Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 6,601–6,650 of 15,271
- Class I
Food Recall · May 20, 2025
10lbs. Cucumbers Sliced 1/4", 5 lbs. Cucumber Sliced 1/4"Product is contaminated with Salmonella
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Classic Crab Roll Sushi Net Wt. 10.5oz UPC 0 23012 00702 7Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class II
Medical Device Recall · May 20, 2025
BD BACTEC MGIT 960 PZA Kit. IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA).BD has received additional complaints of intermittent false resistance results for PZA during susceptibility testing of Mycobacterium tuberculosis isolates.
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Hybrid Yon Tray 50pc Net Wt. 53.8oz UPC 0 23012 94261 8Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Crunchy CA Roll 10pc Net Wt 8.1oz UPC 0 23012 94283 0 & UPC 0 23012 95144 3Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Mango Red Rock 5pc Net Wt. 9.8oz UPC 0 23012 94497 1Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Spicy Roll - Shrimp 10pc Net Wt. 7.1oz UPC 0 23012 94316 5Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Crunchy Roll - Salmon 10pc Net Wt. 10.0oz UPC 0 23012 95040 8Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Yuzu Teriyaki Sauce 3oz Net Wt. 3oz UPC 0 23012 95076 7Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Hawaiian Roll 10pc Net Wt. 11.0oz UPC 0 23012 94363 9Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Crunchy Shrimp Tempura Roll 10pc (Brown Rice) Net Wt 9.1oz UPC 0 23012 94290 8Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Hybrid Roku Tray 82pc Net Wt. 88.6oz UPC 0 23012 94259 5Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Premium Chef Sampler #1 (Rainbow, Salmon, Dragon, Dynamite) 20pc Net Wt. 19.9oz UPC 0 23012 94302 8Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class I
Food Recall · May 20, 2025
ZENSHI HANDCRAFTED SUSHI Hawaiian Roll - Salmon, Tuna 10pc Net Wt. 10.6oz UPC 0 23012 94364 6Salmonella. The firm received cucumbers which were recalled due to possible Salmonella. The cucumbers were used to make Sushi.
- Class II
Medical Device Recall · May 19, 2025
Neurovision Medical Products Inc
Brand Name: Hummingbird Product Name: Stimulated EMG Kit with Hummingbird - Model/Catalog Number: REF I-D-BMF90, 1 Single-Use Bipolar Minifork Stimulation Probe, 90mm, and 1 Green Ground Needle ;Product packaging contains the wrong part number and kit contents.
- Class II
Medical Device Recall · May 19, 2025
PRIMA 2MM ECCENTRICAL ADAPTOR WITH SCREW REF: 1367.15.702, SterileThere is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing.
- Class III
Drug Recall · May 19, 2025
Glenmark Pharmaceuticals Inc., USA
Ezetimibe and Simvastatin Tablets, 10mg/40mg, 90-count bottle, Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd., Plot No. 2, Phase-2, Pharma Zone SEZ, Madya Pradesh, India, Manufactured for: GlFailed Impurities/Degradation Specifications: Out of Specification (OOS) for related substances test for Anhydro Simvastatin at the 06-month time point during long-term stability study.
- Class I
Food Recall · May 19, 2025
NON FAT DRY MILK. "LOW HEAT SPRAY PROCESS GRADE A NON FAT DRY MILK MADE FROM PASTERUIZED MILK, NET WEIGHT 25.00 KG, PRODUCT OF U.S.A."Potential contamination with Salmonella.
- Class II
Medical Device Recall · May 19, 2025
PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, SterileThere is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing.
- Class II
Medical Device Recall · May 16, 2025
Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit Model/Catalog Number: CLXUSA Software Version: Not Applicable Product Description: THERAKOS Photopheresis or extracorIncreased difficulty in installing the centrifuge bowl onto the centrifuge bowl holder. Improper installation may cause the centrifuge bowl to dislodge, resulting in a broken bowl during the prime cycle or treatment phase, leading to a delay in patient treatment and blood loss.
- Class II
Medical Device Recall · May 16, 2025
GE Medical Systems China Co., Ltd.
