Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,313 results
Medical Device
FDA DevicesClass I

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, la...

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

Jun 3, 2026Medline Industries, LP
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026246 - GENERAL MOTORS

Airbag

Jun 3, 2026TC
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026244 - FIAT CHRYSLER AUTOMOBILES

Airbag

Jun 3, 2026TC
Vehicle
NHTSASERVICE BRAKES,...

Aston Martin The Americas - Brake Master Cylinder Seal May Deform

Brakes that overheat increase the risk of a fire.

Jun 3, 2026Aston Martin The Americas
Medical Device
FDA DevicesClass I

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, la...

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

Jun 3, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS),...

Nitrile Exam Glove failed to meet specifications chemical permeation performance.

Jun 3, 2026O&M HALYARD INC
Food & Beverage
Germany BVLGeneral Alert

Basilikum gerebelt, 15 Gramm

Krankheitserreger

Jun 3, 2026Lieferant TSI Consumer Goods Gesellschaft mit beschränkter Haftung, Südring 26, 27404 Zeven
Medical Device
FDA DevicesClass II

Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003...

It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an HDD may, depending on the specific system PC in which the affected HDD is installed, result in loss of imaging functionality. Additionally, in Allura systems, this may lead to loss of motorized movement, or loss of data. In some cases, a system restart may temporarily restore functionality.

Jun 3, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
sans marque - spaghetti carbonara, panzerotti aux cêpes et champignons, croissan...
RappelConsovolontaire (san...

sans marque - spaghetti carbonara, panzerotti aux cêpes et champignons, croissan...

présence de listeria

Jun 3, 2026sans marque
Food & Beverage
FDA FoodClass I

Butter Parsley Bagel Crisps, Item Number 18490, Net Weight: 10 lbs. Legacy Bak...

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

Jun 3, 2026Legacy Bakehouse LLC
Vehicle
NHTSAELECTRICAL SYSTEM

Jayco, Inc. - False Taillight Warning Light on Instrument Panel Display/FMVSS 10...

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.
grand frais / fresh / mon-marché.fr - brisures de saumon fumé 150g
RappelConsovolontaire (san...

grand frais / fresh / mon-marché.fr - brisures de saumon fumé 150g

détection listeria monocytogenes

Jun 3, 2026grand frais / fresh / mon-marché.fr
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026252 - BRINKLEY RV

Suspension

Jun 3, 2026TC
Medical Device
FDA DevicesClass I

RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-3...

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.
Medical Device
FDA DevicesClass I

Automated Impella Controller (AIC) with the below product descriptions and corre...

Retrospective submission for following issues identified: 1. Alarm failures, power-path faults, electrical-short risks, and inaccurate motor-current sensing were identified in certain AIC consoles. 2. There is improper alignment between the purge cassette and the motor drive in the AIC. This can result in a piston block event and lead to the inability to complete priming of the purge system, requiring the user to switch to backup AIC console.

Jun 3, 2026Abiomed, Inc.
Pharmaceutical
FDA DrugsClass III

PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Steril...

Failed Stability Specifications

Jun 3, 2026AbbVie Inc.
Food & Beverage
FDA FoodClass I

Wawa Fruit Punch Pint (16oz), Plastic bottle

Undeclared Milk Allergen,

Jun 3, 2026Wawa Beverage Company
Medical Device
FDA DevicesClass II

GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603...

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 Device
FDA DevicesClass I

Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, la...

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

Jun 3, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Pro...

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 Device
FDA DevicesClass II

Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, ...

It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an HDD may, depending on the specific system PC in which the affected HDD is installed, result in loss of imaging functionality. Additionally, in Allura systems, this may lead to loss of motorized movement, or loss of data. In some cases, a system restart may temporarily restore functionality.

Jun 3, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Vehicle
NHTSAELECTRICAL SYSTEM

Jayco, Inc. - False Taillight Warning Light on Instrument Panel Display/FMVSS 10...

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.
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
Pharmaceutical
FDA DrugsClass III

Nicotine Transdermal System Patch, 14 mg, 14 patches per box, Aveva, Distributed...

Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of individual units.

Jun 3, 2026AVEVA Drug Delivery Systems, Inc.
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