Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 7,151–7,200 of 15,271
- Class II
Food Recall · April 12, 2025
Outer carton labeled: "Cookie Butter Banana Pie" Inner carton labeled: "Tropical Key Lime Pie" Product contained inside: "Cookie Butter Banana Pie" NET WT. 11 LB 2.8 OZ (5.06 kg) GROSS WT: 12.96 LB (Contains undeclared allergens (almonds).
- Class II
Food Recall · April 12, 2025
Multigrain Sourdough Freshly Backed, and Half Multigrain Sourdough Artisan Bread, 15 oz; 7 oz, Bag, 1 unitFirm is recalling product due to the potential of foreign material (glass)
- Class II
Food Recall · April 12, 2025
Ancient Grains Hoagie Roll, 4 oz, Paper carton (corrugated), CP45, FrozenGlass fragment found on top of bread.
- Class II
Food Recall · April 12, 2025
Whole Grain Multigrain , 20 oz, Paper carton (corrugated), CP12, FrozenGlass fragment found on top of bread.
- Unclassified
Vehicle Recall · April 12, 2025
2026 BMW X5, 2026 BMW X6, 2026 BMW X7An air bag that does not deploy properly can increase the risk of injury during a crash.
- Class II
Medical Device Recall · April 11, 2025
Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).
- Class I
Medical Device Recall · April 11, 2025
Nipro Renal Soultions USA, Corporation
MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in corrugated shipper cases (4 bottles per shipper case).Potential for the presence of visible foreign matter.
- Class I
Medical Device Recall · April 11, 2025
iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
- Class II
Medical Device Recall · April 11, 2025
TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34, 1651-38, 1651-44, 1651-48, 1651-58, 1651-64, 1651-68, 1651-78, 1651-84, 1651-88, E1651-34, E1651-38, E1651-44, E1651-48, E16During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).
- Class I
Medical Device Recall · April 11, 2025
Integra LifeSciences Corp. (NeuroSciences)
CODMAN Disposable Perforator, 14mm. Cranial perforator.Inadequate weld that can potentially cause the product to disassemble.
- Class II
Medical Device Recall · April 11, 2025
Pruitt Occlusion Catheter. Catalog Numbers: 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).
- Class II
Food Recall · April 11, 2025
Emily Kate's Gluten Free Vanilla Cake, Net Wt. 6.4oz, Emily Kate's Foods, Kansas City, KS 66106, UPC 850581007253Foreign material (foil) found in cake slices
- Class II
Food Recall · April 11, 2025
Emily Kate's Gluten Free Carrot Cake, Net Wt. 6.4oz, Emily Kate's Food, LLC, Kansas City, KS 66106, UPC 850581007284Foreign material (foil) found in cake slices
- Class I
Medical Device Recall · April 11, 2025
Centerline Biomedical IOPS Guidewire 2, REF ATW-2; Sensorized wire used to navigate through vasculature to facilitate placement of a catheterCenterline Biomedical has determined that the coating on the guidewires for lot 2404-2005 may delaminate during use of the guidewire.
- Class I
Medical Device Recall · April 11, 2025
Integra LifeSciences Corp. (NeuroSciences)
CODMAN Craniotomy Kit, Disposable Perforator Cranio-blade Wire Pass Drill, 14mm. Cranial perforator kit.Inadequate weld that can potentially cause the product to disassemble.
- Class I
Medical Device Recall · April 10, 2025
CADD-Solis Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS, MDL 2110, V4.2, CE ENGLISH 1/EA, Model Number: 21-2111-0402-51; 2) PUMP KIT, CADD-SOLIS, MDL 2110, V4.2, YELLOW, CE ENGLISH 1/There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
- Class II
Medical Device Recall · April 10, 2025
Contec Medical Systems Co., Ltd.
CMS8000 Patient MonitorPatient monitor has nine identified cybersecurity vulnerabilities.
- Class II
Medical Device Recall · April 10, 2025
Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder replacement.A software bug in Blueprint version 4.2.1 prevents users from accessing cases initiated in previous versions of the software.
