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ResinAngel brand epoxy resin products recalled due to improper labelling

Apr 29, 2026Consumer product safety

ResinAngel brand epoxy resin products recalled due to improper labelling

Labelling and packaging

Custom made Zebra and Roller Blinds by SoHo Blinds recalled due to strangulation and choking hazards

Apr 27, 2026Consumer product safety

Custom made Zebra and Roller Blinds by SoHo Blinds recalled due to strangulation and choking hazards

Strangulation hazard - Choking hazard

Drugs and health products

H2O: Presence of particulate matter in affected lot

Health CanadaType II

H2O: Presence of particulate matter in affected lot

Contamination

Apr 24, 2026Drugs and health products

Fridababy Canadian model (water-filled) Not-Too-Cold-To-Hold Teethers recalled due to presence of microbe

Apr 24, 2026Consumer product safety

Fridababy Canadian model (water-filled) Not-Too-Cold-To-Hold Teethers recalled due to presence of microbe

Microbial hazard

Apr 23, 2026Medical devices

Vectorflow Antegrade Catheterization Product

Medical devices

Health CanadaType II

Vectorflow Antegrade Catheterization Product

Performance

CPSC

HappyGira Recalls Sweetie Baby and Style Life Eleven Baby Loungers Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products

Unknown Firm

CPSCGeneral Alert

HappyGira Recalls Sweetie Baby and Style Life Eleven Baby Loungers Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products

The baby loungers violate the mandatory standard for infant sleep products because the sides are shorter than the minimum side height limit to secure the infant and they do not have a stand, posing a fall hazard. Additionally, an infant can fall out of the enclosed opening at the foot of the lounger or become entrapped. Furthermore, the sleeping pad's thickness exceeds the maximum limit, posing a suffocation hazard. These violations create an unsafe sleeping environment for infants, posing a risk of serious injury or death.

Apr 23, 2026

CPSC

Autobrush Recalls Sonic Pro Children's Toothbrush Boxes Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries

Unknown Firm

CPSCGeneral Alert

Autobrush Recalls Sonic Pro Children's Toothbrush Boxes Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries

The recalled delivery boxes violate the mandatory standard for consumer products containing button cell and coin batteries because they contain a lithium coin battery that can be easily accessed by children, posing an ingestion hazard. The packaging also does not bear the required warning labels for products containing such batteries as required by Reese's Law. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

Apr 23, 2026

Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.

Apr 22, 2026Integra LifeSciences Corp. (NeuroSciences)

Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.

Increased rate of out-of-specification endotoxin results.

ALECENSARO (alectinib) and the Risk of Severe Hypertriglyceridemia

Marketed health products

Apr 22, 2026Marketed health products

ALECENSARO (alectinib) and the Risk of Severe Hypertriglyceridemia

New safety information - Product safety - Adverse reaction

Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.

Apr 22, 2026Integra LifeSciences Corp. (NeuroSciences)

Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.

Increased rate of out-of-specification endotoxin results.

LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

Linkbio Corp.

Apr 22, 2026Linkbio Corp.

LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.

The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.

Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.

Apr 22, 2026Integra LifeSciences Corp. (NeuroSciences)

Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.

Increased rate of out-of-specification endotoxin results.

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

Apr 22, 2026Integra LifeSciences Corp. (NeuroSciences)

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

Increased rate of out-of-specification endotoxin results.

THERAKOS DEVELOPMENT LIMITED

Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit Model/Catalog Number: CLXUSA Software Version: Not Applicable Product Description: THERAKOS Photopheresis or extracorporeal photopheresis (ECP) is a photoimmune therapy where leukocytes are separated from whole blood via apheresis, combined with a photoactive drug (8-methoxypsoralen) and then exposed to ultraviolet A (UVA) light. All blood components, including the treated leukocytes, are returned to the patient. THERAKOS¿ Photopheresis utilizes the THERAKOS CELLEX System to combine cell separation and photoactivation into a single, closed and sterile circuit. The THERAKOS CELLEX Photopheresis System collects the buffy coat (leukocyte-enriched blood) from the patient in a discontinuous flow process and intermittently returns the remaining plasma and erythrocytes to the patient. The buffy coat is passed through the photoactivation module where the drug is activated with a precise amount of UVA light determined by the characteristics of the individual patient s buffy coat. After photoactivation, the buffy coat is immediately returned to the patient s bloodstream. Component: Not Applicable

