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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
August 20, 2025Medical DevicesFDA
Spark Biomedical Inc recalls Sparrow Ascent Patient Controller, REF's: 11-110-K, 11-310-K, 11-320-K, 11-321-K, 11-310-K-28, 11-320-K-28, 11-321-K-28
Hazard: Due to manufacturing issue, neurostimulator device may experience "cable disconnect" error message and interruption to stimulation output.
August 20, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 7R 16MM, VE Model/Catalog Number: 34
Hazard: Knee implants contain incorrect labeling (size and/or side incorrect)
August 20, 2025Medical DevicesFDA
Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 4L 16MM, VE Model/Catalog Number: 34
Hazard: Knee implants contain incorrect labeling (size and/or side incorrect)
August 20, 2025Medical DevicesFDA
Carefree Surgical Specialties recalls Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Roll Gauze + Tail Medium 4 Long X-
Hazard: Due to two issues: 1. Product contamination (biological foreign matter) that could compromise sterility. 2. Incorrect quantity of gauze in sterile packaging
August 20, 2025Medical DevicesFDA
Carefree Surgical Specialties recalls Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray D
Hazard: Due to two issues: 1. Product contamination (biological foreign matter) that could compromise sterility. 2. Incorrect quantity of gauze in sterile packaging
August 20, 2025Medical DevicesFDA
Carefree Surgical Specialties recalls Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray D
Hazard: Due to two issues: 1. Product contamination (biological foreign matter) that could compromise sterility. 2. Incorrect quantity of gauze in sterile packaging
August 20, 2025Medical DevicesFDA
Carefree Surgical Specialties recalls Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray Detectab
Hazard: Due to two issues: 1. Product contamination (biological foreign matter) that could compromise sterility. 2. Incorrect quantity of gauze in sterile packaging
August 20, 2025Medical DevicesFDA
SPINEART SA recalls Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 55 45-S
Hazard: Cannulated fenestrated polyaxial screws may be incorrectly labeled
August 20, 2025Medical DevicesFDA
SPINEART SA recalls Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 65 40-S
Hazard: Cannulated fenestrated polyaxial screws may be incorrectly labeled
August 20, 2025Medical DevicesFDA
Boston Scientific Corporation recalls FARAWAVE 1.0 Pulsed Field Ablation Catheter, Product ID M004PF41M401
Hazard: The potentially impacted units were manufactured using specific equipment that may have caused cracks in the electrode bands on the catheter's distal end.
August 20, 2025Medical DevicesFDA
Boston Scientific Corporation recalls Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent, stent and stent delivery system. Material
Hazard: Certain batches are being removed due to an increase in complaints received in which physicians encountered greater than anticipated resistance while attempting to withdraw the stent delivery system (SDS) from the guidewire or embolic protection device (EPD) after successful stent deployment. The most serious potential adverse health consequence is stroke. Other risks include delay to procedure, vessel injury, vessel spasm, or stent disruption/damage necessitating additional intervention.
August 20, 2025Medical DevicesFDA
Philips Respironics, Inc. recalls DreamStation Auto. Non-Continuous Ventilator.
Hazard: Devices may possess a programming error resulting in an incorrect device configuration.
August 20, 2025Medical DevicesFDA
Philips Respironics, Inc. recalls DreamStation Auto BiPAP. Non-Continuous Ventilator.
Hazard: Devices may possess a programming error resulting in an incorrect device configuration.
August 20, 2025Medical DevicesFDA
Philips Respironics, Inc. recalls DreamStation Auto CPAP. Non-Continuous Ventilator.
Hazard: Devices may possess a programming error resulting in an incorrect device configuration.
August 20, 2025Medical DevicesFDA
Ambu Inc. recalls Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR II Adult Re
Hazard: Potential for the manometer port being blocked rendering the manometer non-functional.
