Every parent needs to see this: 353 high-risk children's product recalls currently active. Check your home now.

Parent Safety Alerts

386 baby and children's product recalls tracked. Protect your kids from dangerous toys, cribs, car seats, furniture, and other hazardous products.

386
Children's Recalls
353
High Risk Products
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Common Hazards to Children

  • Choking hazards: Small parts can detach from toys and baby products
  • Tip-over risk: Unstable furniture can crush children (deaths reported)
  • Suffocation: Unsafe sleep products, mattresses, and carriers
  • Chemical exposure: Lead paint, toxic materials in toys
  • Burn/fire hazards: Flammable children's clothing and products

Why Product Safety Matters for Parents

Every year, emergency rooms treat approximately 150,000 children under age 15 for toy-related injuries, according to the Consumer Product Safety Commission (CPSC). Many of these injuries could be prevented with better awareness of product recalls and safety standards.

Children are uniquely vulnerable to product hazards because they explore the world by touching, tasting, and testing everything around them. Products designed for adults may pose unexpected risks when children gain access to them, and even products specifically made for children can have manufacturing defects or design flaws.

Staying informed about recalls is one of the most effective ways to protect your children. When a recall is announced, the manufacturer has determined (or a government agency has found) that the product poses a genuine safety risk that warrants action.

Age-Specific Safety Concerns

Infants (0-12 months)

  • Sleep safety: Inclined sleepers, soft mattresses, and sleep positioners have caused deaths
  • Suffocation: Loose bedding, bumper pads, and soft surfaces in cribs
  • Formula recalls: Contamination and nutritional deficiencies

Toddlers (1-3 years)

  • Choking hazards: Small parts, magnets, and button batteries
  • Furniture tip-overs: Unsecured dressers, shelves, and TVs
  • Poisoning: Medications, cleaning products, lead paint

Children (4-12 years)

  • Sports equipment: Bicycle helmets, scooters, hoverboards
  • Electronics: Overheating devices and battery fires
  • Online purchases: Unregulated toys from third-party sellers

Before You Buy: Safety Checklist

  • Search RecallRadar for the product name and brand
  • Check age recommendations match your child
  • Look for JPMA certification on baby products
  • Verify the manufacturer is reputable
  • Inspect packaging for safety labels and certifications
  • Check for sharp edges, loose parts, or defects
  • Read reviews looking for safety concerns
  • Register the product with the manufacturer
Read the Complete Parent's Safety Guide
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Help other parents: Share this page with parent groups, playdate friends, and family members. Every parent deserves to know about these safety alerts.

Showing 24 of 386 children's product recalls
353 high-risk products
Health & Personal Care
HIGH
FDA DRUG

Sun Pharmaceutical Radiopharmaceutical Kit Recall: 1,870 Kits Recalled for OOS Dissolution Issue

Sun Pharmaceutical Industries recalled 1,870 kits nationwide after an out-of-specification dissolution test for sulphate in Sodium Tartrate Dihydrate used to produce Mertiatide. The recall affects Rx-only kits distributed across the U.S. Healthcare providers and patients should stop using the product immediately and follow guidance from Sun Pharmaceutical. Contact information is provided by the UQ

Sun Pharmaceutical Industries
Failed Dissolution
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Food & Beverages
HIGH
FDA FOOD

New Spirit Naturals Ultra Whey Protein Powder Recalled for Undeclared Milk Allergen

New Spirit Naturals recalled 37 units of Ultra Whey Protein Powder sold directly through its online store after undeclared milk allergen was detected. The recall is currently active with a high-hazard designation. Consumers who have purchased the product should not consume it and should contact the company for refunds or replacements.

New Spirit Naturals
undeclared allergen
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Recalls 8,368 CLEARLINK CONTINU-FLO IV Sets for Leakage Risk (2025)

Baxter Healthcare recalled 8,368 CLEARLINK SYSTEM CONTINU-FLO IV sets nationwide after reports the devices may leak. The non-vented sets include a 0.2-micron filter, three CLEARLINK luer activated valves and a backcheck valve, and measure 102 inches in length. Hospitals and clinicians should stop using these units immediately and follow Baxter's recall instructions.

