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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
July 9, 2025Medical DevicesFDA
Onkos Surgical, Inc. recalls My3D Personalized Solutions Humeral Cup, Model Number: C24-0223-0003. It is a component of a Custom Constrained Sho
Hazard: Required inspections were not performed on finished product prior to release and distribution.
July 9, 2025Medical DevicesFDA
Hardy Diagnostics recalls HardyCHROM CRE, selective and differential culture medium for antimicrobial susceptibility testing, Product Catalog No.
Hazard: Identified lots failed incoming quality control testing. Lots exhibited breakthrough growth of Klebsiella pneumoniae.
July 9, 2025Medical DevicesFDA
Ortho-Clinical Diagnostics, Inc. recalls Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog Number: (1) 6802445, (2) 6900440 Software
Hazard: a software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not enabled if a shelf expiration date is omitted during manual loading. The issue was identified by a customer complaint, in which a CREA Urine test was processed with an RE (Reagent Expired) code, even though the diluent pack was not expired and the use-expired-reagents setting was disabled. This can result in erroneous test results and/or delaying test results.
July 9, 2025Medical DevicesFDA
Ortho-Clinical Diagnostics, Inc. recalls Brand Name: VITROS; Product Name: VITROS XT 7600 Integrated System; Model/Catalog Number: (1) 6844461, (2) 6272222; S
Hazard: a software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not enabled if a shelf expiration date is omitted during manual loading. The issue was identified by a customer complaint, in which a CREA Urine test was processed with an RE (Reagent Expired) code, even though the diluent pack was not expired and the use-expired-reagents setting was disabled. This can result in erroneous test results and/or delaying test results.
July 9, 2025Medical DevicesFDA
Ortho-Clinical Diagnostics, Inc. recalls Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog Number: (1) 6802413, (2) 6802915
Hazard: A software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not enabled if a shelf expiration date is omitted during manual loading. The issue was identified by a customer complaint, in which a CREA Urine test was processed with an RE (Reagent Expired) code, even though the diluent pack was not expired and the use-expired-reagents setting was disabled. This can result in erroneous test results and/or delaying test results.
July 9, 2025Medical DevicesFDA
Philips Respironics, Inc. recalls BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric pa
Hazard: This device does not indicate for use in patients with respiratory failure.
July 9, 2025Medical DevicesFDA
Philips Respironics, Inc. recalls BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support in adult and pediatric patients weighing more
Hazard: This device does not indicate for use in patients with respiratory failure.
July 9, 2025Medical DevicesFDA
Philips Respironics, Inc. recalls BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighin
Hazard: This device does not indicate for use in patients with respiratory failure.
July 9, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls interventional fluoroscopic x-ray system
Hazard: In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose.
July 9, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls interventional fluoroscopic x-ray system
Hazard: In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose.
July 9, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls interventional fluoroscopic x-ray system
Hazard: In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose.
July 9, 2025Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and intervention
Hazard: In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose.
July 9, 2025Medical DevicesFDA
Maquet Critical Care AB recalls Servo-u MR Ventilator System. Model Number: 6888800.
Hazard: Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.
July 9, 2025Medical DevicesFDA
Maquet Critical Care AB recalls Servo-n Ventilator System. Model Number: 6694800.
Hazard: Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.
July 9, 2025Medical DevicesFDA
Maquet Critical Care AB recalls Servo-u Ventilator System. Model Number: 6688600.
Hazard: Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.
July 9, 2025Food & BeverageFDA
FUENTES FARMS LLC recalls Cucumbers Box 40Lbs 1 1/9 Bushels.
Hazard: Cucumbers have the potential to be contaminated with Salmonella
July 9, 2025Food & BeverageFDA
Vita Warehouse Corp. recalls 1. Welby Vitamin B12 Adult Gummies 140 Count 2. Berkely Jensen¿ Vitamin B12 1000 mcg Gummies 250 count 3. VitaGlobe" Vit
Hazard: Contains undeclared peanut
July 9, 2025Food & BeverageFDA
Meijer, Inc #816 - Grand River Packaging recalls Frederik's by Meijer Dark Chocolate Almonds 12 oz. resealable bag, UPC 7 08820 68730 1, 6 retail units per wholesale cas
Hazard: undeclared cashews
July 9, 2025Food & BeverageFDA
August Egg Company recalls --- Shell Eggs; Brown; Various sizes - medium, large, and jumbo; Various pack sizes - 5, 12, 18, and Loose ---- Clover
Hazard: Potential contamination with Salmonella.
July 9, 2025Food & BeverageFDA
JFE FRANCHISING INC recalls Yaki Noodle Bowl 12 oz 63912389254 Ebi Vermicelli Bowl 13oz 63912389334
Hazard: Cucumbers have the potential to be contaminated with Salmonella.
July 9, 2025Food & BeverageFDA
JFE FRANCHISING INC recalls Bibimbap Bowl 13 oz 63912389259
Hazard: Cucumbers have the potential to be contaminated with Salmonella.
July 9, 2025Food & BeverageFDA
JFE FRANCHISING INC recalls Fruit & Vegetable Tray - 64 oz 63912394047 Mixed Melon, Cucumbers & Tajin - 18oz 63912394007 Watermelon & Cucumber
Hazard: Cucumbers have the potential to be contaminated with Salmonella.
July 9, 2025Food & BeverageFDA
JFE FRANCHISING INC recalls Cucumber with Ranch - 9 oz 63912395020 Cucumber, Lime & Tajin - 19oz 63912388053 Cucumber Slices w/Tajin - 15 oz
Hazard: Cucumbers have the potential to be contaminated with Salmonella.
July 9, 2025Food & BeverageFDA
JFE FRANCHISING INC recalls Family Garden Salad - 24 oz 63912388065 Garden Salad - 12 oz 63912388067 Family Cobb Salad - 22 oz 63912388068 Cobb S
Hazard: Cucumbers have the potential to be contaminated with Salmonella.
July 9, 2025Food & BeverageFDA
Alma Pak International LLC recalls FROZEN ORGANIC BLUEBERRIES, INGREDIENTS: FROZEN ORGANIC BLUEBERRIES 30# Bulk Blueberries ALMA PAK INTERNATIONAL, LLC 230
Hazard: Listeria monocytogenes. During routine testing the firm received positive test results of Listeria monocytogenes on their finished product.
July 9, 2025Food & BeverageFDA
Peak Cocktails recalls Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24,
Hazard: Overpressurization leading to exploding cans
July 9, 2025Food & BeverageFDA
Harris Teeter recalls ZENSHI HANDCRAFTED SUSHI California Roll 10pc (Brown Rice) Net Wt. 7.1oz UPC 0 23012 94265 6 & UPC 0 23012 95137 5
Hazard: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
July 9, 2025Food & BeverageFDA
Harris Teeter recalls ZENSHI HANDCRAFTED SUSHI Yuzu Teriyaki Tuna Roll 10pc Net Wt. 3oz UPC 0 23012 95033 0
Hazard: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
July 9, 2025Food & BeverageFDA
Harris Teeter recalls ZENSHI HANDCRAFTED SUSHI Yuzu Teriyaki Sauce 3oz Net Wt. 3oz UPC 0 23012 95076 7
Hazard: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
July 9, 2025Food & BeverageFDA
Harris Teeter recalls ZENSHI HANDCRAFTED SUSHI Vegetable Roll 10pc (Brown Rice) Net Wt. 7.1oz UPC 0 23012 94328 8 & UPC 0 23012 95152 8
Hazard: Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.