Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,116 results
Safety AlertCanadaHealth Canada

VITEK® 2 Systems

Medical devices
Health CanadaType II

VITEK® 2 Systems

Performance

Jan 21, 2026Medical devices
Safety AlertCanadaHealth Canada

GE HealthCare Nuclear Medicine Systems

Medical devices
Health CanadaType II

GE HealthCare Nuclear Medicine Systems

Performance

Jan 21, 2026Medical devices
Safety AlertCanadaHealth Canada

PNW Components Loam Pedal Gen 2 bicycle pedals recalled due to fall hazard

Consumer product safety
Health CanadaGeneral Alert

PNW Components Loam Pedal Gen 2 bicycle pedals recalled due to fall hazard

Fall hazard

Jan 21, 2026Consumer product safety
Safety AlertCanadaHealth Canada

ANNQUAN Brand Power Strips recalled due to fire hazard

Consumer product safety
Health CanadaGeneral Alert

ANNQUAN Brand Power Strips recalled due to fire hazard

Fire hazard

Jan 21, 2026Consumer product safety
Safety AlertCanadaHealth Canada

Nûby IcyBite™ Keys Teethers recalled due to microbial contamination

Consumer product safety
Health CanadaGeneral Alert

Nûby IcyBite™ Keys Teethers recalled due to microbial contamination

Microbial hazard

Jan 21, 2026Consumer product safety
Safety AlertCanadaHealth Canada

Veggie Paradise brand Vegan Ham recalled due to undeclared wheat

CFIA
Health CanadaClass 2

Veggie Paradise brand Vegan Ham recalled due to undeclared wheat

Wheat

Jan 21, 2026CFIA
Safety AlertCanadaHealth Canada

Ventilator Circuit For Non-Invasive Ventilation

Medical devices
Health CanadaType II

Ventilator Circuit For Non-Invasive Ventilation

Labelling and packaging

Jan 21, 2026Medical devices
Safety AlertCanadaHealth Canada

SAFE-T-FILL®

Medical devices
Health CanadaType II

SAFE-T-FILL®

Performance

Jan 21, 2026Medical devices
Safety AlertCanadaHealth Canada

Hemodialysis Opening (Hemodialyse Ouverture) Packs

Medical devices
Health CanadaType II

Hemodialysis Opening (Hemodialyse Ouverture) Packs

Performance

Jan 21, 2026Medical devices
Safety AlertCanadaHealth Canada

PTI brand Besan Chick Pea Flour recalled due to the presence of insects

CFIA
Health CanadaClass 3

PTI brand Besan Chick Pea Flour recalled due to the presence of insects

Extraneous Material

Jan 21, 2026CFIA
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026011 - WINNEBAGO INDUSTRIES

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026011 - WINNEBAGO INDUSTRIES

Electrical

Jan 21, 2026TC
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026012 - LUCID MOTORS, INC.

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026012 - LUCID MOTORS, INC.

Visual System

Jan 21, 2026TC
Medical DeviceUSFDA Devices

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START KIT NS, Medline kit SKU DYKM1980C; 2) (134) L&D IV-START SET, Medline kit SKU DYKM2137B; 3) IV START KIT, Medline kit SKU DYKS1372C; 4) IV START KIT, Medline kit SKU DYNDV1691B; 5) OUTPATIENT 2 TO 5 YEARS, Medline kit SKU DYNDV2464A.

Medline Industries, LP
FDA DevicesClass II

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) IV START KIT NS, Medline kit SKU DYKM1980C; 2) (134) L&D IV-START SET, Medline kit SKU DYKM2137B; 3) IV START KIT, Medline kit SKU DYKS1372C; 4) IV START KIT, Medline kit SKU DYNDV1691B; 5) OUTPATIENT 2 TO 5 YEARS, Medline kit SKU DYNDV2464A.

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Jan 21, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

Allura Xper FD10; Model Number: 722026;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Allura Xper FD10; Model Number: 722026;

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.

Jan 21, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceUSFDA Devices

Allura Xper FD20; Model Number: 722006;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Allura Xper FD20; Model Number: 722006;

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.

Jan 21, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceUSFDA Devices

Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Number: SP001-0026, SP003-0002 Software Version: cSRS module in combination with cMotion module Product Description: GMDN: 40893 Patient positioning device, diagnostic imaging/radiotherapy, laser Component: Not applicable

C-RAD POSITIONING AB
FDA DevicesClass II

Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Number: SP001-0026, SP003-0002 Software Version: cSRS module in combination with cMotion module Product Description: GMDN: 40893 Patient positioning device, diagnostic imaging/radiotherapy, laser Component: Not applicable

Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups. n certain cases, the system may indicate the patient as correctly positioned at the isocenter, even when the isocenter is positioned outside of the indicated tolerance.

