adult product Recalls

989 recalls tagged with “adult product”.

Health & Personal Care
HIGH
FDA DEVICE

Ortho-Clinical Diagnostics LAC Slides Recalled Over Calibration Failures on VITROS Systems

VITROS Chemistry Products LAC Slides recalled after calibration failures on VITROS XT 3400 and VITROS XT 7600 systems. The recall covers catalog 8433880 with 2,908 units distributed nationwide in the US. Manufacturers warn that coating 0130 and above with Condition Code TH4-63J elevates calibration failures, delaying lac test results and potentially impacting patient management. Health providers,病

Ortho-Clinical Diagnostics
VITROS Chemistry
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Health & Personal Care
HIGH
FDA DRUG

Sucralfate Tablets Recall Expanded After CGMP Deviations; 26,992 Blister Packs Affected

A recall is active for Sucralfate Tablets, USP 1 gram distributed by American Health Packaging. The firm filed for Chapter 11 in September 2024, triggering CGMP deviations and questions about product identity, strength, quality and purity. The recall affects 26,992 blister packs distributed nationwide. Stop using the product and contact Amerisource Health Services or your clinician for guidance.

SUCRALFATE
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Ortoma AB Recalls 261 Inserter Adapters for Hip Cup Tools (2025)

Ortoma AB is recalling 261 Inserter Adapters for the Cup Inserter Tool used in hip replacement procedures sold worldwide, including Florida. The defect is weld breakage between the pin and the inserter holder. Surgeons and patients should stop using the devices immediately and follow the manufacturer's recall instructions.

Ortoma
Due to
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Health & Personal Care
HIGH
FDA DRUG

Quallent Duloxetine Delayed-Release Capsules 60 mg Recall Expanded for Impurity Above FDA Interim Lm

Quallent Pharmaceuticals Health LLC recalls 1,856 bottles of Duloxetine delayed-release capsules due to CGMP deviations and an impurity above FDA interim limits. The recall is active as of August 20, 2025. Patients and providers should stop use and contact Breckenridge Pharmaceutical or a healthcare provider for guidance.

DULOXETINE
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Zap Surgical Systems ZAP-X Radiosurgery System Recalled for 17 Units Worldwide in 2025

Zap Surgical Systems recalled 17 ZAP-X Radiosurgery System units worldwide, including US states FL, CO, NJ, NY and several countries. A software defect could cause the collimator to collide with patient shoulders or the patient table during long gantry moves after proximity errors. Clinicians and patients should stop using the device and follow recall instructions from the manufacturer.

Zap Surgical Systems
If the
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Health & Personal Care
HIGH
FDA DEVICE

Home Health US Recalled 4,661 One Step Sterile Lancets for Single Use (2025)

Home Health US recalled 4,661 One Step Sterile Lancets for Single Use sold nationwide through Amazon. The recall cites incorrect or missing Unique Device Identifier codes. Consumers should stop using the lancets immediately and follow the recall instructions from Home Health US or their healthcare provider.

Home Health US
Due to
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Health & Personal Care
HIGH
FDA DRUG

Cipla USA Albuterol Sulfate Inhalation Aerosol Recall Expanded for Stability Variance (2025)

Cipla USA Inc. recalls 20,352 packs of Albuterol Sulfate Inhalation Aerosol after failing stability specifications. The defective lots were distributed nationwide in the United States. The issue involves out of specification results in particle size distribution at the 12-month time point. Patients and healthcare providers should stop use and contact Cipla USA for guidance.

Cipla USA Inc.
Failed Stability
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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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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 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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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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Tag Statistics

Total Recalls
989

Related Tags

chemical hazardelectrical hazardfda regulatedcpsc regulatedimmediate actionstop use immediatelyreturn for refundreplacement availableinfant producttoddler productelderly productpet related