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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
May 7, 2025Medical DevicesFDA
GE Medical Systems China Co., Ltd. recalls GE Healthcare Carestation 650c A1, Model/REF Number 1012-9655-200. Anesthesia system.
Hazard: Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.
May 7, 2025Medical DevicesFDA
GE Medical Systems China Co., Ltd. recalls GE Healthcare CARESTATION 650C A2, Model/REF Number 1012-9655-002. Anesthesia system.
Hazard: Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.
May 7, 2025Medical DevicesFDA
GE Medical Systems China Co., Ltd. recalls GE Healthcare CARESTATION 650C A1, Model/REF Number 1012-9655-000. Anesthesia system.
Hazard: Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.
May 7, 2025Medical DevicesFDA
GE Medical Systems China Co., Ltd. recalls GE Healthcare Carestation 650 A1, Model/REF Number 1012-9650-200. Anesthesia system.
Hazard: Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.
May 7, 2025Medical DevicesFDA
GE Medical Systems China Co., Ltd. recalls GE Healthcare Carestation 650 SE, Model/REF Number 1012-9650-012. Anesthesia system.
Hazard: Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.
May 7, 2025Medical DevicesFDA
GE Medical Systems China Co., Ltd. recalls GE Healthcare CARESTATION 650 A2, Model/REF Number 1012-9650-002. Anesthesia system.
Hazard: Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.
May 7, 2025Medical DevicesFDA
GE Medical Systems China Co., Ltd. recalls GE Healthcare CARESTATION 650 A1, Model/REF Number 1012-9650-000. Anesthesia system.
Hazard: Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.
May 7, 2025Medical DevicesFDA
GE Medical Systems China Co., Ltd. recalls GE Healthcare Carestation 620 A1, Model/REF Number 1012-9620-200. Anesthesia system.
Hazard: Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.
May 7, 2025Medical DevicesFDA
GE Medical Systems China Co., Ltd. recalls GE Healthcare Carestation 620 SE, Model/REF Number 1012-9620-012. Anesthesia system.
Hazard: Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.
May 7, 2025Medical DevicesFDA
GE Medical Systems China Co., Ltd. recalls GE Healthcare CARESTATION 620 A2, Model/REF Number 1012-9620-002. Anesthesia system.
Hazard: Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.
May 7, 2025Medical DevicesFDA
GE Medical Systems China Co., Ltd. recalls GE Healthcare CARESTATION 620 A1, Model/REF Number 1012-9620-000. anesthesia systems
Hazard: Certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems will not provide effective ventilation in Volume Control Ventilation (VCV) mode. In these systems, effective ventilation can be achieved in Pressure Control Ventilation (PCV) or Pressure Control Ventilation Volume Guarantee (PCV-VG) modes or with Manual ventilation.
May 7, 2025Food & BeverageFDA
Emily Kate's Foods recalls Emily Kate's Gluten Free Carrot Cake, Net Wt. 6.4oz, Emily Kate's Food, LLC, Kansas City, KS 66106, UPC 850581007284
Hazard: Foreign material (foil) found in cake slices
May 7, 2025Food & BeverageFDA
Emily Kate's Foods recalls Emily Kate's Gluten Free Vanilla Cake, Net Wt. 6.4oz, Emily Kate's Foods, Kansas City, KS 66106, UPC 850581007253
Hazard: Foreign material (foil) found in cake slices
May 7, 2025Food & BeverageFDA
MegaMex Foods LLC recalls La Victoria Cilantro Salsa; Med; Net Wt 15.5 OZ; UPC# 0 72101 34470 3; Distributed by: Megamex Foods, LLC Orange, CA 9
Hazard: Firm's salsa product was potentially manufactured with a recalled ingredient (Fresh Cilantro containing foreign objects "wood pieces")
May 7, 2025Food & BeverageFDA
Dinstuhl's Fine Candy Company, Inc. recalls Dinstuhl's Pecan Brittle, NET WT 4 oz. (113g), individually packaged in cellophane bags; Ingredients: Sugar, Pecans, Cor
Hazard: Undeclared allergen (milk)
May 7, 2025Food & BeverageFDA
Dinstuhl's Fine Candy Company, Inc. recalls Dinstuhl's Peanut Brittle, NET WT 4 oz. (113g), individually packaged in cellophane bags; Ingredients: Sugar, Corn Syrup
Hazard: Undeclared allergen (milk)
May 7, 2025Food & BeverageFDA
Dinstuhl's Fine Candy Company, Inc. recalls Dinstuhl's Cashew Crunch, NET WT 4 oz. (113g), individually packaged in cellophane bags; Ingredients: Sugar, Cashews, Co
Hazard: Undeclared allergen (milk)
May 7, 2025Food & BeverageFDA
Dianne's Fine Desserts recalls Outer carton labeled: "Cookie Butter Banana Pie" Inner carton labeled: "Tropical Key Lime Pie" Product contained inside
Hazard: Contains undeclared allergens (almonds).
May 7, 2025Food & BeverageFDA
Caraluzzi's Markets recalls Caraluzzi's Italian Style Seafood Burgers, 8oz; INGREDIENTS: Cod, Salmon, Shrimp, Scallops, Onions, Olive Oil, White Win
Hazard: Product contains undeclared egg.
May 7, 2025Food & BeverageFDA
Valley Fine Foods Co., Inc recalls CHILE VERDE EGG BITES; NET WT. 4.6 OZ (130 g); 2 egg bites/package
Hazard: Potential contamination with foreign materials.
May 7, 2025Food & BeverageFDA
Giant Eagle, Inc. recalls Multigrain Sourdough Freshly Backed, and Half Multigrain Sourdough Artisan Bread, 15 oz; 7 oz, Bag, 1 unit
Hazard: Firm is recalling product due to the potential of foreign material (glass)
May 7, 2025Food & BeverageFDA
Gordon Desserts DBA Mochidoki recalls Sundae Shoppe, Cookies and Cream Mochi Ice Cream, 6 count, 7.5 oz, Plastic sealed tray inside paper carton. 6 Pieces pe
Hazard: Undeclared Wheat and Soy
May 7, 2025Food & BeverageFDA
Upper Crust Bakery LP recalls Whole Grain Multigrain , 20 oz, Paper carton (corrugated), CP12, Frozen
Hazard: Glass fragment found on top of bread.
May 7, 2025Food & BeverageFDA
Upper Crust Bakery LP recalls Multigrain Sourdough , 18 oz, Paper carton (corrugated), CP12, Frozen
Hazard: Glass fragment found on top of bread.
May 7, 2025Food & BeverageFDA
Upper Crust Bakery LP recalls Ancient Grains Hoagie Roll, 4 oz, Paper carton (corrugated), CP45, Frozen
Hazard: Glass fragment found on top of bread.
May 7, 2025DrugsFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls Infuvite Adult, multiple vitamins injection, Baxter, Five of Vial 1 (5 mL) and Five of Vial 2 (5mL), Rx Only, Sterile, M
Hazard: Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.
May 7, 2025DrugsFDA
Mckesson Medical-Surgical Inc. Corporate Office recalls Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Vial, Rx only, Mfd. in India for:
Hazard: Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.
May 7, 2025DrugsFDA
American Regent, Inc. recalls niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial, Rx Only, American Regent, Inc
Hazard: Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
May 7, 2025DrugsFDA
American Regent, Inc. recalls niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial, Rx Only, Mfd for: Civica, Inc
Hazard: Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
May 7, 2025DrugsFDA
ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 90 bottles, Rx Only, Manufactured for Accord Healthcare, Inc., Ra
Hazard: Subpotent