adult product Recalls

915 recalls tagged with “adult product”.

Health & Personal Care
HIGH
FDA DEVICE

Cardinal Health 200 Salem Sump Anti-Reflux Valve Recalled for Breakage Risk (2025)

Cardinal Health 200, LLC recalls all lots of the Salem Sump Anti-Reflux Valve worldwide after complaints of valve breakage. The recall covers CE-marked valves with multiple identifiers. Hospitals and clinicians should stop using the device immediately and follow manufacturer instructions. This notice alerts providers to check for the affected code and act now.

Cardinal Health
Firm has
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Health & Personal Care
HIGH
FDA DEVICE

Cardinal Health Salem Sump Stomach Tubes Recalled for ARV Breakage Risk (2025)

Cardinal Health recalled Salem Sump dual-lumen stomach tubes worldwide after ARV breakage complaints. The anti-reflux valve can break when excessive force is used. Healthcare providers and patients should stop using the device and follow recall instructions from the manufacturer.

Cardinal Health
Firm has
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical ESPOCAN Spinal/Epidural Tray Recalled Over Lid Position Risk

B Braun Medical recalled 10,130 ESPOCAN spinal/epidural trays nationwide after discovering potential for the catheter connector lid to be in an incorrect position. The recall covers multiple product codes and UDI numbers. Healthcare providers must stop using affected units and follow manufacturer instructions for remediation.

B BRAUN MEDICAL
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Cardinal Health 200 Recalls Salem Sump Dual-Lumen Stomach Tubes Over ARV Breakage (2025)

Cardinal Health 200 LLC expanded a worldwide recall of Salem Sump silicone dual-lumen stomach tubes after complaints of anti-reflux valve breakage. The valve can fracture under normal use, potentially compromising tube function. Healthcare providers and patients must stop using the device immediately and follow the manufacturer’s recall instructions.

Cardinal Health 200
Firm has
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Food & Beverages
HIGH
FDA FOOD

Goyal Group SILVER HORSE Aluminum Milk Pan & Mathar Kadaï Recalled for Lead Contamination (293 Sets,

Goyal Group Inc. recalled 293 sets of SILVER HORSE aluminum cookware, including a 4-inch milk pan and a 26-inch mathar kadai, distributed to customers in multiple states. The FDA enforcement report notes elevated lead levels in the products. Consumers should stop using the cookware and contact Goyal Group for a refund or replacement.

Goyal Group
Contains elevated
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems LOGIQ P10 Ultrasound System Recalled for UGAP Data Inaccuracy (31 Units, 2025)

GE Medical Systems recalled 31 LOGIQ P10 R4.5 HD ultrasound systems sold nationwide in the United States and globally after discovering UGAP measurements may misstate liver steatosis. The UGAP data may display inaccurate values representing liver steatosis. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions.

GE Medical Systems
The Ultrasound-Guided
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Food & Beverages
HIGH
FDA FOOD

Taproom Gourmet 15lb Bulk Madison Mix Recalled Over Undeclared Allergens

Taproom Gourmet recalled 3,547 cases of 15lb bulk Madison Mix after undeclared allergens were found. The recall cites no ingredient label as the defect. Consumers should not consume the product and should seek refund or replacement from Egress Capital Partners Inc.

Taproom Gourmet
No ingredient
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Health & Personal Care
HIGH
FDA DEVICE

Cardinal Health 200 Salem Sump Gastroduodenal Tubes Recalled Worldwide for ARV Breakage

Cardinal Health 200, LLC recalled Salem Sump gastroduodenal tubes worldwide after reports of anti-reflux valve breakage. The ARV can fail under excessive force during use. Healthcare providers and patients should stop using the device immediately and follow the manufacturer instructions for recall communication.

Cardinal Health 200
Firm has
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Food & Beverages
HIGH
FDA FOOD

Taproom Gourmet Bulk Fifth Avenue Mix Recalled for No Ingredient Label and Allergens

Taproom Gourmet recalled 3,547 cases of 18lb and 20lb bulk Fifth Avenue Mix sold in six states after undeclared peanuts, almonds, cashew, and soy were found. The recall classifies the hazard as HIGH. Consumers should discard the product or return for refund or replacement via Egress Capital Partners Inc.

Taproom Gourmet
No ingredient
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Food & Beverages
HIGH
FDA FOOD

Taproom Gourmet Bulk Empire Mix Recall for undeclared tree-nut Allergens

Taproom Gourmet bulk Empire Mix recall affects 3,547 cases distributed across New York, New Jersey, Connecticut, California, Illinois and Florida. The product lacks an ingredient label and contains undeclared allergens. Consumers should not consume the product and should seek a refund or replacement from Egress Capital Partners.

Taproom Gourmet
No ingredient
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Recall Expands for Perifix FX Epidural Tray and Catheter Over Lid Position Defect (Z

B Braun Medical recalled an epidural anesthesia tray nationwide after finding a lid misalignment in the catheter connector could occur. The recall involves the PERIFIX FX Continuous Epidural Anesthesia Tray and PERIFIX FX Springwound Catheter with a 17 Ga Tuohy needle and 19 Ga closed-tip catheter. The recall date is 2025-09-18 with report of ongoing action as of 2025-10-15. Healthcare providers,,

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DRUG

Glenmark Azelaic Acid Gel Recall Affects 13,824 Tubes Sold Nationwide in 2025

Glenmark Pharmaceuticals Inc. USA recalls 13,824 tubes of azelaic acid gel 15% after CGMP deviations prompted gritty texture complaints. The recall covers nationwide distribution in the United States. Consumers should stop using the product and contact Glenmark for guidance.

Glenmark Pharmaceuticals
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Enterix InSure ONE FIT Recall Affects 201,426 Tests Over False Negatives (2025)

Enterix recalled 201,426 InSure ONE Fecal Immunochemical Test kits after a sensitivity failure linked to Test Card Lot TT241102. The issue may cause false negative results. Healthcare providers and patients should stop using the affected kits and follow the manufacturer’s recall instructions.

Enterix
InSure ONE
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Tag Statistics

Total Recalls
915

Related Tags

infant productimmediate actionstop use immediatelyreplacement availablefda regulatedcpsc regulatedelectronicmetalplasticreturn for refundkitchenworkplace