All Product Recalls

Browse through 3,495 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Recalled Dearlomum retractable safety gate-black
HIGH
CPSC

Dearlomum Retractable Safety Gate Recall 2025 for Entrapment Hazard (SH20.006D)

Dearlomum retractable mesh safety gates sold on Amazon by Signbaby are recalled. The gates violate federal expansion gate standards because a child's torso can fit through the base opening, creating a risk of serious injury or death from entrapment. Stop using the recalled gates immediately and contact Signbaby for a full refund; disassemble, destroy the mesh, and email a photo to regcards.team@gm

Dearlomum
The recalled
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Recalled Ozark Trail 64 oz Stainless-Steel Insulated Water Bottle, model 83-662
MEDIUM
CPSC

Walmart Recalls Ozark Trail 64 oz Water Bottles for Lid Ejection Hazard (2025)

Walmart recalls Ozark Trail 64 oz stainless steel insulated water bottles sold at Walmart due to a lid ejection hazard. The one-piece screwcap lid can forcefully eject when opened after liquids are stored inside, creating a risk of impact and laceration. Stop using the recalled bottles and contact Walmart for a full refund.

Walmart
The lid
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Recalled SPPTTY Kids 14-inch Bicycle in Pink
HIGH
CPSC

SPPTTY Kids Bicycles Recalled for Lead Poisoning Risk (2025)

SPPTTY recalled kids bicycles sold at Walmart after lead levels exceeded the federal lead content ban in multiple components and on the black paint used on pumps. The recall urges consumers to stop using the bicycles immediately. To receive a refund, dismantle the bicycles, photograph the setup, and email the photo to lishkjie@163.com; after destruction is verified, dispose of the bike.

SPPTTY
Multiple components
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Health & Personal Care
HIGH
FDA DEVICE

BioFire Defense FilmArray NGDS Warrior Panel NGDS-ASY-0007 Recall 130 Kits in 2025

BioFire Defense recalled 130 FilmArray NGDS Warrior Panel NGDS-ASY-0007 kits distributed nationwide in the United States. The recall cites an increased risk of internal control failures when testing positive blood cultures. Clinicians should stop using the device immediately and follow recall instructions provided by BioFire Defense. Notification is by letter to affected facilities.

BioFire Defense
FilmArray NGDS
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Recalled Creekliybear "Pack and Play" Aftermarket Play Yard Mattress
MEDIUM
CPSC

Creekliybear Play Yard Mattress Recalled Over Entrapment Risk (2025)

Creekliybear recalled its Pack and Play aftermarket mattresses sold on Amazon by Kbabyea on July 10, 2025. The mattresses exceed thickness standards and may not fit certain play yards, creating a suffocation entrapment risk. Parents should stop using the mattresses immediately and contact Kbabyea for a full refund.

Creekliybear
The aftermarket
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Recalled WLIVE Fabric 15-Drawer Dresser in Rustic Brown
HIGH
CPSC

WLIVE Fabric 15-Drawer Dressers Recalled for Tip-Over Risk Sold on Amazon (2025)

WLIVE recalled its Fabric 15-Drawer Dressers sold on Amazon after reports of tip-over and entrapment hazards. The dressers can tip when not anchored to a wall, posing serious injury or death risk to children and violating the STURDY standard. Consumers should stop using unanchored dressers and contact WLIVE for a full refund.

WLIVE
The recalled
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Health & Personal Care
HIGH
FDA DRUG

Boothwyn Pharmacy Semaglutide Injection Recall for Subpotent Drug (High-Risk)

Boothwyn Pharmacy LLC issued a nationwide recall of 186 vials of Semaglutide 2.5 mg/mL injection, 0.8 mL, on July 9, 2025. The FDA enforcement report classifies the recall as Class II with a high hazard level. Consumers and healthcare providers should stop using the product immediately and follow guidance from Boothwyn Pharmacy or a healthcare provider.

Boothwyn Pharmacy
Subpotent Drug
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Health & Personal Care
HIGH
FDA DRUG

Boothwyn Pharmacy Semaglutide Injection Recall for Subpotent Drug (4 mL, 2.5 mg/mL)

Boothwyn Pharmacy recalls 648 vials of semaglutide 2.5 mg/mL injection nationwide after detecting subpotent potency. The recall involves products distributed across the U.S. and is classified as Class II with a high hazard level. Stop using the product and contact Boothwyn Pharmacy or a healthcare provider for guidance.

Boothwyn Pharmacy
Subpotent Drug
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Health & Personal Care
HIGH
FDA DRUG

H-E-B inControl Alcohol Pads Recalled for Subpotent Isopropyl Alcohol (2025)

H-E-B and its inControl brand recall 300,000 sterile alcohol pads nationwide after the FDA alerted a subpotent isopropyl alcohol concentration. The pads were packaged in China with components from Taiwan and distributed nationwide. Consumers should stop using the product immediately and seek guidance from healthcare providers or MEDLINE INDUSTRIES, LP.

H-E-B
Subpotent Drug-
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Health & Personal Care
HIGH
FDA DRUG

CURAD Alcohol Prep Pads Recall for Subpotent Isopropyl Alcohol (2025)

CURAD Alcohol Prep Pads recalled nationwide after tests found isopropyl alcohol levels subpotent. Medline Industries is the maker listed on recall documents. The issue concerns diluted potency below labeled concentration. Stop using immediately and contact Medline for guidance.

CURAD
Subpotent Drug-
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Health & Personal Care
HIGH
FDA DRUG

Medline Alcohol Prep Pads Recalled for Subpotent Isopropyl Alcohol in 6669874 Units

Medline Industries recalled 6,669,874 units of Alcohol Prep Pads nationwide after detecting subpotent isopropyl alcohol. The pads were distributed nationwide. The recall is classified as Class II with a high hazard level. Consumers and healthcare providers should stop using the product immediately and contact Medline for guidance.

Medline Alcohol Prep
Subpotent Drug-
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Health & Personal Care
HIGH
FDA DRUG

Rite Aid Alcohol Prep Pads Recalled Over Subpotent Isopropyl Alcohol Levels (2025)

Rite Aid alcohol prep pads distributed nationwide are recalled after subpotent isopropyl alcohol levels were found below label concentration. Medline Industries, LP notified distributors and healthcare providers in a Class II recall dated July 7, 2025. Consumers and healthcare providers should stop using the product immediately and seek guidance from a healthcare provider.

Rite Aid
Subpotent Drug-
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Food & Beverages
HIGH
FDA FOOD

Evergreen Orchard Farm Grape Juice Recalled in 78 Cases for 2025 Pasteurization Lapse

Evergreen Orchard Farm recalled 78 cases of Grape Juice in 4 oz foil pouches distributed to PA, NJ and NY. The recall cites lack of pasteurization and sanitation records. Consumers who purchased the product should not consume it and should contact Evergreen Orchard Farm, LLC via Email for refund or replacement.

Evergreen Orchard Farm
Lack of
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