794 recalls tagged with “infant product”.
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.
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.
Taproom Gourmet brand bulk Broadway Mix recall covers 3,547 cases distributed across six states. The recall cites no ingredient label and undeclared allergens including peanuts, sesame, wheat and soy. Consumers should not consume the product and should seek refund or replacement through Egress Capital Partners Inc.
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.
Cardinal Health 200 recalled Salem Sump dual-lumen stomach tubes worldwide after complaints that the anti-reflux valve breaks under normal use. The ARV breakage can compromise tube function. Hospitals and providers should stop using the devices and follow recall instructions immediately.
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 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.
Fisher & Paykel Healthcare recalled 51,144 Airvo 2 and myAirvo 2 humidifiers in the United States. The devices may emit an audible alert for less than 120 seconds after power is disconnected. This could delay user awareness to reconnect power and lead to oxygen desaturation. Patients and healthcare providers should stop using the device and await manufacturer instructions.
B BRAUN MEDICAL INC recalls 5,770 PERIFIX FX Epidural Anesthesia Trays nationwide after a potential lid misalignment in the catheter connector. The issue could affect catheter administration. Stop using the device and follow recall instructions immediately. Healthcare providers should contact B Braun for guidance.
B Braun Medical recalled 2,450 SESK pain management trays distributed nationwide. The recall cites a potential mispositioned catheter connector lid, classified as Class II with high hazard. Patients and healthcare providers were advised to stop using the device and follow recall instructions.
Kirkland Signature Ahi Tuna Wasabi Poke sold at Costco is recalled after a Listeria monocytogenes positive test in green onions used in the product. Western United Fish Company initiated the recall. Consumers should not eat the product and should seek refunds or replacements.
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.
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,,
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.
B BRAUN MEDICAL INC recalls 2,760 units nationwide due to a lid misalignment risk in the catheter connector. The recall covers the PERIFIX FX Continuous Epidural Anesthesia Tray and related components. Healthcare providers should halt use and follow manufacturer instructions for recall remedies.
B BRAUN MEDICAL INC recalls 60 units of SESK Combined Spinal and Epidural Tray nationwide. The recall targets products distributed to all 50 states. The defective lid on the catheter connector may be in the incorrect position, posing a high-risk device issue. Stop using immediately and follow company instructions for recall remedies.
B Braun Medical has an active recall of the PERIFIX FX Continuous Epidural Anesthesia Tray nationwide. The recall cites a potential mispositioned catheter connector lid. Healthcare providers and patients should stop using the device and follow manufacturer instructions.
Taproom Gourmet bulk Park Mix, distributed to NY, NJ, CT, CA, IL and FL, is recalled for undeclared allergens and no ingredient label. Consumers should not consume the product. Egress Capital Partners Inc. is handling refunds or replacements via email.
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.
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.