adult product Recalls

915 recalls tagged with “adult product”.

Health & Personal Care
HIGH
FDA DRUG

Taizhou Kangping Medical 3.85 Million Cartons of BZK Antiseptic Towelettes Recalled for Sterility LQ

Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes for external use. The U.S. FDA listing cites lack of assurance of sterility as the reason for recall. Consumers and healthcare providers should stop using this product immediately and contact the manufacturer for guidance.

Taizhou Kangping Medical Science And Technology Co.
Lack of
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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 DRUG

Ascend Laboratories Amlodipine and Olmesartan Medoxomil Recall for Low Dissolution 8,568 Bottles in

Ascend Laboratories recalls 8,568 bottles of Amlodipine and Olmesartan Medoxomil tablets due to failed dissolution specifications. The recall covers products manufactured by Alkem Laboratories in India and distributed nationwide in the USA. The defect involves low dissolution results. Stop use immediately and contact Ascend Laboratories for guidance.

Amlodipine and Olmesartan Medoxomil
Failed Dissolution
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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Cheese Recalled for Listeria Risk (2025)

Middlefield Original Cheese Cooperative recalled 640 pounds of cheese products due to potential Listeria monocytogenes contamination. The recall covers Monterey Jack and Farmers Cheese in multiple package sizes. Consumers should not eat the cheese and should contact the company for refunds or replacements.

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

Summa Therapeutics Recalls 22 Finesse BTK Multicath Angioplasty Balloons Over Burst Specifications (

Summa Therapeutics recalled 22 units of the Finesse BTK Multicath Injectable Angioplasty Balloon Catheter sold to healthcare facilities in New Jersey and Florida. The balloon may not meet burst specifications, raising risk during angioplasty. Healthcare providers must stop using the device immediately and follow recall instructions from Summa Therapeutics.

Finesse BTK Multicath
Potential for
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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 DEVICE

DJO Surgical ALTIVATE Glenoid Reamer Head Recall Expands to 927 Units

DJO Surgical recalled 927 ALTIVATE reverse wedge glenoid reamer heads distributed nationwide in the United States after concerns that the devices may kick or bind up during use. The issue involves model 804-06-311 and non-sterile stainless steel material. Healthcare providers and patients should stop using the device immediately and contact Encore Medical, LP for instructions.

DJO Surgical
Their is
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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 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

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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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 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 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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Tag Statistics

Total Recalls
915

Related Tags

fire hazardburn riskchemical hazardsuffocation riskinfant producttoddler productelderly productcpsc regulatedreturn for refundreplacement availableimmediate actionstop use immediately