Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,115 results
Safety AlertCanadaHealth Canada

Dexcom G7 Sensor 1 Pack

Medical devices
Health CanadaType II

Dexcom G7 Sensor 1 Pack

Unauthorised device

Jun 3, 2026Medical devices
Safety AlertCanadaHealth Canada

ARTIS Icono Ceiling, Floor and Biplane Systems

Medical devices
Health CanadaType II

ARTIS Icono Ceiling, Floor and Biplane Systems

Performance

Jun 3, 2026Medical devices
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026236 - YAMAHA

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026236 - YAMAHA

Lights And Instruments

Jun 3, 2026TC
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026243 - DAIMLERCHRYSLER COMMERCIAL BUSES

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026243 - DAIMLERCHRYSLER COMMERCIAL BUSES

Lights And Instruments

Jun 3, 2026TC
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026239 - TESLA

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026239 - TESLA

Label

Jun 3, 2026TC
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026248 - ABC COMPANIES

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026248 - ABC COMPANIES

Structure

Jun 3, 2026TC
Safety AlertCanadaHealth Canada

​​Oster Kool-Lube and Oster Blade Wash​ recalled due to improper labelling

Consumer product safety
Health CanadaGeneral Alert

​​Oster Kool-Lube and Oster Blade Wash​ recalled due to improper labelling

Labelling and packaging

Jun 3, 2026Consumer product safety
Safety AlertCanadaHealth Canada

IceMan CLASSIC3™

Medical devices
Health CanadaType II

IceMan CLASSIC3™

Performance

Jun 3, 2026Medical devices
Safety AlertCanadaHealth Canada

BD Canada ChloraPrep product recall; Sterility concerns

Drugs and health products
Health CanadaType II

BD Canada ChloraPrep product recall; Sterility concerns

Product quality

Jun 3, 2026Drugs and health products
Safety AlertCanadaHealth Canada

IntelliCuff®

Medical devices
Health CanadaType II

IntelliCuff®

Performance

Jun 3, 2026Medical devices
Vehicle RecallUSNHTSA

Jayco, Inc. - False Taillight Warning Light on Instrument Panel Display/FMVSS 101

Jayco, Inc.
NHTSAELECTRICAL SYSTEM

Jayco, Inc. - False Taillight Warning Light on Instrument Panel Display/FMVSS 101

The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.

Jun 3, 2026Jayco, Inc.
Food & BeverageUSFDA Food

Wawa Diet Lemonade Pint (16oz), Plastic bottle

Wawa Beverage Company
FDA FoodClass I

Wawa Diet Lemonade Pint (16oz), Plastic bottle

Undeclared Milk Allergen,

Jun 3, 2026Wawa Beverage Company
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026246 - GENERAL MOTORS

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026246 - GENERAL MOTORS

Airbag

Jun 3, 2026TC
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026229 - FORD

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026229 - FORD

Structure

Jun 3, 2026TC
Safety AlertAustraliaAustralia Products

Pool noodle (sold on TEMU)

Unknown Firm
Pool noodle (sold on TEMU)
Australia ProductsInflatable toys...

Pool noodle (sold on TEMU)

This product does not comply with the aquatic toys mandatory standard . The product does not display the permanent warnings as required by the mandatory standard.

Jun 3, 2026
Safety AlertAustraliaAustralia Products

Stainless King™ Food Jars

Unknown Firm
Stainless King™ Food Jars
Australia ProductsKitchenware and...

Stainless King™ Food Jars

The stopper on affected products does not have a pressure release valve. Pressure may build up inside the container and may cause the stopper beneath the lid to eject forcefully when opened.

Jun 3, 2026
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026244 - FIAT CHRYSLER AUTOMOBILES

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026244 - FIAT CHRYSLER AUTOMOBILES

Airbag

Jun 3, 2026TC
Medical DeviceUSFDA Devices

RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U 28-N4-32-164-28U 28-N4-32-164-32U 28-N4-32-209-28U 28-N4-32-209-32U 28-N4-32-259-32U 28-N4-34-109-34U 28-N4-34-154-30U 28-N4-34-154-34U 28-N4-34-209-30U 28-N4-34-209-34U 28-N4-34-259-34U 28-N4-36-109-36U 28-N4-36-154-32U 28-N4-36-154-36U 28-N4-36-199-32U 28-N4-36-199-36U 28-N4-36-259-36U 28-N4-38-109-38U 28-N4-38-154-34U 28-N4-38-154-38U 28-N4-38-199-34U 28-N4-38-199-38U 28-N4-38-259-38U 28-N4-40-114-40U 28-N4-40-154-36U 28-N4-40-154-40U 28-N4-40-204-36U 28-N4-40-204-40U 28-N4-40-259-40U 28-N4-42-114-42U 28-N4-42-159-38U 28-N4-42-159-42U 28-N4-42-204-38U 28-N4-42-204-42U 28-N4-42-259-42U 28-N4-44-114-44U 28-N4-44-164-40U 28-N4-44-164-44U 28-N4-44-209-40U 28-N4-44-209-44U 28-N4-44-259-40U 28-N4-44-259-44U 28-N4-46-114-46U 28-N4-46-164-42U 28-N4-46-164-46U 28-N4-46-209-42U 28-N4-46-209-46U 28-N4-46-259-42U

