suffocation risk Recalls

495 recalls tagged with “suffocation risk”.

Example of child using the compression strap to stand on above-ground pool, illustrating the hazard involved
CRITICAL
CPSC

Bestway, Intex and Polygroup Recall 48-Inch+ Above-Ground Pools Over Drowning Hazard (2025)

Bestway, Intex and Polygroup recall 5 million above-ground pools taller than 48 inches after nine deaths. The recall covers pools whose model numbers are printed on the liner outside the pool. The hazard stems from a compression strap around the pool legs that can create a foothold for a child, enabling access to the water. Stop using the pools immediately and contact the respective brands for a维修

Bestway
The compression
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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Pepper Jack Cheese Recalled for Listeria Contamination (2025

Middlefield Original Cheese Cooperative recalled Pepper Jack cheese products sold in Kentucky, Ohio and Pennsylvania after diet contamination concerns. The recall covers 8 oz. individual units, 5 lb loaves and 40 lb loaves with lot code 251661. The hazard is possible contamination with Listeria monocytogenes. Consumers should not eat the product and should contact the company for refund or a safe-

Middlefield Original Cheese Cooperative
Potential contamination
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Health & Personal Care
HIGH
FDA DEVICE

DJO Surgical Recalls 447 ALTIVATE Reverse Glenoid Reamer Sleeve Units (2025)

DJO Surgical is recalling 447 ALTIVATE Reverse Glenoid Reamer Sleeve devices distributed nationwide in the United States. The device may kick or bind up during or immediately prior to use. Healthcare providers and patients should stop using the device and follow recall instructions issued by Encore Medical, LP via email.

DJO Surgical
Their is
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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 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 DEVICE

Stryker Communications Recalls 40 Medical Light Systems Over Powder Coating Chip Risk (2025)

Stryker Communications recalls 40 surgical light systems nationwide after reports of stress lines in the powder coating. The devices include CH00000001 and the SLX to Oculan NFC Upgrade Kit, P60034. The recall is active as of July 15, 2025. Patients and healthcare providers should stop using the devices immediately and follow manufacturer recall instructions.

Stryker Communications
Surgical lights
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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 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 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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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

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 DEVICE

North American Rescue JETT Medical Device Recall for Lower-Limb Occlusion Tool (2025)

North American Rescue recalled 552 units of the JETT device, used for occlusion of blood flow to the lower limbs, due to a manufacturing defect that may compromise structural integrity and performance. The recall covers multiple kits distributed worldwide, including U.S. states and several international countries. Stop using the device immediately and await recall instructions from the company or

North American Rescue
Device used
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Deep Sprouted Mat 16 oz Recalled for Salmonella Risk 2025

CHETAK NEW YORK LLC recalled 5,232 packets of Deep Sprouted Mat 16 oz distributed to California, New Jersey, Illinois, Florida and Texas after tests found Salmonella. The recall class is I with a high hazard level. Consumers should not consume the product and should seek refund or replacement by email.

CHETAK NEW YORK
Product tested
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Tag Statistics

Total Recalls
495

Related Tags

infant productchildren productoutdoormetalplasticimmediate actionstop use immediatelyrepair availablereplacement availablereturn for refundholiday productsummer product