Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 5,851–5,900 of 15,271
- Class II
Food Recall · June 27, 2025
Cool Watermelon Bar (86270), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a masterPotential Listeria Monocytogenes Contamination
- Class II
Medical Device Recall · June 27, 2025
Injection needle, bayonet, Luer-Lock, 1. Model no. 50-353-23, working length 25 cm, total length 31cm, nonsterile; 2. Model no. 50-345-23, working length 24 cm, total length 31 cm, non-sterileAffected product show elevated cytotoxicity values. Use of affected injection needles may present a risk of intolerance reaction or allergic reaction.
- Class II
Food Recall · June 27, 2025
Orange Cream Bar (86010), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master caPotential Listeria Monocytogenes Contamination
- Class II
Medical Device Recall · June 27, 2025
Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.Device does not comply with the labeling requirements of international standard IEC 60601-1.
- Class III
Food Recall · June 27, 2025
Cajeta cupcakes (Box). Vanilla cake decorated with suspiros cream and dulce de leche-milk caramel filling. Blister plastic tray with lid (Box). Box: 6 servings (438 gr). Box: SKU89Multiple cake products contain goat milk, which was labeled as "milk"
- Class II
Food Recall · June 27, 2025
Savagely Sour BlueRasberry Bar (86265), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 unitsPotential Listeria Monocytogenes Contamination
- Class II
Food Recall · June 27, 2025
Rich Bar (85155), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep FPotential Listeria Monocytogenes Contamination
- Class II
Food Recall · June 27, 2025
Cotton Candy Twirl Bar (86260), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a masPotential Listeria Monocytogenes Contamination
- Class III
Food Recall · June 27, 2025
Suspiros Cajeta Cake. 15 P: 20 servings (2000 gr), 4P: 4.8 servings (480gr). UPC= 15P: 1338, 4P: 6965. Type of packaging: Plastic dome and plate (15P and 4P). Firm name: NOVACAB SAPI de CV. Address liMultiple cake products contain goat milk, which was labeled as "milk"
- Class II
Food Recall · June 27, 2025
Strawberry Shortcake Bar (85050), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a masPotential Listeria Monocytogenes Contamination
- Class II
Food Recall · June 27, 2025
Crumbled Cookie Bar (85200), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master cPotential Listeria Monocytogenes Contamination
- Class II
Food Recall · June 27, 2025
Chocolate Crunch Cake Bar (85000), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a maPotential Listeria Monocytogenes Contamination
- Class III
Food Recall · June 27, 2025
Suspiros 4 Leches Cake. 15 P: 26 servings (2600 gr), 4P: 7 servings (700 gr), Pocket: 4.1 servings (410gr). UPC=15P: 1343, 4P: 6969, POCKET: 7904. Type of packaging: Plastic dome and plate (15P and 4Multiple cake products contain goat milk, which was labeled as "milk"
- Class III
Food Recall · June 27, 2025
Suspiros Choconut Cake. 15 P: 36.7 servings (2018 gr), 4P: 9.9 servings (544 gr). UPC= 15P: 1300, 4P: 698. Type of packaging: Plastic dome and plate (15P and 4P). Firm name: NOVACAB SAPI de CV. AddreMultiple cake products contain goat milk, which was labeled as "milk"
- Class I
Drug Recall · June 27, 2025
Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Manufactured in Austria by Sandoz GmbH for Sandoz Inc. Princeton, NJ 08540, NDC: 0Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled as penicillin G potassium for Injection, USP, 20 million Unit
- Class III
Food Recall · June 27, 2025
Suspiros Mazapan Cake. 15 P: 36 servings (1980gr). 4P: 9.5 servings (522gr). UPC= 15P: 1296 4P: 6975. Type of packaging: Plastic dome and plate (15P and 4P). Firm name: NOVACAB SAPI de CV. Address liMultiple cake products contain goat milk, which was labeled as "milk"
- Class II
Food Recall · June 27, 2025
Savagely Sour Cherry Bar (86266), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a mPotential Listeria Monocytogenes Contamination
- Class III
Food Recall · June 27, 2025
Suspiros Cheese Cake Coyota. 15 P: 15 servings (1875gr). UPC=7443. Type of packaging: Plastic dome and plate. Firm name: NOVACAB SAPI de CV. Address listed on label: El paso, TX 79901, USA.Multiple cake products contain goat milk, which was labeled as "milk"
- Class II
Food Recall · June 27, 2025
Fudge Frenzy Bar (86210), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master caPotential Listeria Monocytogenes Contamination
- Class III
Food Recall · June 27, 2025
Suspiros Chocoflan Cake.15 P: 13.7 servings (1712 gr). UPC=177. Type of packaging: Plastic dome and plate. Firm name: NOVACAB SAPI de CV. Address listed on label: El paso, TX 79901, USA.Multiple cake products contain goat milk, which was labeled as "milk"
- Class II
Medical Device Recall · June 27, 2025
LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894K (6-pack), 2) REF 0894P (2-pack)KWIK-STIK REF numbers: 0894P, 0894K and LYFO DISK" 0894L may result in failure to recover the target microorganism. All lots of REF 894-76 are impacted.