GE Healthcare LOGIQ F R3 Ultrasound System, Model/Catalog Number 5943263, diagnostic ultrasound systemGE HealthCare has become aware that the Estimated Fetal Weight (EFW) measurement data feature on the Versana Premier R3 and LOGIQ F R3 series ultrasound systems can display previous obstetric patient data in the Whizz report. This could potentially lead to an incorrect clinical decision due to inaccuracy in the fetal size and growth calculation.
- Class II
Medical Device Recall · May 16, 2025
GE Medical Systems China Co., Ltd.
GE Healthcare Versana Ultrasound Systems, sold under the following names and Model/Catalog Numbers: 1) Versana Premier R3 VS, Model/Catalog Number 5938558; 2) Versana Premier R3 VA, Model/CatalogGE HealthCare has become aware that the Estimated Fetal Weight (EFW) measurement data feature on the Versana Premier R3 and LOGIQ F R3 series ultrasound systems can display previous obstetric patient data in the Whizz report. This could potentially lead to an incorrect clinical decision due to inaccuracy in the fetal size and growth calculation.
- Class I
Food Recall · May 16, 2025
Cucumbers, Wholesale Produce Supply, Bedner Growers, Inc. 10066 Lee Road Boynton Beach, FL 33473 (561)733-5490. Cucumbers were packaged in cardboard shipping boxes to customers with packaging sizes coCucumbers may be potentially contaminated with Salmonella
- Class II
Food Recall · May 16, 2025
Madeline's Patisserie 4.25 Inch Butter Croissant Bun, Net Wt. 4 lbs. 6 oz (1,984.47 g), packaged in a food safe polypropylene bag and packed in a food service case; 24 per caseUndeclared wheat
- Class I
- Class II
Drug Recall · May 15, 2025
Glenmark Pharmaceuticals Inc., USA
Theophylline (Anhydrous) Extended-Release Tablets, 600 mg, 100 Tablets per bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited. Colvale-Bardez, Goa - 403513, India. Manufactured for: GlOOS results reported for the Dissolution (by UV) test.
- Class II
Medical Device Recall · May 15, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250There is a possible packaging defect impacting the outer Tyvec pouch that protects the sterile product.
- Class I
Medical Device Recall · May 15, 2025
Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic and therapeutic procedures. Catheters are available in various configurations. Configurations include different shaft lenCook Medical identified that catheters supplied in the affected device lots may experience tip separation.
- Class II
Medical Device Recall · May 15, 2025
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solutionContact lens insertion solution may lack sterility.
- Unclassified
Consumer Product Recall · May 15, 2025
Polaris Industries Inc., of Medina, Minnesota
Model Year 2023-2025 Ranger XP 1000 NorthStar and Ranger XP 1000 NorthStar Crew Recreational Off-Road Vehicles (ROVs)The lower seat belt anchor fasteners were not properly tightened, which can result in the seat belt separating from the vehicle frame, failing to protect riders. Without that protection, riders can be ejected from the vehicle in a crash, posing an injury hazard.
- Class II
Medical Device Recall · May 15, 2025
Siemens Medical Solutions USA, Inc
interventional fluoroscopic x-ray systemIn very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose.
- Class II
Medical Device Recall · May 15, 2025
Siemens Medical Solutions USA, Inc
ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. ProcIn very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose.
- Class II
Medical Device Recall · May 15, 2025
Siemens Medical Solutions USA, Inc
interventional fluoroscopic x-ray systemIn very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose.
- Class II
Medical Device Recall · May 15, 2025
Siemens Medical Solutions USA, Inc
interventional fluoroscopic x-ray systemIn very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose.
- Class II
Drug Recall · May 15, 2025
BD ChloraPrep Clear, 2% x/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), Patient Preoperative Skin Preparation, Sterile Solution, Applicator is sterile if package is intact, FlamLack of Assurance of Sterility: The affected product may exhibit an open seal on the packaging of the applicator.
