All Product Recalls

Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Recalled IcyBreeze Buddy Portable Misting Fan in slate blue
HIGH
CPSC

IcyBreeze Recall Expands Over Fire Hazard Risk in Portable Misting Fans (2025)

IcyBreeze recalled the IcyBreeze Buddy portable misting fan due to a charging fire hazard. The recall affects consumers who own the IcyBreeze Buddy with a 1.5-liter water tank and a 10,000 mAh lithium-ion battery. Affected units must be returned for a full refund and disposal guidance. Call 817-900-2664 or visit the recall page to begin the process and receive a $150 credit at Solo Brands brands.

IcyBreeze Cooling
The misting
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical PERIFIX FX Epidural Set Recalled for Lid-Position Defect in 2025

B Braun Medical recalls the PERIFIX FX Continuous Epidural Anesthesia Set and PERIFIX Tuohy Epidural Needle nationwide after a lid-position defect is identified. The issue involves the lid of the catheter connector being in the incorrect position. Healthcare providers are advised to stop using the device and follow the manufacturer’s recall instructions.

B Braun Medical
Potential for
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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

GE Medical Systems LOGIQ P9 R4.5 Ultrasound System Recalled for Inaccurate Liver Readings (37 Units)

GE Medical Systems recalled 37 LOGIQ P9 R4.5 ultrasound systems sold nationwide in the United States and globally after regulators flagged UGAP measurements that may misrepresent liver steatosis. The UGAP data may display inaccurate values representing liver steatosis, potentially guiding inappropriate clinical decisions. Clinicians should stop using the affected devices and await recall guidance.

GE Medical Systems
The Ultrasound-Guided
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Health & Personal Care
HIGH
FDA DEVICE

HeartSine Pad-Pak Defibrillator Pads Recalled for 1,291,165 Units in 2025

HeartSine Technologies recalled 1,291,165 Pad-Pak defibrillator pads sold nationwide in the United States and worldwide. A defect may allow damage pins to disrupt the mechanical fit and electrical contact. Stop using the pads immediately and follow the manufacturer's recall instructions.

HeartSine Technologies
Due to
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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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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

Cook Medical Zenith Alpha 2 Thoracic Graft Recall Affects 695 Devices in 2025

Cook Medical recalled 695 Zenith Alpha 2 Thoracic Endovascular Grafts distributed to hospitals domestically and internationally. A defect could cause PTFE coating scrapings to be released during deployment, risking intravascular embolization. Healthcare providers and patients should stop using the device and follow the manufacturer’s recall instructions.

Cook Medical
Affected devices
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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

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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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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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical PERIFIX FX Epidural Tray Recalled for Lid Misalignment in 48,110 Units (2025)

B Braun Medical Inc. recalled 48,110 units of the PERIFIX FX Continuous Epidural Anesthesia Tray nationwide to hospitals and surgical centers. The recall cites a potential for the lid of the catheter connector to be in the incorrect position. Hospitals and clinics should stop using the device and contact B Braun Medical for instructions.

B Braun Medical
Potential for
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