Baxter Healthcare
IV sets
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Recalled Lulive 12-Drawer Dresser (front)
HIGH
CPSC

Lulive 12-Drawer Dressers Recalled for Tip-Over Risk in 2025

Lulive recalled 12-drawer dressers sold on Amazon after identifying a risk of serious injury or death from tip-over and entrapment. The dressers are white with a metal frame, a wooden top, 12 collapsing fabric drawers, four side pockets and two hooks. They measure about 12 inches by 39 inches by 45 inches and weigh 30 pounds. Consumers should stop using unanchored dressers immediately and contactL

Lulive
The recalled
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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Recalls 7,455 lbs Shredded Mozzarella/Provolone (5-lb Bags)

Middlefield Original Cheese Cooperative recalled 364.125 cases of shredded Mozzarella/Provolone cheese sold in Ohio, Pennsylvania, Wisconsin, and Texas. The recall is due to potential contamination with Listeria monocytogenes. Consumers who purchased this product should not consume it and should contact the cooperative for refund or replacement information.

Middlefield Original Cheese Cooperative
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Pepper Jack Cheese Recalled Over Listeria Risk in 364 Cases

Middlefield Original Cheese Cooperative Pepper Jack Cheese is recalled across Ohio, Pennsylvania, Wisconsin and Texas. The recall covers 364.125 cases, about 7,455 pounds, due to potential contamination with Listeria monocytogenes. Consumers should not consume the product and should contact Middlefield Original Cheese Cooperative for refund or replacement information.

Middlefield Original Cheese Cooperative
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Middlefield Organic Gouda Cheese Recall: 364 Cases Over Listeria Contamination (2025)

Middlefield Original Cheese Cooperative is recalling 364 cases of Organic Gouda Cheese, 8 oz, packaged 12 per case and distributed in Ohio, Pennsylvania, Wisconsin and Texas, after potential contamination with Listeria monocytogenes. The product poses a high risk of serious illness if consumed. Consumers should not eat the cheese and should contact the cooperative for a refund or replacement.

Middlefield Original Cheese Cooperative
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Recalls 364 Cases of Cheddar Cheese Over Listeria (2025)

Middlefield Original Cheese Cooperative recalled 364.125 cases (7,455 pounds) of All Natural Mild Cheddar Cheese and Shredded Cheddar Cheese sold at retailers in Ohio, Pennsylvania, Wisconsin and Texas. Listeria monocytogenes contamination is the stated hazard. Consumers should not consume the cheese and should contact the cooperative for a refund or replacement.

Middlefield Original Cheese Cooperative
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Country Eggs Shell Egg Recall Affects 81,542 Dozen Across CA and NV

Country Eggs LLC recalled 81,542 dozen shell eggs distributed to 11 consignees in California and Nevada due to potential salmonella contamination. The recall covers Nagatoshi, Nijiya, Mizuho, and Sunshine yolk varieties sold in large AA Brown egg cartons. Consumers should not eat these eggs and should seek refund or replacement.

Country Eggs
Shell egg
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Pacemakers Recalled in Class I High-Hazard Software Issue Affecting ACCOLADE, VERS

Boston Scientific recalled 7,488 pacemakers worldwide due to software that could impair Safety Mode initiation in high-battery-impedance states. Devices include ACCOLADE family models and CRT-Ps such as VISIONIST and VALITUDE. The issue stems from software designed to enhance Safety Architecture. Patients should follow manufacturer instructions and contact providers immediately.

Boston Scientific
Software to
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Pacemakers Recalled for Safety-Mode Initiation Software Flaw (2025)

Boston Scientific recalled 1,050 pacemaker units worldwide on Aug 20, 2025. The recall covers ACCOLADE family devices and Visionist and Valitude CRT-Ps. A software issue could prevent Safety Mode initiation in ambulatory settings. Patients should follow manufacturer guidance and contact their clinician immediately.

Boston Scientific
Software to
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Pacemakers Recalled Over Software Flaw in Safety Architecture (2025)

Boston Scientific recalls 223,163 pacemakers worldwide due to software issues affecting Safety Architecture. The recall covers ACCOLADE, PROPONENT, ESSENTIO, ALTRUA 2 DR devices and VISIONIST and VALITUDE CRT-Ps. The defect prevents initiation of Safety Mode when battery impedance is high. Patients should stop using the device and follow manufacturer instructions.

