Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,116 results
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026130 - INTERNATIONAL MOTORS

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026130 - INTERNATIONAL MOTORS

Structure

Apr 2, 2026TC
Safety AlertUSCPSC

Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates the Small Ball Ban; Sold on Amazon by Beestech

Unknown Firm
Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates the Small Ball Ban; Sold on Amazon by Beestech
CPSCGeneral Alert

Children's Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violates the Small Ball Ban; Sold on Amazon by Beestech

The recalled spiral tower toy sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.

Apr 2, 2026
Safety AlertUSCPSC

ELENKER Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Fuzhou Shiahaha Cultural Industry Development

Unknown Firm
ELENKER Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Fuzhou Shiahaha Cultural Industry Development
CPSCGeneral Alert

ELENKER Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Fuzhou Shiahaha Cultural Industry Development

The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.

Apr 2, 2026
Safety AlertUSCPSC

Samson International Recalls Bellevue and Oaklynn Canopy Bed Frames Due to Impact and Injury Hazards

Samson International, of High Point, North Carolina
Samson International Recalls Bellevue and Oaklynn Canopy Bed Frames Due to Impact and Injury Hazards
CPSCGeneral Alert

Samson International Recalls Bellevue and Oaklynn Canopy Bed Frames Due to Impact and Injury Hazards

The canopy beams of the bed frames can collapse primarily when the bed is moved, posing impact and injury hazards to consumers.

Apr 2, 2026Samson International, of High Point, North Carolina
Safety AlertUSCPSC

E Mishan Recalls Granitestone Diamond Pro Blue Stainless Sauté Pans Due to Impact and Burn Hazards

Unknown Firm
E Mishan Recalls Granitestone Diamond Pro Blue Stainless Sauté Pans Due to Impact and Burn Hazards
CPSCGeneral Alert

E Mishan Recalls Granitestone Diamond Pro Blue Stainless Sauté Pans Due to Impact and Burn Hazards

The metal cap on the screw that connects the sauté pan to the handle can become detached and forcefully eject when heated, posing impact and burn hazards to consumers.

Apr 2, 2026
Vehicle RecallUSNHTSA

Keystone RV Company - Underbelly May Detach During Transit

Keystone RV Company
NHTSASTRUCTURE

Keystone RV Company - Underbelly May Detach During Transit

A detached underbelly can become a road hazard for other vehicles, increasing the risk of a crash.

Apr 2, 2026Keystone RV Company
Safety AlertUSCPSC

Sam's Club Recalls Member's Mark Children's Pajama Sets Due to Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear

Hansoll Textile Ltd., of South Korea
Sam's Club Recalls Member's Mark Children's Pajama Sets Due to Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
CPSCGeneral Alert

Sam's Club Recalls Member's Mark Children's Pajama Sets Due to Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear

The recalled pajama sets violate the mandatory standards for flammability of children's sleepwear, posing a risk of burn injuries to children.

Apr 2, 2026Hansoll Textile Ltd., of South Korea
Safety AlertUSCPSC

Coluans Christmas Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by BUDI Official

Unknown Firm
Coluans Christmas Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by BUDI Official
CPSCGeneral Alert

Coluans Christmas Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by BUDI Official

The recalled light-up rings violate the mandatory safety standard for toys because the battery compartment within the LED light ring contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

Apr 2, 2026
Safety AlertUSCPSC

OCUN NA Recalls Condor HMS Triple Carabiners Due to Risk of Serious Injury or Death from Fall Hazard

Unknown Firm
OCUN NA Recalls Condor HMS Triple Carabiners Due to Risk of Serious Injury or Death from Fall Hazard
CPSCGeneral Alert

OCUN NA Recalls Condor HMS Triple Carabiners Due to Risk of Serious Injury or Death from Fall Hazard

The carabiner's gate can malfunction where the gate does not close automatically and has to be closed manually by hand, posing a risk of serious injury or death due to falling.

Apr 2, 2026
Safety AlertUSCPSC

Tuymec Minoxidil Hair Growth Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by DrHealBeauty

Unknown Firm
Tuymec Minoxidil Hair Growth Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by DrHealBeauty
CPSCGeneral Alert

Tuymec Minoxidil Hair Growth Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by DrHealBeauty

The hair serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.

Apr 2, 2026
Food & BeverageFranceRappelConso

sans marque - coque élevée en france

sans marque
RappelConsovolontaire (san...

sans marque - coque élevée en france

non conformite microbiologique

Apr 2, 2026sans marque
Food & BeverageFranceRappelConso

donna indiana professional - donna indiana professional gluhen hair cuticle restore mask

donna indiana professional
RappelConsovolontaire (san...

donna indiana professional - donna indiana professional gluhen hair cuticle restore mask

présence d’un mélange de methylchloroisothiazolinone et de methylisothiazolinone (annexe v, n°39) ¤

Apr 2, 2026donna indiana professional
Vehicle RecallUSNHTSA

BMW of North America, LLC - Reverse Gear Control Unit May Overheat

BMW of North America, LLC
NHTSAPOWER TRAIN

BMW of North America, LLC - Reverse Gear Control Unit May Overheat

An overheated reverse gear control unit increases the risk of a fire.

