HIGH
FDA DEVICE
Mesh Style Tip Protectors CSW-03-2.0 Open-end style CSW-04-4.0 Closed-end style
Product does not have FDA clearance.
Healthmark Industries Co.
Product does
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
High Risk Recalls
4,267 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
- High-risk recalls
- 4,267
- Action level
- Stop use
What to do if you own a recalled product
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
HIGH
HIGH
FDA FOOD
Yunker(branded) Energy & Health Herbal Supplement with Vitamins; Manufactured by Sato Pharmaceuticals Co. Ltd.; 30ml container. Packed in single serving, 3 units/pack, and 10 units per pack. Single...
Product does not meet label claim for Vitamin E.
Sato Pharmaceutical
Product does
HIGH
CPSC
17 Stories Furniture Dressers Recalled Over Tip-Over Risk
Online at Wayfair.com from September 2023 through January 2026 for about $135.
The recalled
HIGH
CPSC
LIVEHOM Dressers Recalled Over Tip-Over Hazard Risk
LIVEHOM recalled 11-Drawer Dressers on March 12, 2026, due to tip-over hazards. The recall affects dressers sold on Amazon that can pose serious risks to children. Consumers must stop using these dressers immediately and contact the company for a full refund.
LIVEHOM 11-Drawer Dressers
The recalled
HIGH
CPSC
ProRider Recalls Bicycle Helmets Over Serious Head Injury Risk
ProRider recalled several models of bicycle helmets on March 12, 2026, due to a serious risk of head injury. The helmets do not meet mandatory safety standards and can fail in a crash. Consumers should stop using these helmets immediately and seek a refund.
ProRider
The recalled
HIGH
HIGH
FDA DRUG
0.9% Sodium Chloride Injection, USP, 0.9% (900 mg per 100 mL) (9 mg per mL) 100 mL in a 100 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 600047, Unit of Use...
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
HIGH
FDA DRUG
0.9% Sodium Chloride Injection, USP, 50 mL x60, Becton, Dickson and Company, 1 Beckton Drive, Franklin Lakes, NJ 07417 USA, Distributed by BD, Manufactured by Fresenius Kabi USA, LLC ("Fresenius...
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Vehicles & Parts
HIGH
NHTSA
Honda Recalls 2023-2025 Pilot and 2023-2024 Passport Over Fuel Tank Filler Leakage (2026)
Honda (American Honda Motor Co.) is recalling certain 2023-2024 Passport and 2023-2025 Pilot vehicles. The fuel filler neck tube and fuel filler pipe may separate, allowing fuel to leak.
Honda
A fuel
Food & Beverages
HIGH
FDA FOOD
Lone Star Dairy Products Recalls 1.79M Lbs Spray Dried Dairy Powder Over Salmonella Risk (2026)
Salmonella spp. identified in finished product testing
Lone Star Dairy Products
Salmonella spp.
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 5% Dextrose Injection Recall for Sterility Concerns (2026) Affecting US Nationwide, R
Lack of Assurance of Sterility
DEXTROSE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 0.9% Sodium Chloride Injection Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 0.9% Sodium Chloride Injection Recalled for Lack of Sterility Assurance
Fresenius Kabi USA recalls 0.9% Sodium Chloride Injection units distributed nationwide, including Alaska and Puerto Rico. The recall cites lack of assurance of sterility. Healthcare providers should stop use and contact Fresenius Kabi for guidance.
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
BD and Fresenius Kabi 1,000 mL Sodium Chloride Injection Recall for Sterility Concerns (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi Saline Solution Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
BD and Fresenius Kabi Sodium Chloride Injection Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
HIGH
FDA DRUG
0.45% Sodium Chloride Injection, USP, 1.125 grams per 250 mL (4.5 mg per mL), 250 mL in a 250 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use...
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
HIGH
FDA DRUG
0.9% Sodium Chloride Injection, USP 900 mg per 100 mL (9 mg per mL) 500 mL in a Single Dose freeflex bag, 500 mL x 20, Manufactured for: Fresenius Kabi USA, LLC ("Fresenius Kabi"), IL 60047, Unit of...
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
HIGH
FDA DRUG
0.9% Sodium Chloride Injection, USP, (4,500 mg per 500 mL) (9 mg per mL) 500 mL in a 500 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC:...
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of