Jan 21, 2026C-RAD POSITIONING AB
Medical DeviceUSFDA Devices

Brand Name: PALACOS Product Name: PALACOS R pro 40; PALACOS R pro 80 Model/Catalog Number: 5081286; 5081287 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A

Heraeus Medical GmbH (Dental Division)
FDA DevicesClass II

Brand Name: PALACOS Product Name: PALACOS R pro 40; PALACOS R pro 80 Model/Catalog Number: 5081286; 5081287 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A

increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.

Jan 21, 2026Heraeus Medical GmbH (Dental Division)
Food & BeverageUSFDA Food

2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8

House Of Flavors, Inc.
FDA FoodClass II

2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8

Undeclared soy lecithin

Jan 21, 2026House Of Flavors, Inc.
Safety AlertAustraliaAustralia Products

Pet Gravity LED Nail Clippers

Unknown Firm
Pet Gravity LED Nail Clippers
Australia ProductsButton batteries

Pet Gravity LED Nail Clippers

The nail clippers don’t comply with the mandatory standards for products containing button/coin batteries . The battery isn’t secured, and children could access the button/coin battery. The product is missing warning information about the dangers of button/coin batteries to children what to do when a person suspects someone has swallowed or placed a button/coin battery inside any part of their body.

Jan 21, 2026
Safety AlertAustraliaAustralia Products

Orchard Toys Jungle Heads and Tails card game

Unknown Firm
Orchard Toys Jungle Heads and Tails card game
Australia ProductsGames and puzzles

Orchard Toys Jungle Heads and Tails card game

This product does not comply with the mandatory standard for toys for children up to and including 36 months of age . The elephant playing piece has a small cardboard disc which should have been removed from the nose during the manufacturing process. The disc can separate from the card and become a hazardous small part.

Jan 21, 2026
Medical DeviceUSFDA Devices

FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.

Abbott Diabetes Care, Inc.
FDA DevicesClass I

FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

Jan 21, 2026Abbott Diabetes Care, Inc.
Food & BeverageUSFDA Food

Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case

GUSTO GROUP, INC.
FDA FoodClass II

Shrimp Paste (Klong Kone) 'M' , 16 oz, 24 count , PLastic Jar, 24 packages/ case

Product tested high for lead.

Jan 21, 2026GUSTO GROUP, INC.
Medical DeviceUSFDA Devices

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) OPEN HEART ACCESSORY CDSKit SKU CDS984289O; 2) OPEN HEART CDSKit SKU CDS984355K; 3) BAG A OPEN HEART KITKit SKU DYKM1025D; 4) RR-CABG SUPPLEMENTAL PACKKit SKU DYNJ0394752O; 5) OPEN HEART CDSKit SKU DYNJ902879T; 6) BASIC CARDIAC ANESTHESIAKit SKU DYNJ903523F; 7) OPEN HEART CDSKit SKU DYNJ905557B; 8) AN03 HEART/ANESTHESIA KIT-LFKit SKU PHS972012D.

Medline Industries, LP
FDA DevicesClass II

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) OPEN HEART ACCESSORY CDSKit SKU CDS984289O; 2) OPEN HEART CDSKit SKU CDS984355K; 3) BAG A OPEN HEART KITKit SKU DYKM1025D; 4) RR-CABG SUPPLEMENTAL PACKKit SKU DYNJ0394752O; 5) OPEN HEART CDSKit SKU DYNJ902879T; 6) BASIC CARDIAC ANESTHESIAKit SKU DYNJ903523F; 7) OPEN HEART CDSKit SKU DYNJ905557B; 8) AN03 HEART/ANESTHESIA KIT-LFKit SKU PHS972012D.

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Jan 21, 2026Medline Industries, LP
Vehicle RecallUSNHTSA

Ford Motor Company - Brake Lights May Fail to Illuminate/FMVSS 108

Ford Motor Company
NHTSAEXTERIOR LIGHTING

Ford Motor Company - Brake Lights May Fail to Illuminate/FMVSS 108

Brake lights that do not illuminate properly while driving increase the risk of a crash. In addition, the vehicle may be shifted out of park without the brake pedal applied, increasing the risk of a rollaway and crash.

Jan 21, 2026Ford Motor Company

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