Produits de Consommation Recalls

Auro Pharma Losartan product recall (2021-10-12)

Product safety

One lot of GENIUS Kids and Teens softgel capsules recalled due to possible bacterial contamination

REVOLUTION CT (2021-10-11)

Recall: One lot of Riva-Risperidone 0.25 mg tablets recalled due to a packaging error

Recall: One lot of Riva-Risperidone 0.25 mg tablets recalled due to a packaging error

Expanded Recall: Various JHY Design Tabletop Firepots recalled due to lack of appropriate labelling and hazard information

All Elekta Limited Digital Accelerators (2021-09-17)

Medical devices

Bodyguard pumps (2021-09-16)

Medical devices

EPIQ DIAGNOSTIC ULTRASOUND SYSTEM (2021-09-20)

Medical devices

Vidas products (2021-09-26)

Medical devices

N95 Particulate Respirator (2021-09-15)

Medical devices

Alcohol Antiseptic 80% (v/v) Topical Solution Hand Sanitizer (2021-10-08)

COVID

RUSCH Endotracheal Tube (2021-07-16)

Medical devices

Biomeme SARS-CoV-2 Real-Time RT-PCR Test (2021-07-22)

COVID - Medical devices

Deon Oyster Company Limited brand Atlantic Oysters recalled due to generic E. coli

Microbial contamination

Health Canada suspends licence and requested a recall for PURE75 gel hand sanitizer due to potential serious health risks

General Motors Chevrolet (GMC) Chevrolet Silverado Gen 2 GMT900 Utility Vehicle MY2014

Airbag inflator: As it gets older, a combination of high temperatures and humidity can cause the airbag inflator propellant to degrade. If an affected vehicle is involved in a collision triggering the airbag, the metal inflator housing may explode/rupture under too much internal pressure.

Wooden Baby Rattle

The rattles do not comply with the size and shape requirements of the mandatory standard ‘Consumer Protection Notice No 14 of 2003- Consumer Product Safety Standard: Toys for children up to and including 36 months of age’.

MIC Gastrostomy Feeding Tubes - expanded recall

The Instructions For Use leaflet was not supplied with the product. The Instructions For Use provide important safety information for the user.

Trilogy Evo O2 and Trilogy Evo Portable Ventilators

Two software issues have been identified that relate to a pressure increase in the ventilators. 1. Infant/Pediatric External Flow Sensor (EFS) Calibration Pressure increase. An increase in the expiratory pressure (EPAP/PEEP) can occur when the paediatric/infant External Flow Sensor is used with an Active Flow or Dual Limb circuit and a manual circuit calibration is performed. 2. Pressure Drift (Continuous Usage). When a Trilogy Evo or Trilogy Evo O2 model is used continuously without any interruption to therapy, the baseline pressure may increase or decrease.

Expanded Recall: Various JHY Design Tabletop Firepots recalled due to lack of appropriate labelling and hazard information

LUCIRA CHECKIT COVID-19 TEST KIT (2021-10-08)

Alcohol Antiseptic 80% (v/v) Topical Solution Hand Sanitizer (2021-10-08)

Transseptal Needle Sets (2021-10-08)