- Unclassified
Consumer Product Recall · May 15, 2025
Boyro Baby Convertible High ChairsThe high chairs pose a deadly fall hazard to babies because the restraint system is not attached to the product and the locks or latches can fail. In addition, the high chairs pose an entrapment hazard because the opening between the seat and tray is large enough that a child can become entrapped in it. These are violations of the federal regulations for high chairs.
- Unclassified
Consumer Product Recall · May 15, 2025
Fat Brain Toy Co. LLC, of Elkhorn, Nebraska
PlayTab Rollers Tile ToysThe recalled rollers tile toy violates the mandatory federal regulation for toy magnets because it contains a magnet that can become loose, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, infection, blood poisoning, and death.
- Unclassified
Consumer Product Recall · May 15, 2025
Yiwu Baili Import and Export Co., of China
Child Safety GatesThe recalled child safety gates violate the federal safety regulation for expansion gates and expandable enclosures because a child's torso can fit through the opening between the gate slat and side wall, a child's torso can fit through the secondary opening, the locking mechanism does not fully engage and/or the gate does not resist a push-out force. These failures pose a risk of serious injury or death due to entrapment and fall hazards.
- Unclassified
Consumer Product Recall · May 15, 2025
FidgetThings, of Las Vegas, Nevada
Chill Pill Magnetic Haptic Fidget Toys Red BumpyThe recalled magnetic fidget pill toy violates the mandatory federal regulation for magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or another metal object, and become lodged in the digestive system. This can result in perforations, twisting and/or blockage of the intestines, infection, blood poisoning and death.
- Class I
Medical Device Recall · May 15, 2025
Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36-23446 Rev 2 Print Version The Broselow Tape is a length- and weight-based reThe impacted tape was manufactured with incorrect information on the tape. Incorrect values are printed in the Red zone, Orange zone, and Grey zone. Using the incorrect values in the Red zone could lead to shocking a patient with an excessive dose of joules, causing significant harm including burns, heart damage, and cardiac arrest. Incorrect values in the Orange zone could lead to overdosing the patient with sodium bicarbonate and cause metabolic alkalosis, electrolyte imbalances, tissue damage, and worsen respiratory status. Incorrect information in the Grey may lead to underdosing the patient with sodium bicarbonate and may cause reduced myocardial contractility, decreased response to vasopressors, and increased risk of dysrhythmia.
- Unclassified
Consumer Product Recall · May 15, 2025
Children's Mini Danica Loungewear SetsThe recalled children's pajama sets violate flammability standards for children's sleepwear, posing a burn hazard and risk of serious injuries or death to children.
- Unclassified
Consumer Product Recall · May 15, 2025
GASGAS and Husqvarna Off-Road MotorcyclesThe front brake caliper can crack, reducing the braking system's effectiveness, posing a crash hazard.
- Unclassified
Consumer Product Recall · May 15, 2025
Nicrew Technology Co. Limited, of China
NICREW 15" Submersible RGB LED Lights with remote controlsThe Submersible RGB LED Light's remote control has a lithium coin battery that can be easily accessed by children, posing an ingestion hazard. This violates the mandatory federal regulations for consumer products containing button cell or coin batteries. In addition, the recalled products do not have the required warnings. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Unclassified
Consumer Product Recall · May 15, 2025
Leon Rading Co. Ltd., of Owatonna, Minnesota
Digital Wall ClocksThe recalled digital wall clocks violate the mandatory federal regulations for consumer products containing button cell or coin batteries. The remote control for the clock has a lithium coin battery that can be easily accessed by children, posing an ingestion hazard. In addition, the recalled products do not have the warnings 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 · May 15, 2025
Shanghai Kai Rong Xin Xi Ke Ji Co. Ltd., of China
LivingCaring Adult Portable Bed RailsThe recalled bed rails violate federal regulations for adult portable bed rails, posing a serious entrapment hazard and risk of death by asphyxiation. When the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress. In addition, the bed rails do not bear the required hazard warning labels.
- Class I
Medical Device Recall · May 14, 2025
Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog Number: FEMII016A Software Version: N/A Product Description: The Edwards FEMFLEXII Femoral Perfusion Cannluae providesdue to complaints received for 3mm to 4mm section wire exposed/protruding from the outside of the cannula body.