Safety Recalls
RSS ↗15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 3,351–3,400 of 15,186
- Unclassified
Vehicle Recall · November 6, 2025
2025 RIVIAN R1T, 2025 RIVIAN R1STurn signals that do not function properly, failing to indicate the driver's intention to change direction, increase the risk of a crash.
- Class II
Medical Device Recall · November 6, 2025
Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
- Unclassified
Consumer Product Recall · November 6, 2025
F&F Fine Wines International, Inc. dba Ethica Wines, of Miami, Florida
Kirkland Signature Valdobbiadene Prosecco DOCG bottlesThe Prosecco bottles can break or shatter, posing a laceration hazard.
- Class II
Medical Device Recall · November 6, 2025
BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm, Ureteral Stent Kit REF 788426Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
- Unclassified
Vehicle Recall · November 6, 2025
2023 NOVA BUS LFSA faulty indictor light, that cannot provide the driver with information about the status of the turn signals, increases the risk of a crash.
- Class II
Food Recall · November 6, 2025
Italian Salad Dressing; Net 1 GAL (3.78L) SKU: 7 67367 00518 4 Creamy Poblano Avocado Ranch Dressing and Dip; Net Contents 1 GAL93.78L) SKU: 7 34730 53243 1 Ventura Caesar Dressing; Net WT 2000LB (90foreign objects (black plastic planting material) in granulated onion
- Unclassified
Consumer Product Recall · November 6, 2025
Zhujisibeixuxinxizixunfuwubu dba Mengna, of China
Criblike aftermarket play yard and non-full sized crib mattressesThe aftermarket mattresses violate the mandatory standard for crib mattresses, as the mattresses may not adequately fit certain play yards or non-full-sized cribs, posing a deadly entrapment hazard. Babies can suffocate in gaps between an undersized mattress, or extra padding, and side walls of a product, especially when the infant's face becomes trapped against the side and the mattress, preventing the infant from breathing. The non-full-sized crib mattress also fails to meet the mandatory standard for mattress set flammability.
- Class I
Drug Recall · November 6, 2025
Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL vials, Rx only, Fresenius Kabi USA, LLC, NDC 63323-739-11 (unit of use), 63323-739-12 (unit of sale).Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
- Unclassified
Consumer Product Recall · November 6, 2025
STIHL Incorporated, of Virginia Beach, Virginia
STIHL BR 800 Backpack BlowerThe fan wheel inside the backpack blower can break apart, posing a laceration hazard.
- Unclassified
Consumer Product Recall · November 6, 2025
STARKIM KIMYA SAN.TIC. A.S, of Turkey
Y'all Can DIY Liquid Bioethanol Fireplace Fuel ContainersThe recalled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under the Portable Fuel Container Safety Act, posing a deadly risk of flash fire.
- Unclassified
Consumer Product Recall · November 6, 2025
Inkari B.V., of the Netherlands
Inkari Plush Alpaca ToysThe recalled toys are intended for children under three years of age and the eyes can detach, which violates the small parts ban, posing a choking hazard to children.
- Unclassified
Consumer Product Recall · November 6, 2025
Lezyne USA Inc., of San Luis Obispo, California
Lezyne Pressure Over Drive Bicycle Floor PumpsThe pump's canister can forcefully eject from the base when pressurized, posing a risk of serious injury from impact to the user or bystander.
- Unclassified
Consumer Product Recall · November 6, 2025
Vevor.com and Amazon.com from January 2025 through August 2025 for between $65 and $80.
Vevor Baby SwingsThe swings were marketed for infant sleep and have an incline angle greater than 10 degrees, violating the mandatory safety standard for Infant Sleep Products and the ban on inclined sleepers under the Safe Sleep for Babies Act, posing a deadly suffocation risk.
- Unclassified
Consumer Product Recall · November 6, 2025
Napei Collapsible Infant Bath TubsThe recalled infant bath tubs violate the mandatory standard for consumer products containing button cell or coin batteries because the built-in thermometer contains button cell batteries that can be accessed easily by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Unclassified
Consumer Product Recall · November 6, 2025
Konges Sløjd, of Copenhagen, Denmark
Three-Wheeled Children's Scooter with Foot BrakeThe left front wheel can detach during use, posing a fall hazard.
- Unclassified
Consumer Product Recall · November 6, 2025
Xindu District Miuwola Clothing Store dba Umeyda Company, of China
Umeyda NightgownsThe recalled nightgowns violate the mandatory flammability standards for children's sleepwear, posing a risk of burn injuries to children.
- Class II
Medical Device Recall · November 5, 2025
Brand Name: Diasol Product Name: 100230-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 litersSafety and efficacy of dialysis acid concentrate cannot be assured
- Class II
Medical Device Recall · November 5, 2025
Brand Name: Diasol Product Name: 100425-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 litersSafety and efficacy of dialysis acid concentrate cannot be assured
- Class II
Medical Device Recall · November 5, 2025
Brand Name: Diasol Product Name: 100225-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 litersSafety and efficacy of dialysis acid concentrate cannot be assured
- Class II
Medical Device Recall · November 5, 2025
Brand Name: Diasol Product Name: 100325-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 litersSafety and efficacy of dialysis acid concentrate cannot be assured
- Class II
Medical Device Recall · November 5, 2025
Brand Name: Diasol Product Name: 100220-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 litersSafety and efficacy of dialysis acid concentrate cannot be assured
- Class II
Medical Device Recall · November 5, 2025
Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE Whole Blood Microcoagulation SystemTest cuvettes, used with an assay for monitoring heparin anticoagulation, may have a foreign object that has sharp edges and could pose a risk of injury if not detected prior to handling.