- Class III
Drug Recall · June 26, 2025
Pitavastatin Tablets, 1 mg, 90 Tablets per bottle, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC: 42291-905-90Failed Impurity/Degradation Specifications
- Class III
Drug Recall · June 26, 2025
Pitavastatin Tablets, 2 mg, 90 Tablets per bottle, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC: 42291-906-90Failed Impurity/Degradation Specifications
- Unclassified
Consumer Product Recall · June 26, 2025
Ningbo New Team Import & Export Co. Ltd. ("Lera"), of China
DR Power LiPRO rechargeable lithium-ion battery packs (5.0 Ah)The recalled battery packs can short-circuit and ignite, posing fire and burn hazards to consumers.
- Class II
Medical Device Recall · June 26, 2025
UIBC (Unsaturated Iron Binding Capacity), REF: OSR61205,Beckman Coulter identified that the Unsaturated Iron Binding Capacity (UIBC) assay is not meeting their labeled hemoglobin interference claims of no significant interference (i.e., less than 10%) up to 200 mg/dL hemoglobin as indicated in their instructions for use. Initial internal testing confirmed that samples with low UIBC levels failed the claimed hemolysis interference specifications with reported biases up to -43.6 % UIBC when hemolyzed serum samples contained 200 mg/dL hemoglobin.
- Class II
Food Recall · June 26, 2025
Wei-Chuan branded Black Fungus Slice. Net weight: 2.5 oz UPC#: 072869231321"Wood-Ear" mushroom tested positive for Salmonella.
- Class II
Medical Device Recall · June 26, 2025
Siemens Healthcare Diagnostics Inc
RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number: 10329097.Siemens Healthcare Diagnostics is recalling the RAPIDPoint 500 Systems Wash/Waste Cartridge Lot WW/08925 due to a manufacturing error causing positive and negative bias in Ionized Calcium, Potassium, pH, Chloride, pCO2, Glucose and Lactate analytes and their derivatives. Four complaints were filed related to this event that led to Siemens Healthcare Diagnostics identifying an error in the manufacturing process and initiated corrective actions. Use of the affected device may result in errors during QC which could lead to a delay in patient treatment. If bias generated from this issue is not caught during QC erroneous results may cause temporary or medically reversible adverse health consequences to patients.
- Unclassified
Consumer Product Recall · June 26, 2025
Newell Brands Inc., an affiliate of The Coleman Company, Inc., of Atlanta, Georgia
Converta camping cots and Converta camping suspension stretchersThe backrest fold mechanism can pinch consumers' fingers, posing laceration and amputation hazards.
- Unclassified
Consumer Product Recall · June 26, 2025
Bell Sports Inc., of Irvine, California
Bell Sports Bicycle HelmetsThe recalled helmets do not comply with the impact requirements of the Consumer Product Safety Commission's (CPSC) mandatory federal safety standard for bicycle helmets. The helmets can fail to protect the user in the event of a crash, posing a risk of head injury.
- Unclassified
Consumer Product Recall · June 26, 2025
iHerb LLC, dba Madre Labs LLC, of Irvine, California
California Gold Nutrition Iron Supplements: Daily Prenatal Multi, Ultamins Women's Multivitamin, and Ultamins Women's 50+ MultivitaminThe recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The iron-containing dietary supplement packages violate the federal standard for child-resistant packaging because the bottles and blister packs are not child-resistant, posing a risk of deadly poisoning, if the contents are swallowed by young children.
- Unclassified
Consumer Product Recall · June 26, 2025
Sanven Technology Ltd., dba Vevor, of Rancho Cucamonga, California
Vevor Single Post HandrailsThe handrails' welding can break while a consumer is holding onto the handrail when stepping down a flight of stairs, posing an injury hazard.
- Unclassified
Consumer Product Recall · June 26, 2025
Total Saddle Fit, LLC, of Jamul, California
Shoulder Relief Saddle CinchesThe cinch can come apart and cause the saddle to fall off, posing fall and injury hazards to the rider.
- Class I
Medical Device Recall · June 26, 2025
Breathing circuit set, coaxial, 1.80 m, with flow sensor and expiratory valve set, REF: 260128, used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1 ventilators.Ventilator coaxial breathing circuit may have a crack in blue tubing, which is used to deliver fresh gas to the patient. The crack will compromise inspiratory and expiratory flows, leading to partial or complete rebreathing of exhaled gases, which could lead to acute hypercapnia, respiratory acidosis, and if unrecognized organ dysfunction.
- Class II
Medical Device Recall · June 26, 2025
VITEK¿ 2 Gram-negative AST Test Kits (Cards) containing Colistin formulation cs02n. VITEK¿ 2 is an automated system consisting of instruments, software and reagent cards designed for the identificaPotential for false resistant results for Colistin (cs02n) with multi-drug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii complex used in specific cards
- Unclassified
Consumer Product Recall · June 26, 2025
Hangzhou Christine Trading Co. Ltd., dba Boyro Baby, of China
Boyro Baby WalkersThe recalled baby walkers violate the federal safety standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step as required, posing a risk of serious injury or death due to a fall hazard. In addition, the baby walkers' brake pads contain levels of lead that exceed the federal lead content ban that are prohibited in children's products by the Federal Hazardous Substances Act. Lead is toxic if ingested by young children and can cause adverse health effects.
