Safety Recalls
RSS ↗17,560 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 5,051–5,100 of 17,560
- Class II
- Class II
Medical Device Recall · November 3, 2025
Urinary Tract Infection TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Food Intolerance Test SmallDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
D-Dimer TestDistribution without premarket approval/clearance.
- Unclassified
Vehicle Recall · November 3, 2025
2023 VOLVO VAHA seat belt anchor that fails will not properly restrain an occupant in a crash, increasing the risk of injury.
- Class II
Medical Device Recall · November 3, 2025
Diabetes HbA1c TestDistribution without premarket approval/clearance.
- Class III
Medical Device Recall · November 3, 2025
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 II
Medical Device Recall · November 3, 2025
Lactose Intolerance TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Parasite TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Sperm TestDistribution without premarket approval/clearance.
- Class II
- Unclassified
Vehicle Recall · November 3, 2025
2025 MACK GRANITE (GR)Loss of headlight illumination can reduce visibility, increasing the risk of a crash.
- Class II
Medical Device Recall · November 3, 2025
Illegally MarketedDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Drug Test Small (4 substances)Distribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Parasite TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Organic acids TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Adrenal TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Cholesterol TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Sperm TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Mycoplasma test, IgG and IgMDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Pollen Allergy TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Ivenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004.Downstream Occlusion alarms may occur during procedures using low flow infusion rates when a check valve* is added to the Ivenix Administration Set.
- Class II
Medical Device Recall · November 3, 2025
Alcohol (ALC) Test SalivaDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Pet Allergy TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Gut Microbiome Test SmallDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
8 in 1 STI Test KitDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 2, 2025
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, whoseA 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
Food Recall · October 31, 2025
INDIAN COOKWARE AND APPLIANCE LLC
ALUMINIUM HAMMERED KADAI SIZE 7 8 901000 000057 MADE IN INDIAPotential contamination due to leachable lead.
- Class II
Medical Device Recall · October 31, 2025
Stryker Medical Division of Stryker Corporation
Stryker Arise 1000EX mattress, Part Number 2236000000Stryker 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
Medical Device Recall · October 31, 2025
NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita; NN-8026 BrainPath Shephard's Hook - Budde; NN-8042 BraTape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX800. Product Number: 865240.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP - MINOP; NN-8003 13x10 MHP; NN-8004 13x13 MHP; NN-8005 15x25 MHP GAAB; NTape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
- Class II
Medical Device Recall · October 31, 2025
Stryker Medical Division of Stryker Corporation
Stryker MV3 bariatric bed, Part Number 5900000001Stryker 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
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX500. Product Number: 866064.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
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
Drug Recall · October 31, 2025
Dynashield, 4 oz cream (113 g), Manufactured for: Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10852, USA, Made in India, NDC 67777-407-03.cGMP deviations
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX550. Product Number: 866066.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
OraVerse, (Phentolamine Mesylate) Injection, 0.4 mg/1.7mL, packaged in a carton containing 10 cartridges, 0.4 mg/1.7mL, Rx only, Made in Canada by Novocol Pharmaceutical of Canada, Inc., Distributed bDefective container: cracked/broken cartridges
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP50. Product Number: M8004A.Potential issue where the IntelliVue monitors did not alarm.
- Unclassified
Vehicle Recall · October 31, 2025
2025 MICRO BIRD G5 SCHOOL BUSAn unlocked wheelchair can move during transit or during a crash, increasing the risk of injury.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Multi-Measurement Module X3. Product Number: 867030.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP2. Product Number: M8102A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
Olympus OER-EliteInform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
Cook-Walte, Carbocaine 3% (30 mg/mL), (mepivacaine hydrochloride Injection, USP), packaged in a carton containing 50 Single-Dose Cartridges, 1.7 mL, Rx only, Manufactured by Novocol Pharmaceutical ofDefective container: cracked/broken cartridges
- Class II
Drug Recall · October 31, 2025
Dynashield Skin Protectant, Net Wt. 16 oz (453.6 g), Manufactured for: Dyrnarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962, USA, Made in India, NDC 67777-407-04.cGMP deviations
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
Benco dental Graham CHEMICAL CO., Mepivacaine HCI 3% (30 mg/mL) Injection, [Mepivacaine HCI Injection, USP], packaged in a carton containing 50 single-dose Cartridges, 1.7 mL each, Rx only, DistributeDefective container: cracked/broken cartridges
- Class II
Medical Device Recall · October 31, 2025
NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illumination Sleeve/FiberTape used to secure components within packaging contains latex, despite products being labeled as latex-free. Latex could potentially cause an allergic reaction.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX750. Product Number: 866471.Potential issue where the IntelliVue monitors did not alarm.