Boston Scientific
Software to
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Pacemakers Recalled for Software Flaw That Could Block Safety Mode

Boston Scientific recalled 32,695 ACCOLADE family pacemakers and related CRT-Ps after discovering software that could prevent entering Safety Mode when battery impedance is high. The recall is worldwide and classified as Class I with a high hazard level. Patients should stop using the devices and follow manufacturer instructions. Contact Boston Scientific or a healthcare provider for guidance.

Boston Scientific
Software to
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Pacemakers Recalled in 2025 for Safety Architecture Software Flaw

Boston Scientific recalled 34,180 devices worldwide on 2025-08-20 for ACCOLADE family pacemakers and CRT-Ps due to software that could prevent Safety Mode in high battery impedance conditions. The defect affects ACCOLADE, PROPONENT, ESSENTIO, ALTRUA 2 DR SL and EL models, plus VISIONIST and VALITUDE CRT-P devices. Patients should stop using the devices and follow recall instructions.

Boston Scientific
Software to
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Pacemakers Recalled for High Battery Impedance Safety Software

Boston Scientific recall affects 4,055 pacemakers worldwide. The recall covers ACCOLADE family devices, ALTRUA 2 DR SL/EL, VISIONIST and VALITUDE CRT-P models. Software intended to enhance Safety Architecture can fail to initiate Safety Mode in ambulatory settings. Patients should stop using the device and contact their clinician.

Boston Scientific
Software to
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Health & Personal Care
HIGH
FDA DRUG

B. Braun Lactated Ringers Injection 46,032 Containers Recalled Over Particulate Matter

B. Braun Medical recalled 46,032 containers of Lactated Ringers Injection USP sold nationwide in the United States. The recall cites the presence of particulate matter in the 1000 mL IV solution. Consumers should stop using the product immediately and contact their healthcare provider or B. Braun for guidance.

B Braun Medical
Presence of
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Food & Beverages
HIGH
FDA FOOD

ADMIRAL OF THE FLEET, PORTICO SEAFOOD CLASSIC Breaded Shrimp Recalled Over Cs-137 Contamination (120

ADMIRAL OF THE FLEET and PORTICO SEAFOOD CLASSIC Cleantail Breaded Butterfly Shrimp is recalled by TAMPA MAID FOODS, LLC after the FDA identified Cesium-137 contamination. The recall covers 1,200 cases distributed to multiple states. Consumers should not consume the product and should contact TAMPA MAID FOODS for refund or replacement.

ADMIRAL OF THE FLEET
Product may
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Recalled STWUQIKONG Spiral Tower Toy
HIGH
CPSC

STWUQIKONG Three-Tier Spiral Tower Toy Recalled for Choking Hazard (2025)

STWUQIKONG recalled a three-tier spiral tower toy sold on Shein because of a choking hazard. The recall was announced on August 14, 2025. The toy includes three yellow balls and is designed for children under three, violating the small-ball ban. Stop using the product immediately and email STWUQIKONG_RECALL@hotmail.com to receive a full refund.

STWUQIKONG
The recalled
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Food & Beverages
HIGH
FDA FOOD

Fresh & Ready Foods Tuscan Artichoke and Mozzarella Salad Recalled for Undeclared Allergens (8.5 oz)

Fresh & Ready Foods recalled 233 units of Tuscan Artichoke and Mozzarella Salad distributed to 15 California locations after undeclared wheat and milk allergens were found. The allergen was not declared on the label. Consumers should not eat the product and should contact Fresh & Ready Foods LLC for refunds or replacements via email.

Fresh & Ready Foods
undeclared allergen
Read more
Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter UniCel DxH 800 Hematology Analyzers Recalled for High Hemoglobin Readings in High-WB

Beckman Coulter recalled the UniCel DxH 800 COULTER Cellular Analysis System configured with the Led HGB photometer. The recall affects models B24802, 629029, and B63322 and related configurations. A design-linked issue can yield erroneously high hemoglobin results when samples have elevated white blood cell counts. Stop using the device and follow the manufacturer’s recall instructions. Contact a

Beckman Coulter
Hematology analyzers
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