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Food & Beverage
FDA FoodClass II

001165: Standard Pasteurized Donor Human Milk; 100 mL bottles 001198: Pediatric ...

Product is potentially contaminated with foreign material (plastic particles).

Jun 10, 2026University of California Health Milk Bank
Food & Beverage
FDA FoodClass II

UPC 21600500000 READY MEALS SALAD PREMIUM BROCCOLI SS This is A...

Contains statement does not declare Cashew

Jun 10, 2026Albertsons Companies LLC
Pharmaceutical
FDA DrugsClass II

CAREone, EXTRA STRENGTH CALCIUM ANTACID, Calcium Carbonate 750 mg, 96 chewable T...

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

Jun 10, 2026Guardian Drug Co. Inc.
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026275 - HONDA

Structure

Jun 10, 2026TC
Pharmaceutical
FDA DrugsClass II

TopCare health, ULTRA STRENGTH, Antacid Tablets, CALCIUM CARBONATE 1000mg, 72 CH...

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

Jun 10, 2026Guardian Drug Co. Inc.
Medical Device
FDA DevicesClass II

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the product solution and the stainless steel spring and may result in visible discoloration and the presence of trace levels of metallic elements (including iron, chromium, and nickel) in the solution during use.

Jun 10, 2026Oculus Technologies of Mexico, S.A. de C.V.
Medical Device
FDA DevicesClass II

COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI cod...

Due to customer complaint regarding incorrect display box labeling.

Jun 10, 2026Covidien LLC
Food & Beverage
FDA FoodClass I

Raw Shelled Peanuts (Runner Type) 2,200 lb. Poly Tote Bags and 50kg Poly Bags

Undeclared Tree Nut Allergen

Jun 10, 2026Wilco Peanut Co
Food & Beverage
FDA FoodClass II

UPC 23114800000 SEAFOOD SALAD IMITATION CAJUN CRAB This is Albertson's st...

Contains statement does not declare Crab and Pollock

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

White Cheddar Seasoning packaged in the following sized containers: 1. Net Wt...

Products may be potentially contaminated with Salmonella.

Jun 10, 2026JCB Flavors, LLC
Medical Device
FDA DevicesClass II

BD Pyxis MedStation ES Tower REF: 352 Medication cabinet

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

Jun 10, 2026CareFusion 303, Inc.
Food & Beverage
FDA FoodClass II

UPC 21243500000 KITCHEN SANDWICH ITALIAN SUPER SUB SS COLD This is A...

Contains statement does not declare Pistachio

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

BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 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 III

UPC 25800800000 POP DOTS COCO & HAZELNUT 6CT This is Alber...

Contains statement does not declare hazelnut

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

Brand Name: B. BRAUN MEDICAL INC. Product Name: LYNDON B JOHNSON HOSPITAL SPINA...

B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.

Jun 10, 2026B Braun Medical Inc
Food & Beverage
FDA FoodClass II

UPC 22418000000 Platter Catering Loaf Cake Slice. Th...

Contains statement does not declare Walnut.

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

Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used ...

Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock cannot be reliably engaged with the CFCV snap interface. In instances where engagement is achieved through applied force, the connection is unstable, and the stopcock may disengage before or during contrast injection, leading to procedure interruption.

Jun 10, 2026Bayer Medical Care, Inc.
Food & Beverage
FDA FoodClass II

UPC 21478000000 Ready Meals SALAD FRESH BERRY & SWEET CHILI Salmon SS This i...

Contains statement does not declare Salmon and Walnut

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

BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

Jun 10, 2026CareFusion 303, Inc.
Food & Beverage
FDA FoodClass II

UPC 25811100000 CAKE RASPBERRY MOON 8IN 2-layer. This is Albertson's store-made...

Contains statement does not declare Almond.

Jun 10, 2026Albertsons Companies LLC
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.
Medical Device
FDA DevicesClass II

CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3

Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer head can result in charring or discoloration of thermal printer paper. Ignition of the paper could potentially result in serious thermal injury.

Jun 10, 2026GE Medical Systems Information Technologies Inc
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
Medical Device
FDA DevicesClass II

Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2....

During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.

Jun 10, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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