 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: Quantum 1450 Model/Catalog Number: Quantum 1450 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 1450 Model/Catalog Number: Quantum 1450 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

INFINION CX LEAD KIT, 50CM, Model: SC-2317-50, Material: M365SC2317500; INFINION CX LEAD KIT, 70CM, Model: SC-2317-70, Material: M365SC2317700. part of the Boston Scientific Spinal Cord Stimulator (SCS) Systems.

Boston Scientific Neuromodulation Corporation
FDA DevicesClass I

INFINION CX LEAD KIT, 50CM, Model: SC-2317-50, Material: M365SC2317500; INFINION CX LEAD KIT, 70CM, Model: SC-2317-70, Material: M365SC2317700. part of the Boston Scientific Spinal Cord Stimulator (SCS) Systems.

Spinal cord stimulation system lead body may be exposed to stress at the anchor site. This may result in high impedance measurements or lead fractures, which may lead to inadequate stimulation, additional intervention, including lead explant and replacement.

Aug 12, 2026Boston Scientific Neuromodulation Corporation
Safety AlertAustraliaAustralia Products

Nevenka Baby pull string giraffe toy

Unknown Firm
Nevenka Baby pull string giraffe toy
Australia ProductsRattles and toy...

Nevenka Baby pull string giraffe toy

The product does not comply with the mandatory standard for toys for children up to and including 36 months of age . The product’s silicone pull strings that are too long and can reach the back of a child's throat causing choking or asphyxiation. The feet on the ends of the silicone pull strings can detach from the product and cause a child to choke if they place them in their mouth.

Aug 12, 2026
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

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
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: 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

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 & BeverageFranceRappelConso

qualiko - filet de polulet nature

qualiko
RappelConsovolontaire (san...

qualiko - filet de polulet nature

blanc poulet congele teste positif a la salmonelle

Aug 12, 2026qualiko
Medical DeviceUSFDA Devices

Brand Name: COAPTIUM Connect Product Name: COAPTIUM Connect Model/Catalog Number: NCOCO1510 Software Version: N/A Product Description: In situ polymerizing peripheral nerve repair device Component: N/A

TISSIUM SA
FDA DevicesClass II

Brand Name: COAPTIUM Connect Product Name: COAPTIUM Connect Model/Catalog Number: NCOCO1510 Software Version: N/A Product Description: In situ polymerizing peripheral nerve repair device Component: N/A

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
Safety AlertUSRSS Feed

Whole Foods Market Announces a Recall of Select Salsas, Guacamole, Pico de Gallo, and Prepared Foods Products Because of Possible Health Risk

Unknown Firm
RSS FeedGeneral Alert

Whole Foods Market Announces a Recall of Select Salsas, Guacamole, Pico de Gallo, and Prepared Foods Products Because of Possible Health Risk

Aug 12, 2026
Vehicle RecallUSNHTSA

Odyne Systems, LLC - High Voltage Battery May Fail and Cause Fire

Odyne Systems, LLC
NHTSAELECTRICAL SYSTEM

Odyne Systems, LLC - High Voltage Battery May Fail and Cause Fire

Battery failure can also increase the risk of a fire.

Aug 12, 2026Odyne Systems, 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
Food & BeverageUSFDA Food

Clover Hill Dairy LLP, Flavored Cheese (horseradish). Sold in approximate 1/2-lb, 1-lb, 2.5-lb, 5-lb, and 40-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, Flavored Cheese (horseradish). Sold in approximate 1/2-lb, 1-lb, 2.5-lb, 5-lb, and 40-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
Food & BeverageUSFDA Food

Ultimate Mother's Day Wangshin Doenjang Aged 3 Years 9 oz. Korean Traditional Premium Soybean Paste UPC: 8 809897 940169

JINA F&C
FDA FoodClass II

Ultimate Mother's Day Wangshin Doenjang Aged 3 Years 9 oz. Korean Traditional Premium Soybean Paste UPC: 8 809897 940169

Product label allergen "contains" statement does not include anchovy(fish)

Aug 12, 2026JINA F&C
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

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