- Class II
Food Recall · November 5, 2025
Prickly Pear Jelly. 9 oz (268 g) glass bottle with gold cap.Undeclared milk.
- Class II
Food Recall · November 5, 2025
Mama Rose's Prickly Pear Salad Dressing. 12 oz (340 g) glass bottle with gold cap.Undeclared sulfites.
- Class II
Medical Device Recall · November 5, 2025
Brand Name: Diasol Product Name: 100125-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 litersSafety and efficacy of dialysis acid concentrate cannot be assured
- Class II
Drug Recall · November 5, 2025
Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc., Naples, FL 34108, NDC 68180-353-09.Defective container - seal not adhering to bottles
- Class II
Food Recall · November 5, 2025
Laiwu Manhing Vegetables Fruits Co
Onion granules (irradiated) ; 55 lbs carton Item# 5358foreign objects (black plastic planting film) in granulated onion powder
- Class II
Medical Device Recall · November 5, 2025
Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10.Product testing did not meet expected stability criteria.
- Class I
Food Recall · November 5, 2025
Oven Dried Fish (SCOMBEROMORUS CAVALLA); distributed to walk-in customers of African Food on Wheels Inc. located at 1376 Randall Avenue, Bronx, NY 10474 only; Product is packed in a corrugated brown bClostridium botulinum (uneviscerated fish)
- Class II
Food Recall · November 5, 2025
Hollandia Dairy, Inc. 100% Appleberry Juice; Half Pint (236mL). UPC: 0 27495 03679 6100% Appleberry Juice contaminated with cleaning solution, Peracetic Acid.
- Class I
Food Recall · November 4, 2025
Sofit, Seedless Red Dates, 12 oz package, Plastic bags, 50 packages per caseUndeclared sulfites
- Unclassified
Vehicle Recall · November 4, 2025
2024 LINCOLN NAUTILUSA closing window may exert excessive force and pinch a driver or passenger before retracting, increasing the risk of injury.
- Unclassified
Vehicle Recall · November 4, 2025
2025 FORD EXPLORERA damaged park system can result in a vehicle rollaway when the vehicle is placed in park without the parking brake applied. An engine stall while driving can result in a sudden loss of drive power. Either of these scenarios can increase the risk of a crash.
- Unclassified
Vehicle Recall · November 4, 2025
2025 HYUNDAI IONIQ 5Reduced braking performance and unexpected, continued acceleration increase the risk of a crash.
- Class II
Medical Device Recall · November 4, 2025
Cardiosave Hybrid. Intra-Aortic Balloon Pump system.The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
- Class II
Food Recall · November 4, 2025
Tops Strawberry Jam INGREDIENTS: Sugar, Strawberry Pulp 30%, Gelling Agent (Pectin - INS 440), Acidity Regulator (Citric Acid - INS 330), Preservative (Sodium Benzoate - INS 211, Potassium MetabisulpUnapproved color (carmoisine).
- Class I
Food Recall · November 4, 2025
Organic Moringa Leaf Powder (Moringa Powder) , 4 oz. and 1 Kilogram, 4 oz size in a solid plastic container / 1 kg size in a plastic bag in a box. Distributed by: Africa Imports, South Hackensack, NJProduct tested positive for Salmonella.
- Class II
Medical Device Recall · November 4, 2025
Cardiosave Rescue. Intra-Aortic Balloon Pump system.The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
- Class II
Food Recall · November 4, 2025
Tops Mixed Fruit Jam INGREDIENTS: Sugar, Mixed Fruit Pulp 48% (Apple, Pear, Guava, Pineapple, Banana, Mango, Grapes, Papaya), Gelling Agent (Pectin - INS 440), Acidity Regulator (Citric Acid - INS 33Unapproved color (carmoisine).
- Class II
Medical Device Recall · November 3, 2025
Syphilis TestDistribution without premarket approval/clearance.
- Class III
Medical Device Recall · November 3, 2025
Brand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model/Catalog Number: 38-1007SP FORZA PTC Spacer, Straight, 0¿, 9W x 23L x 7H 38-1008SP FORZA PTC Spacer, Straight, 0¿, 9Labeling contains claims that are not consistently present.
- Class II
Medical Device Recall · November 3, 2025
Sperm TestDistribution without premarket approval/clearance.
- Unclassified
Vehicle Recall · November 3, 2025
2025 KEYSTONE KODIAKUnprotected electrical wiring can overheat and increase the risk of a fire.
- Class II
Medical Device Recall · November 3, 2025
Pollen Allergy TestDistribution without premarket approval/clearance.
- Unclassified
Vehicle Recall · November 3, 2025
2025 NISSAN SENTRAAn unsecured driver's seat may not adequately restrain the driver during a crash, increasing the risk of injury.
- Class II
Medical Device Recall · November 3, 2025
Diabetes Test (ketones & glucose)Distribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
NAD Profile TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Biological Age & Longevity TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
Blood Type TestDistribution without premarket approval/clearance.
- Class II
Medical Device Recall · November 3, 2025
3 in 1 STI TestDistribution without premarket approval/clearance.