immediate action Recalls

2,679 recalls tagged with “immediate action”.

Health & Personal Care
HIGH
FDA DEVICE

C.R. Bard Recall: SureStep Foley Tray System Lubri-Sil I.C. Complete Care Contains Incorrect Inserts

C.R. Bard Inc. recalls 4,300 SureStep Foley Tray System Lubri-Sil I.C. Complete Care infection control Foley catheter trays nationwide in the United States. The trays may contain incorrect inserts that misrepresent material composition. The mismatch could trigger infections or allergic reactions. Health care providers should stop use and follow recall instructions immediately.

C.R. Bard
Foley catheter
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Health & Personal Care
HIGH
FDA DRUG

6,973 KleenFoam Antimicrobial Foam Soap Cartridges Recalled for Contamination Risk

DermaRite Industries recalled 6,973 cartridges of KleenFoam Antimicrobial Foam Soap on July 17, 2025. The products are contaminated with the bacteria Burkholderia cepacia, which poses significant health risks. Consumers must stop using the soap immediately and contact DermaRite for guidance.

KleenFoam
Microbial Contamination
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Health & Personal Care
HIGH
FDA DEVICE

CR Bard Recalls SureStep Foley Tray System A942216 for Incorrect Inserts (2025)

CR Bard recalled 3,670 SureStep Foley Tray System A942216 Foley Catheter Trays nationwide after discovering incorrect inserts. Mislabeling could cause infection or allergic reactions. Healthcare providers should stop using the device immediately and follow recall instructions from the manufacturer.

CR Bard
Foley catheter
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Health & Personal Care
HIGH
FDA DEVICE

Quest International Measles IgM 01-190M Recall for False Premarket Clearance

Quest International recalls 376 Measles IgM ELISA kits nationwide in Utah, Texas and Arizona after discovering the product lacks premarket approval or clearance. The high-risk health device carries a Class II designation. Stop using the device immediately and follow manufacturer recall instructions.

Quest International
Measles IgM
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Health & Personal Care
HIGH
FDA DRUG

PeriGiene Health Care Antiseptic Recalled for Burkholderia Contamination (2025)

Five thousand seven hundred three bottles recalled nationwide for microbial contamination with Burkholderia cepacia. DermaRite Industries LLC issued the recall on July 17, 2025. The product is PeriGiene Health Care Antiseptic, 222 mL bottles. Consumers should stop use and contact DermaRite for guidance.

PeriGiene
Microbial Contamination
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Health & Personal Care
HIGH
FDA DRUG

DermaSarra External Analgesic Recalled for Burkholderia Cepecia Contamination (DermaRite Industries)

DermaRite Industries recalled 249 bottles of DermaSarra External Analgesic on July 17, 2025 due to microbial contamination. The product, sold nationwide, carries NDC 61924-189-08 and Lot 40187.2 with an expiration date of February 2026. Consumers should stop using the product immediately and contact DermaRite for guidance.

DERMASARRA
Microbial Contamination
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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 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 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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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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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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Tag Statistics

Total Recalls
2,679

Related Tags

chemical hazardlaceration riskelectrical hazardinfant productadult productsuffocation riskstop use immediatelyreturn for refundfederal law violationcpsc regulatednhtsa regulatedrepair available