Recalls published in July 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in July 2026, newest first.
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Highest risk · 3 months ago
Target Cat & Jack Children's Sandals recall: Risk of Serious Injury or Death from Choking Hazard
Risk of Serious Injury or Death from Choking Hazard
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Highest risk · 3 months ago
SDADI Kitchen Step Stools, models LT01 and LT05 recall: The recalled tower stools can collapse or tip over while in use
The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing…
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Highest risk · 3 months ago
Panasonic Electric Toaster Ovens recall: Shock and Fire Hazards
Shock and Fire Hazards
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Highest risk · 3 months ago
Oitnlaughter LED Finger Lights recall: The recalled finger lights violate the mandatory safety standard for toys
The recalled finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by…
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Highest risk · 3 months ago
Noerishia Adult Portable Bed Rails recall: The recalled bed rails violate the mandatory standard for adult portable bed
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between…
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Highest risk · 3 months ago
Mnient Adult Portable Bed Rails recall: The recalled bed rails violate the mandatory standard for adult portable bed
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between…
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Highest risk · 3 months ago
Madewell Women's Sweaters recall: Due to Risk of Serious Injury or Death from Burn Hazard
Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Clothing Textiles
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Highest risk · 3 months ago
Liizousuda recall: The paint thinner contains low-viscosity petroleum distillates
The paint thinner contains low-viscosity petroleum distillates, which must be in child-resistant packaging, as required by the Poison Prevention…
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Highest risk · 3 months ago
Jobon butane torch lighters recall: The lighters violate the mandatory safety standard for multipurpose lighters
The lighters violate the mandatory safety standard for multipurpose lighters because they do not have the required child-resistant mechanisms posing…
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Highest risk · 3 months ago
Huish Outdoors Hollis Diving Regulators recall: Risk of Serious Injury or Death from Drowning
Risk of Serious Injury or Death from Drowning
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Highest risk · 3 months ago
Currey & Company Nottaway Chandeliers recall: Risk of Serious Injury or Death from Electrocution Hazard
Risk of Serious Injury or Death from Electrocution Hazard
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NHTSA safety recall · 3 months ago
Nissan Armada, Infiniti QX56 and and 2014-2027 QX80 recall: The Gross Axle Weight Rating (GAWR) listed on the certification label
The Gross Axle Weight Rating (GAWR) listed on the certification label is incorrect, which can allow the vehicle to be overloaded. As such, these…
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Class II · 3 months ago
Integra LifeSciences Corp. OmniTract Surgical Retractor System recall: The current Omni-Tract Surgical Retractor System IFU states a dry time of 30
The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to…
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Class II · 3 months ago
Medline recall: Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots…
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Class II · 3 months ago
Encore Medical, LP Brand Name: Empowr 3D Knee Product Name: Empowr 3D Knee INS recall: Due to packaging discrepancy with incorrect product size mixed
Due to packaging discrepancy with incorrect product size mixed up.
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Class II · 3 months ago
Encore Medical, LP Brand Name: Empowr 3D Knee Product Name: Empowr 3D Knee INS recall: Due to packaging discrepancy with incorrect product size mixed
Due to packaging discrepancy with incorrect product size mixed up.
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Class II · 3 months ago
Medline recall: Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots…
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Class II · 3 months ago
Boston Scientific Neuromodulation Corporation Intracept Access Instruments recall: Intraosseous nerve ablation system instruments may have sterile barrier
Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility…
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Class II · 3 months ago
Biomerieux Inc Vitek 2 Ast-N447 Test KIT Product reference 424620 recall: Potential for false resistant carbapenem and/or cephalosporin results
Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil…
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Class II · 3 months ago
Think Surgical, Inc. Tmini Femur Tracking Array REF 109003 Udi-Di code: M9461090030 recall: Due to manufacturing/design issue where the knob on the tracking array
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
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Class II · 3 months ago
Elekta, Inc. Brand Name: Geneva Product Name: Brachytherapy Applicator recall: Due to safety concerns regarding the detachment of the tip
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
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Class II · 3 months ago
Elekta, Inc. Brand Name: Brachytherapy Applicator Product Name: Advanced recall: Due to safety concerns regarding the detachment of the tip
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
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Class II · 3 months ago
Fresenius Medical Care Holdings, Inc. 5008X Blood Tubing Set recall: Potential for Online Port Errors due to connection issues when connecting
Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the…
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Class II · 3 months ago
Elekta, Inc. Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name recall: Due to safety concerns regarding the detachment of the tip
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.