Apr 2, 2026BMW of North America, LLC
Medical DeviceUSFDA Devices

Philips X7-2 Ultrasound Transducer

Philips Ultrasound, Inc
FDA DevicesClass III

Philips X7-2 Ultrasound Transducer

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

Apr 1, 2026Philips Ultrasound, Inc
Medical DeviceUSFDA Devices

Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use

Erbe USA Inc
FDA DevicesClass I

Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use

Probes may rupture/burst during activation

Apr 1, 2026Erbe USA Inc
Medical DeviceUSFDA Devices

Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP DRESSING,COLLAGEN,PURACOL PLUS, 2X2.2"

Medline Industries, LP
FDA DevicesClass II

Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP DRESSING,COLLAGEN,PURACOL PLUS, 2X2.2"

Elevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation, delayed wound healing, or systemic effects such as fever and hypotension. In severe cases, septic shock may result.

Apr 1, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

Brand Name: Olympus HALO PKS Cutting Forceps, 5mm 33cm Product Name: HALO PKS Cutting Forceps Model/Catalog Number: HACF0533 Product Description: The HALO PKS Cutting Forceps are intended to be passed through a 5 mm laparoscopic cannula. Coagulation is achieved using electrosurgical energy under laparoscopic visualization. The device is intended to be used with the Gyrus ACMI G400 Workstation only.

Olympus Corporation of the Americas
FDA DevicesClass II

Brand Name: Olympus HALO PKS Cutting Forceps, 5mm 33cm Product Name: HALO PKS Cutting Forceps Model/Catalog Number: HACF0533 Product Description: The HALO PKS Cutting Forceps are intended to be passed through a 5 mm laparoscopic cannula. Coagulation is achieved using electrosurgical energy under laparoscopic visualization. The device is intended to be used with the Gyrus ACMI G400 Workstation only.

Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.

Apr 1, 2026Olympus Corporation of the Americas
Medical DeviceUSFDA Devices

Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers: 21031-3, 21031-5, 21032-11, 21032-3, 21032-5, 21033-3, 21033-5, 21034-3, 21034-5, 21035-3, 21036-3.

I.T.S. GmbH
FDA DevicesClass II

Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers: 21031-3, 21031-5, 21032-11, 21032-3, 21032-5, 21033-3, 21033-5, 21034-3, 21034-5, 21035-3, 21036-3.

Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

Apr 1, 2026I.T.S. GmbH
Medical DeviceUSFDA Devices

Philips OMNI III TEE Ultrasound Transducer

Philips Ultrasound, Inc
FDA DevicesClass III

Philips OMNI III TEE Ultrasound Transducer

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

Apr 1, 2026Philips Ultrasound, Inc
Food & BeverageFranceRappelConso

donna indiana / queen care - gluhen hair cuticle restore mask / gloss volume reducer liso espelhado

donna indiana / queen care
RappelConsovolontaire (san...

donna indiana / queen care - gluhen hair cuticle restore mask / gloss volume reducer liso espelhado

présence d’une substance interdite : formaldéhyde (cancérogène/mutagène)

Apr 1, 2026donna indiana / queen care
Vehicle RecallUSNHTSA

Mack Trucks, Inc. - Turn Signal Failure/FMVSS 108

Mack Trucks, Inc.
NHTSAEXTERIOR LIGHTING

Mack Trucks, Inc. - Turn Signal Failure/FMVSS 108

Turn signals that do not function properly may fail to indicate the driver's intention to change vehicle direction, increasing the risk of a crash.

Apr 1, 2026Mack Trucks, Inc.
Medical DeviceUSFDA Devices

ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-NE5/C, DC21454035/C, DC21455550/C

Merit Medical Systems, Inc.
FDA DevicesClass I

ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-NE5/C, DC21454035/C, DC21455550/C

16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.

Apr 1, 2026Merit Medical Systems, Inc.
PharmaceuticalUSFDA Drugs

Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Princeton, NJ, Manufactured by: Macleods Pharmaceuticals Ltd., Sarigam, Valsad, Guajarat, INDIA NDC 33342-401-44

MACLEODS PHARMA USA, INC
FDA DrugsClass II

Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Princeton, NJ, Manufactured by: Macleods Pharmaceuticals Ltd., Sarigam, Valsad, Guajarat, INDIA NDC 33342-401-44

Subpotent Drug

Apr 1, 2026MACLEODS PHARMA USA, INC
Medical DeviceUSFDA Devices

Brand Name: Olympus PKS Cutting Forceps w/Cord, 5mm 24cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920000PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the PKS electrical generator.

Olympus Corporation of the Americas
FDA DevicesClass II

Brand Name: Olympus PKS Cutting Forceps w/Cord, 5mm 24cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920000PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the PKS electrical generator.

Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.

Apr 1, 2026Olympus Corporation of the Americas

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