Safety Recalls

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15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

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Showing 3,451–3,500 of 15,186

Medical Device Recall · November 3, 2025
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Adrenal Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Gut Microbiome Test Mega
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Environmental Pollutants Profile Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Continuous Glucose Monitor (CGM)
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
GVS TM, Inc
SQ40S Blood Transfusion Filter
Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed.
Class II
Medical Device Recall · November 3, 2025
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Food Intolerance Test Small
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Pregnancy Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Allergy & Food Intolerance Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Epstein-Barr Virus (EBV VCA & EBNA IgG) Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Diabetes HbA1c Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Mycoplasma test, IgG and IgM
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Melatonin Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Ovulation Test (5 tests)
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Sorbitol Intolerance Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Iodine Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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GI Microbiome Profile XL
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
Orthofix U.S. LLC
Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System Model/Catalog Number: 39-9012SP 33W X 28L X 12.5H, 7DEG PTC IMPLANT; 39-9014SP 33W X 28L X 14H, 7DEG PTC IMPLANT;
Labeling contains claims that are not consistently present.
Class III
Medical Device Recall · November 3, 2025
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Illegally Marketed
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Food Sensitivity Test Small
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Parasite Test
Distribution without premarket approval/clearance.
Class II
Food Recall · November 3, 2025
Dough-To-Go Inc
Linzer Hearts Baked Cut Out Cookies UPC 0 44964 22072 2 72 - 4.0 oz Cut Cookies CBB-220-LZ Net Weight: 18 lbs Ingredients: Enriched flour (bleached WHEAT flowr, malted barley flour, niacin, iron, thai
Undeclared Milk and FD&C Blue #1.
Class II
Medical Device Recall · November 3, 2025
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Sperm Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
Orthofix U.S. LLC
Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model/Catalog Number: 18-1025SP 11mm X 25mm FIREBIRD SI Screw; 18-1030SP 11mm X 30mm FIREBIRD SI Screw; 18-1035SP 11
Labeling contains claims that are not consistently present.
Class III
Medical Device Recall · November 3, 2025
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Organic Acids Profile Test Large
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Neurotransmitters Plus
Distribution without premarket approval/clearance.
Class II
Food Recall · November 3, 2025
Dreyer's Grand Ice Cream, Inc.
Retail Box: Haagen-Dazs mini chocolate dark chocolate ice cream bars 6 BARS/11.1 FL/OZ(328mL) INGREDIENTS: CHOCOLATE ICE CREAM: CREAM, SKIM MILK, SUGAR, COCOA PROCESSED WITH ALKALI, EGG YOLKS. DARK CH
Undeclared wheat.
Class II
Medical Device Recall · November 3, 2025
GE Healthcare GmbH
GE HealthCare ViewPoint 6, Catalog Number H47601AA; Radiological image processing system
GE HealthCare has become aware that the Patient History tab in ViewPoint 6 versions 6.15.3 and 6.15.4 ultrasound software may not include complete patient medical history information.
Class II
Medical Device Recall · November 3, 2025
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Food Sensitivity Test Large
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Allergy test Small
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Heavy Metals Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Intestinal Worms Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Candida Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
Orthofix U.S. LLC
Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer System Model/Catalog Number: 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6005SP 12mm W X 12mm L, 5mm H, 5¿
Labeling contains claims that are not consistently present.
Class III
Medical Device Recall · November 3, 2025
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DHEA Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Serotonin Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
Orthofix U.S. LLC
Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number: 37-3106SP 12mm W X 12mm L, 6mm H, Parallel; 37-3107SP 12mm W X 12mm L, 7mm H, Par
Labeling contains claims that are not consistently present.
Class III
Medical Device Recall · November 3, 2025
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Food Allergy Panel Test (IgE)
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Food Intolerance Test Large
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Vitamin D2 and D3 Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Leaky Gut Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Menopause (FSH) 2 Tests
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Lyme Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Organic acids Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Chlamydia Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 3, 2025
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Cholesterol Test
Distribution without premarket approval/clearance.
Class II
Medical Device Recall · November 2, 2025
Medtronic MiniMed, Inc.
MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump is indicated for use by patients age 7-80 years with Type 1 diabetes, whose
A software timing and processor communication issue in MiniMed" 780G software version 6.60 may trigger Pump Error 43 and/or Pump Error 41, resulting in suspension of insulin delivery.
Class II
Drug Recall · October 31, 2025
Blossom Pharmaceuticals
Globe Clotrimazole Cream, USP, 1 %, Net Wt. 1 oz (28.4g), Distributed by: Trifecta Pharmaceuticals USA, 101 NE Third Avenue, Suite 1500, Ft. Lauderdale, FL 33301 USA, Made in India, NDC 69396-087-01.
cGMP deviations
Class II
Drug Recall · October 31, 2025
Blossom Pharmaceuticals
Globe Zinc Oxide Ointment USP Zinc Oxide 20% Skin Protectant, Net Wt. 2 oz (56.7 g), Distributed by: Trifecta Pharmaceuticals USA 101 NE, Third Avenue, Suite 1500, Ft. Lauderdale, FL 33301, NDC 69396-
cGMP deviations
Class II
Medical Device Recall · October 31, 2025
Stryker Medical Division of Stryker Corporation
Stryker MV3 bariatric bed, Part Number 5900000001
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.
Class II
Drug Recall · October 31, 2025
Blossom Pharmaceuticals
Nivagen, Zinc Oxide Ointment USP, Zinc Oxide 20 %, Net Wt. 1 oz. (28.4g), Nivagen Pharmaceuticals, Inc., Sacramento, CA 95827, USA, Made in India, NDC 75834-170-02.
cGMP deviations
Class II