Bolton Medical Inc.
FDA DevicesClass I

RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U 28-N4-32-164-28U 28-N4-32-164-32U 28-N4-32-209-28U 28-N4-32-209-32U 28-N4-32-259-32U 28-N4-34-109-34U 28-N4-34-154-30U 28-N4-34-154-34U 28-N4-34-209-30U 28-N4-34-209-34U 28-N4-34-259-34U 28-N4-36-109-36U 28-N4-36-154-32U 28-N4-36-154-36U 28-N4-36-199-32U 28-N4-36-199-36U 28-N4-36-259-36U 28-N4-38-109-38U 28-N4-38-154-34U 28-N4-38-154-38U 28-N4-38-199-34U 28-N4-38-199-38U 28-N4-38-259-38U 28-N4-40-114-40U 28-N4-40-154-36U 28-N4-40-154-40U 28-N4-40-204-36U 28-N4-40-204-40U 28-N4-40-259-40U 28-N4-42-114-42U 28-N4-42-159-38U 28-N4-42-159-42U 28-N4-42-204-38U 28-N4-42-204-42U 28-N4-42-259-42U 28-N4-44-114-44U 28-N4-44-164-40U 28-N4-44-164-44U 28-N4-44-209-40U 28-N4-44-209-44U 28-N4-44-259-40U 28-N4-44-259-44U 28-N4-46-114-46U 28-N4-46-164-42U 28-N4-46-164-46U 28-N4-46-209-42U 28-N4-46-209-46U 28-N4-46-259-42U

Labeling update concerning proximal clasp disconnection from the outer control tube which may prevent stent graft from being released from the delivery system.

Jun 3, 2026Bolton Medical Inc.
Food & BeverageUSFDA Food

giant eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps, Net Wt 7.33 oz. Shipping Case: 12 ct - 7.33 oz Bags Net Weight: 5.49 lbs. Legacy Bakehouse, LLC, Waukesha WI 53186.

Legacy Bakehouse LLC
FDA FoodClass I

giant eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps, Net Wt 7.33 oz. Shipping Case: 12 ct - 7.33 oz Bags Net Weight: 5.49 lbs. Legacy Bakehouse, LLC, Waukesha WI 53186.

Products were made with recalled California Dairies milk powder due to Salmonella.

Jun 3, 2026Legacy Bakehouse LLC
Medical DeviceUSFDA Devices

Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)

O&M HALYARD INC
FDA DevicesClass II

Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)

Nitrile Exam Glove failed to meet specifications chemical permeation performance.

Jun 3, 2026O&M HALYARD INC
Vehicle RecallUSNHTSA

Jayco, Inc. - False Taillight Warning Light on Instrument Panel Display/FMVSS 101

Jayco, Inc.
NHTSAELECTRICAL SYSTEM

Jayco, Inc. - False Taillight Warning Light on Instrument Panel Display/FMVSS 101

The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.

Jun 3, 2026Jayco, Inc.
Medical DeviceUSFDA Devices

GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

GE Medical Systems Information Technologies Inc
FDA DevicesClass II

GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).

Jun 3, 2026GE Medical Systems Information Technologies Inc
Medical DeviceUSFDA Devices

Automated Impella Controller (AIC); Product Code: 0042-0000-US;

Abiomed, Inc.
FDA DevicesClass I

Automated Impella Controller (AIC); Product Code: 0042-0000-US;

A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns. These hardware updates have been implemented through Abiomed s servicing process; therefore, AICs that have not received service are pending these updates. Issue 1: The proximity of the internal Video Graphics Array cable to the Digital Signal Processor chipset on the Impellatronic printed circuit assembly could potentially result in Electrostatic Discharge coupling into the Digital Signal Processor which may interrupt motor controls. Issue 2: There is a potential for the Compact Flash Memory Card dislodgement due to external applied forces, which could result in AIC startup failures and data logging issues. Issue 3: Improper routing of the fan wire within the AIC could lead to fan wire damage, which may result in console boot-up failure. Issue 4: Potential capacitor related issues on the Power Battery Manager, including the potential for the capacitors to cause pump stop, purge stop, and/or single fan fuse failures.

Jun 3, 2026Abiomed, Inc.
Medical DeviceUSFDA Devices

GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

GE Medical Systems Information Technologies Inc
FDA DevicesClass II

GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).

Jun 3, 2026GE Medical Systems Information Technologies Inc

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