Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,288 results
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026257 - FORD

Seats And Restraints

Jun 10, 2026TC
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026260 - GENERAL MOTORS

Powertrain

Jun 10, 2026TC
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026262 - VOLVO TRUCKS

Wheels

Jun 10, 2026TC
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026265 - MACK

Wheels

Jun 10, 2026TC
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026271 - FIAT CHRYSLER AUTOMOBILES

Steering

Jun 10, 2026TC
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026272 - FIAT CHRYSLER AUTOMOBILES

High Voltage

Jun 10, 2026TC
Pharmaceutical
FDA DrugsClass II

GOODSENSE Extra Strength, Antacid TABLETS, Calcium Carbonate 750 mg, 96 Chewable...

Presence of foreign substance: small metallic particles in chewable tablets.

Jun 10, 2026Guardian Drug Co. Inc.
Pharmaceutical
FDA DrugsClass III

Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Via...

Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan

Jun 10, 2026Eugia US LLC
Food & Beverage
FDA FoodClass III

UPC 29502200000 Ready Meals BOWL GRAIN SALMON QUINOA LENTIL SS COLD This i...

Contains statement does not declare Salmon

Jun 10, 2026Albertsons Companies LLC
Food & Beverage
FDA FoodClass II

UPC 22655200000 CAKE CARROT 8IN 2-Layer UPC 27813200000 CAKE ...

Contains statement does not declare pecan or walnut.

Jun 10, 2026Albertsons Companies LLC
Food & Beverage
FDA FoodClass II

UPC 27841000000 Ready Meals TRAY BRIE & BLEU CHEESE LARGE This is ...

Contains statement does not declare Almond

Jun 10, 2026Albertsons Companies LLC
Medical Device
FDA DevicesClass I

BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, ...

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

Jun 10, 2026Becton Dickinson & Company
Food & Beverage
FDA FoodClass I

Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per ...

Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination

Jun 10, 2026The Coffee Connexion Co., Inc
Food & Beverage
FDA FoodClass III

UPC 23070400000 SHRIMP SKEWER MEDIUM RAW CILANTRO LIME This is Albertson's st...

Contains statement does not declare Shrimp.

Jun 10, 2026Albertsons Companies LLC
Food & Beverage
FDA FoodClass III

UPC 23044100000 SHRIMP P&D CAJUN SEASONED This is Albertson's store-made i...

Contains statement does not declare Shrimp.

Jun 10, 2026Albertsons Companies LLC
Medical Device
FDA DevicesClass I

Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004

Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or readily visible and the devices therefore remained in service. More specifically, drops or jarring on a hard surface can cause the touchscreen input cable to loosen, resulting in unintended touchscreen behavior on the LVP, including random screen touches and/or lack of screen responsiveness to user input. Under the reported failure condition, unintended touch inputs may register at arbitrary screen locations without user interaction. These inputs occur intermittently and without a predictable pattern.

Jun 10, 2026Fresenius Kabi USA, LLC
Medical Device
FDA DevicesClass I

Spinocan Spinal Needle procedure kits: Material Description (Material Number):...

These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.

Jun 10, 2026B Braun Medical Inc
Medical Device
FDA DevicesClass II

ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system

During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-frame acquisitions. Despite the reported x-ray dose showing 0, an actual x-ray dose is applied to the patient.

Jun 10, 2026Siemens Medical Solutions USA, Inc
Medical Device
FDA DevicesClass I

BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, ...

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

Jun 10, 2026Becton Dickinson & Company
Medical Device
FDA DevicesClass II

The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: L...

Potential for the Cassette Loading Lever to break.

Jun 10, 2026Fresenius Kabi USA, LLC
Medical Device
FDA DevicesClass II

Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsu...

3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.

Jun 10, 2026SSC- Surgical Specialties Corporation
Medical Device
FDA DevicesClass II

Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF: ...

Temperature probe devices lack FDA clearance.

Jun 10, 2026Covidien LLC
Medical Device
FDA DevicesClass I

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL,...

This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

Jun 10, 2026Becton Dickinson & Company
Pharmaceutical
FDA DrugsClass II

Niacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles, Rx Only, Distr...

Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.

Jun 10, 2026Lannett Company Inc.
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