Verbraucherprodukte Recalls

Zinus Metal Bunk Beds recalled due to fall and injury hazards

Naderi Traditional Cookie 210g

The recall is due to the potential presence of an undeclared allergen (peanut).

CareLink Personal Software and CareLink System

A software defect in CareLink Uploader Build 3.1.2 to 3.1.5, may lead to data uploads to the CareLink Personal and CareLink system software being affected by RF interference from surrounding equipment and result in the following: 1. The report may be missing all basal rates that are programmed in the device, and the 24-hour basal total will appear to be incorrectly blank. 2. The report may only display certain programmed basal rates and some other basal rates that are programmed in the device may be missing from the report. This will result in a miscalculation on the Device Settings report of the 24 -hour basal total. Actual delivered insulin calculations in all reports are not impacted, including total daily dose and total basal delivery.

Oxford Partial Knee System Fixed Lateral Tibial Construct, Right-Cemented, E3 (2020-12-02)

Medical devices

Authorization of Bamlanivimab with English-only Labels for Use in Relation to the COVID-19 Pandemic

COVID - Product safety

Kokkadens Cakes & Bakes brand Cakes recalled due to undeclared egg

Egg

Non-Medical Foldable KN95 - Non-Sterile KN95 (2020-12-09)

COVID - Medical devices

EMBLEM S-ICD PULSE GENERATOR & EMBLEM MRI S-ICD PG (2020-12-03)

Medical devices

EMBLEM S-ICD PULSE GENERATOR & EMBLEM MRI S-ICD PG (2020-12-03)

Medical devices

EMBLEM S-ICD SUBCUTANEOUS ELECTRODE (2020-12-03)

Medical devices

Multiple Sterile Zimmer Biomet Products (2020-12-02)

Medical devices

ELONGATED FACE MASKS (2020-12-03)

Medical devices

Biomeme Go Mobile Smartphone Application (2020-10-26)

Medical devices

Cobas z 480 (2020-12-08)

Medical devices

Sysmex Automated Blood Coagulation Analyzers (2020-09-10)

Medical devices

President's Choice brand spread and dip products recalled due to spoilage

Can-Am Off-Road Screw Jack recalled due to injury hazard

Otis Elevator Company Recalls to Inspect Private Residence Elevators Due to Entrapment Hazard; Risk of Serious Injury or Death to Young Children

Children can become entrapped in the space between the exterior landing (hoistway) door and the interior elevator car door or gate, and suffer serious injuries or death when the elevator is called to another floor.

Payot Paris Sunny Magic Mousse à Bronzer recalled due to missing hazard labelling

BRP Recalls Can-Am Screw Jacks Due to Crush Hazard

The screw jack can collapse and cause the lifted vehicle to fall on a person, posing a crush hazard that can result in severe injury or death.

Aurora Orange Handsmoke Distress Flare

Smoke may vent from both the top and the bottom of the product, instead of venting just from the top, causing the handle of the product to become hot.

Micro Shot Blasters by Nerf

Affected product does not comply with the requirements of the mandatory standard 'Consumer Protection Notice No.16 of 2010 - Consumer Product Safety Standard: Children’s Projectile Toys'. The warning text 'WARNING: Do not aim at eyes or face' was in Spanish and Portuguese instead of English.

White Knight Antibacterial Hand Sanitiser 500mL and White Knight Sweet Berry Antibacterial Hand Sanitiser 500mL

The product contains less than the 70% or 75% alcohol content that is detailed on the product's label.

Graco Recalls Inclined Sleeper Accessory Included with Four Models of Playards to Prevent Risk of Suffocation

Infant fatalities have been reported with other manufacturers' inclined sleep products, after infants rolled from their back to their stomach or side while unrestrained, or under other circumstances.