Safety Recall Directory
Browse and filter the latest official safety alerts globally.
(BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099
Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.
Transport Canada Recall - 2026243 - DAIMLERCHRYSLER COMMERCIAL BUSES
Lights And Instruments
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.
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.
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.
IntelliCuff®
Performance
Dexcom G7 Sensor 1 Pack
Unauthorised device
giant eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps, Net Wt ...
Products were made with recalled California Dairies milk powder due to Salmonella.
ARTIS Icono Ceiling, Floor and Biplane Systems
Performance
IceMan CLASSIC3™
Performance
GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF...
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).
BD Canada ChloraPrep product recall; Sterility concerns
Product quality
Transport Canada Recall - 2026236 - YAMAHA
Lights And Instruments
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.
Oster Kool-Lube and Oster Blade Wash recalled due to improper labelling
Labelling and packaging
Aston Martin The Americas - Brake Master Cylinder Seal May Deform
Brakes that overheat increase the risk of a fire.
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.
Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimul...
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.
Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimul...
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.
sans marque - ti guémené
présence de listeria monocytogenes.
PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Steril...
Failed Stability Specifications
Transport Canada Recall - 2026249 - BENTLEY
Powertrain
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.
Transport Canada Recall - 2026229 - FORD
Structure