- Unclassified
Consumer Product Recall · June 26, 2025
Green Pastures Wholesale, of Baltimore, Maryland
LED Fireplace LanternsThe recalled lanterns violate the mandatory federal standard for consumer products containing button cell or coin batteries because the lithium coin battery in the remote control can be accessed easily by children, posing an ingestion hazard. In addition, the recalled products do not have the warning labels required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Unclassified
Consumer Product Recall · June 26, 2025
Peg Perego Tatamia 3-in-1 Recliner, Swings and High ChairsThe 3-in-1 products pose a suffocation risk because they were marketed for infant sleep, and they have an incline angle greater than 10 degrees, in violation of the Infant Sleep Products Rule and Safe Sleep for Babies Act. In addition, the products fail to meet mandatory warning requirements under the high chair standard.
- Unclassified
Consumer Product Recall · June 26, 2025
Professional's Choice Sports Medicine Products Inc., of Oklahoma City, Oklahoma
Swivel Port equine bits from Bob Avila collectionThe bit can break during use, posing a fall hazard to a rider.
- Class II
Food Recall · June 25, 2025
C Sweet Ghouribeh Rolls with date, sesame, & pistachios 10 oz., UPC 642896991132Undeclared wheat, soy, and sesame
- Class II
Food Recall · June 25, 2025
C Sweet Maamoul with Pistachios 8 oz., UPC 721782348967Undeclared soy, contains statement is present but does not list pistachios
- Class II
Medical Device Recall · June 25, 2025
DASH SARS-CoV-2 & Flu A/B Test Model/Catalog Number: SG-0006 combination COVID-19 and Flu test. Each DASH SARS-CoV-2 & Flu A/B Test is individually pouched and labeled. The tests are provideDue to manufacturing error, assay test may result in missed diagnosis or delay of treatment. (Potential false negative result)
- Class II
Medical Device Recall · June 25, 2025
UniCel DxI 600 Access Immunoassay Analyzer, Part Number A30260Beckman Coulter has identified that the UniCel DxI 600/800 systems with linear slide PnP gantries running software versions 5.7 and up faced incorrect PnP X-motor current settings where the PnP X-motor current incorrectly resets to 1.5A (instead of the required 2.0A) because the software overwrites the factory setting during installs or upgrades. This anomaly causes increased PnP motion errors which could lead to delays in reporting patient sample results if unnoticed.
- Class II
Food Recall · June 25, 2025
C Sweet Ghouribeh with Pistachios 7 oz., UPC 852664042755Undeclared soy, contains statement is present but does not list pistachios
- Class I
Food Recall · June 25, 2025
Front Panel: Danshi branded Shredded Tofu, 200g Rear Panel: Best before: 05/24/2025, Imported by: Shang Hao Jia, Inc. Address: South El Monte, CA 91733. Product of China. Manufacturer: Sichuan ShifaProduct does not declare allergen ingredient sesame.
- Class II
Medical Device Recall · June 25, 2025
UniCel DxI 800 Access Immunoassay Analyzer, Part Number 973100Beckman Coulter has identified that the UniCel DxI 600/800 systems with linear slide PnP gantries running software versions 5.7 and up faced incorrect PnP X-motor current settings where the PnP X-motor current incorrectly resets to 1.5A (instead of the required 2.0A) because the software overwrites the factory setting during installs or upgrades. This anomaly causes increased PnP motion errors which could lead to delays in reporting patient sample results if unnoticed.
- Class II
- Class II
Food Recall · June 25, 2025
C Sweet Maamoul with Dates 8 oz., UPC 852664042694Undeclared soy and wheat
- Class II
Medical Device Recall · June 25, 2025
MicroScan Neg MIC 3J REF C54814Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics
- Class II
Medical Device Recall · June 25, 2025
DxI 800 Access Immunoassay Analyzer W/Spot B, Part Number A71456Beckman Coulter has identified that the UniCel DxI 600/800 systems with linear slide PnP gantries running software versions 5.7 and up faced incorrect PnP X-motor current settings where the PnP X-motor current incorrectly resets to 1.5A (instead of the required 2.0A) because the software overwrites the factory setting during installs or upgrades. This anomaly causes increased PnP motion errors which could lead to delays in reporting patient sample results if unnoticed.
- Class II
Medical Device Recall · June 25, 2025
DxI 800 Access Immunoassay Analyzer W/Dual Gantry, Part Number A71457Beckman Coulter has identified that the UniCel DxI 600/800 systems with linear slide PnP gantries running software versions 5.7 and up faced incorrect PnP X-motor current settings where the PnP X-motor current incorrectly resets to 1.5A (instead of the required 2.0A) because the software overwrites the factory setting during installs or upgrades. This anomaly causes increased PnP motion errors which could lead to delays in reporting patient sample results if unnoticed.