August 20, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Novum IQ Large Volume Pump, Product Code REF 40700BAXUS
Hazard: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ large volume pump (LVP) due to the potential for underinfusion when transitioning from a flow rate to a higher flow rate that is more than double. (e.g., rate change or bolus). The level of underinfusion is variable based on the current infusion rate, the duration the pump has been running at this flow rate, and the magnitude of the rate change. The longer the duration the pump has been running at the current infusion rate and the larger the magnitude of the rate change, the larger the underinfusion that would be experienced. Additionally, Baxter has identified an increase in customer reports of over and underinfusion potentially due to set misloading. Failure to properly load the tubing into the pump channel may result in the pump infusing at a rate higher or lower than programmed. Consistent with the instructions for use, customers should ensure that: 1) The door is fully open before loading the set. 2) The tubing is taut and loaded without slack in the pumping channel.
August 20, 2025Food & BeverageFDA
Reser's Fine Foods, Inc. recalls Molly's Kitchens Tuna Salad, item 794599, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tu
Hazard: Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
August 20, 2025Food & BeverageFDA
Reser's Fine Foods, Inc. recalls Reser's Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in white plastic tub and lid with sticker. Keep R
Hazard: Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
August 20, 2025Food & BeverageFDA
Reser's Fine Foods, Inc. recalls Sysco Classic Tuna Salad, Reorder #6724249, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic
Hazard: Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
August 20, 2025Food & BeverageFDA
Reser's Fine Foods, Inc. recalls Sysco Imperial Deluxe Tuna Salad, Reorder #6526826, net wt. 5lb. Foodservice item. Product is packaged in clear printed
Hazard: Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
August 20, 2025Food & BeverageFDA
Reser's Fine Foods, Inc. recalls Reser's Gourmet Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with white l
Hazard: Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
August 20, 2025Food & BeverageFDA
Reser's Fine Foods, Inc. recalls Reser's Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in white plastic tub and lid with sticker. Keep R
Hazard: Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
August 20, 2025Food & BeverageFDA
Reser's Fine Foods, Inc. recalls Signature Cafe Premium Tuna Salad, net wt. 3lb (48oz). Foodservice item to be used by deli. Product is packaged in clear
Hazard: Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
August 20, 2025Food & BeverageFDA
Quesito El Establo recalls Quesito El Establo brand Spanish Cheese QUESITO COLOMBIANO; INGREDIENTS: Milk, Cheese Cultures, Salt, Vitamins C and D;
Hazard: Product was manufactured and held under insanitary conditions. Product may be contaminated with Listeria monocytogenes.
August 20, 2025Food & BeverageFDA
Jayone Foods, Inc. recalls Frozen Oyster Meat (IQF), Cert No. KR-15-SP; Processor Name: JBR KR-15-SP; Harvest Date: Feb 06, 2025 Shucked Date: Feb
Hazard: Frozen Oyster product is potentially contaminated with Norovirus
August 20, 2025Food & BeverageFDA
Jayone Foods, Inc. recalls Frozen Oyster Meat (IQF), Cert No. KR-15-SP; Processor Name: JBR KR-15-SP; Harvest Date: Feb 06, 2025 Shucked Date: Feb
Hazard: Frozen Oyster product is potentially contaminated with Norovirus
August 20, 2025Food & BeverageFDA
Dollar General Corporation recalls Clover Valley Instant Coffee, NET WT 8 OZ (227 g), packaged in a glass jar, packed 6 jars per case, UPC: 876941004069, D
Hazard: Potential presence of glass pieces
August 20, 2025Food & BeverageFDA
QST Ingredients and Packaging recalls Cajun Seasoning (Taratino) NET WT: 50 lb Usage: 13.80 LBS for 300 LBS of Meat UPC (QST# 4546)
Hazard: Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
August 20, 2025Food & BeverageFDA
QST Ingredients and Packaging recalls Lemon Pepper Seasoning (Tarantino) NET WT: 50 lb UPC (QST# 6402)
Hazard: Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
August 20, 2025Food & BeverageFDA
QST Ingredients and Packaging recalls BBQ Riblet Seasoning (Cargill Meat)(PPM) NET WT: 50 lb UPC (QST# 5275)
Hazard: Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.