Apr 22, 2026THERAKOS DEVELOPMENT LIMITED

Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit Model/Catalog Number: CLXUSA Software Version: Not Applicable Product Description: THERAKOS Photopheresis or extracorporeal photopheresis (ECP) is a photoimmune therapy where leukocytes are separated from whole blood via apheresis, combined with a photoactive drug (8-methoxypsoralen) and then exposed to ultraviolet A (UVA) light. All blood components, including the treated leukocytes, are returned to the patient. THERAKOS¿ Photopheresis utilizes the THERAKOS CELLEX System to combine cell separation and photoactivation into a single, closed and sterile circuit. The THERAKOS CELLEX Photopheresis System collects the buffy coat (leukocyte-enriched blood) from the patient in a discontinuous flow process and intermittently returns the remaining plasma and erythrocytes to the patient. The buffy coat is passed through the photoactivation module where the drug is activated with a precise amount of UVA light determined by the characteristics of the individual patient s buffy coat. After photoactivation, the buffy coat is immediately returned to the patient s bloodstream. Component: Not Applicable

Increased difficulty in installing the centrifuge bowl onto the centrifuge bowl holder. Improper installation may cause the centrifuge bowl to dislodge, resulting in a broken bowl during the prime cycle or treatment phase, leading to a delay in patient treatment and blood loss.

Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL CERVICAL PLATE, ELEGANCE 4 LEVEL CERVICAL PLATE Model/Catalog Number: See Excel sheet attached named "FDA 5072 Product Information" Software Version: Not applicable Product Description: The Elegance¿Anterior Cervical plate is designed for use as a cervical plate system. It has a shape which restores the intervertebral height and lordosis. The Elegance¿ Anterior Cervical plate consists in a variety of shapes and sizes of cervical plates with rounded corners, featuring bone screw s holes, locking systems and bone screws. The plates go from one (1) to five (5) levels, and the screws are selfdrilling or self- tapping, and fixed or variable. The fixation is provided by the bone screws inserted into the vertebral body by means of an anterior approach. The Elegance¿plates, as well as the bone screws, are made of compliant ASTM F136 Titanium alloy. It is essential to insert the implants with the instrumentation specifically designed for this purpose. For more description of the instrumentation, read the technical documentation associated to the Elegance¿ Anterior Cervical plate. Detailed information concerning the surgical technique of the Elegance¿Anterior Cervical plate is available upon request, please contact CLARIANCE or its local representative.

Clariance-SAS

Apr 22, 2026Clariance-SAS

Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL CERVICAL PLATE, ELEGANCE 4 LEVEL CERVICAL PLATE Model/Catalog Number: See Excel sheet attached named "FDA 5072 Product Information" Software Version: Not applicable Product Description: The Elegance¿Anterior Cervical plate is designed for use as a cervical plate system. It has a shape which restores the intervertebral height and lordosis. The Elegance¿ Anterior Cervical plate consists in a variety of shapes and sizes of cervical plates with rounded corners, featuring bone screw s holes, locking systems and bone screws. The plates go from one (1) to five (5) levels, and the screws are selfdrilling or self- tapping, and fixed or variable. The fixation is provided by the bone screws inserted into the vertebral body by means of an anterior approach. The Elegance¿plates, as well as the bone screws, are made of compliant ASTM F136 Titanium alloy. It is essential to insert the implants with the instrumentation specifically designed for this purpose. For more description of the instrumentation, read the technical documentation associated to the Elegance¿ Anterior Cervical plate. Detailed information concerning the surgical technique of the Elegance¿Anterior Cervical plate is available upon request, please contact CLARIANCE or its local representative.

Due to a quality issue regarding the presence of burr on the finished cervical plate product.

Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.

Apr 22, 2026Integra LifeSciences Corp. (NeuroSciences)

Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.

Increased rate of out-of-specification endotoxin results.

Green Scenic Smoke and Carbon Monoxide Alarm recalled due to potential failure to operate

Apr 22, 2026Consumer product safety

Green Scenic Smoke and Carbon Monoxide Alarm recalled due to potential failure to operate

Unauthorized products

Pharmaceutical

Australia

Overseas-registered products available for cyclophosphamide and ifosfamide injection shortages

TGA

au-tgaMedicines Safet...

Overseas-registered products available for cyclophosphamide and ifosfamide injection shortages

Information about the cyclophosphamide and ifosfamide injection shortages....

Apr 21, 2026TGA

EcoSmart Fire Stix Portable Fire Pit and Mini T Designer Fireplace recalled due to fire hazard

Apr 21, 2026Consumer product safety

EcoSmart Fire Stix Portable Fire Pit and Mini T Designer Fireplace recalled due to fire hazard

Fire hazard

Various pistachios and pistachio-containing products made at Kunafa's recalled due to Salmonella

CFIA

Health CanadaClass 2

Various pistachios and pistachio-containing products made at Kunafa's recalled due to Salmonella

Salmonella

Apr 21, 2026CFIA

Expanded recall: Breez 2-in-1 Smart Bedroom Fan and White Noise Machine recalled due to fire hazard

Apr 21, 2026Consumer product safety

Expanded recall: Breez 2-in-1 Smart Bedroom Fan and White Noise Machine recalled due to fire hazard

Fire hazard