- Unclassified
Consumer Product Recall · April 10, 2025
Jinjiangshiweixiaobaobeiyingtongyongpin Co.Ltd., dba Bebamour, of China
Bebamour baby bath seatsThe recalled bath seats violate the federal safety regulation for infant bath seats because the bath seat is unstable and can tip over while in use, and the leg openings are too wide, allowing a baby to slip out of the seat, posing a risk of serious injury or death to babies from drowning.
- Unclassified
Consumer Product Recall · April 10, 2025
Modus Furniture International, of Los Angeles, California
Kentfield Solid Wood Eight-Drawer DressersThe recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate performance requirements of the STURDY Act.
- Class I
Medical Device Recall · April 10, 2025
Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH265 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit Kit Dual-limb, Dual-hAdapters may disconnect during setup or while in use, potentially interrupting ventilation. Any disconnection can result in severe consequences for neonates, including hypoxia, hypercapnia, and organ failure.
- Class II
Drug Recall · April 10, 2025
Testosterone Cypionate Injection, USP, CIII, 200mg per mL, Rx only, 1mL Single-Dose Vial, Distributed by Eugia US LLC, E. Windsor, NJ, Manufactured by: Eugia Specialties Limited, Telangana State, IndcGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
- Class II
Food Recall · April 10, 2025
CPK TEQUILA LIME BASE ALLERGENS: MILK NET WEIGHT: 1 LB Case UPC FG15453558 Manufactured for California Pizza Kitchen, Inc.***Los Angeles, CAForeign Object - Wood. The firm was notified by their supplier that the product may contain pieces of wood.
- Unclassified
Consumer Product Recall · April 10, 2025
Costway, of Fontana, California
Babyjoy Convertible 6-in-1 High Chair Activity CentersThe recalled high chair activity centers violate the federal regulations for high chairs and stationary activity centers. The high chair activity centers pose a deadly entrapment hazard because the leg openings in the seat of the stationary activity center are too wide and a child can become entrapped in it, which is a violation of the federal regulation for stationary activity centers. In addition, the tray can disengage and a child can fall, which is a violation of the federal regulation for high chairs, posing a serious injury hazard.
- Class I
Medical Device Recall · April 10, 2025
CADD-Solis HPCA Ambulatory Infusion Pump; Model/Number: 21-2111-0402-09-KYO 21-2111-0402-09-KYO CADD SOLIS PIB PUMP FOR CLINICAL EVALUATION/DEMO PUMP 21-2111-0300-09_LOAN CADD SOLIS PIB PUMP FOR CLIAffected pumps may trigger an erroneous (false) Upstream Occlusion Alarm under certain conditions, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.
- Class I
Medical Device Recall · April 10, 2025
CADD-Solis VIP Ambulatory Infusion Pump; Model/Number: 21-2120-0100-02 21-2120-0100-03 21-2120-0100-06 21-2120-0100-232 21-2120-0100-233 21-2120-0100-50 21-2120-0100-51 21-2120-0100-95 21Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm under certain conditions, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.
- Class I
Medical Device Recall · April 10, 2025
3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370Field action to clarify the flow rates and inlet fluid temperatures, along with location of the outlet temperature for Ranger Blood/Fluid Warming High Flow Sets.
- Class I
Medical Device Recall · April 10, 2025
Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH165 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit dual-limb, dual-heat,Adapters may disconnect during setup or while in use, potentially interrupting ventilation. Any disconnection can result in severe consequences for neonates, including hypoxia, hypercapnia, and organ failure.
- Class II
Drug Recall · April 10, 2025
clomiPRAMINE hydrochloride Capsules USP, 25 mg, 100-count bottle, Rx only, Manufactured For: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, United States, Manufactured By: Lupin Limited, Nagpur, 44Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during 18-month long term stability study.
- Class I
Food Recall · April 10, 2025
MO-CHA brand Premium Non-Dairy Creamer; INGREDIENTS Glucose syrup, Refined vegetable oil, Whey powder, Sugar, Casein, Emulsifier (471, 481i), Stabilizer(340ii, 452i), Anti-caking agent(551), Food flavProduct does not declare the allergen, milk, on the label.
- Unclassified
Consumer Product Recall · April 10, 2025
Shandong ODES Industry Co. Ltd., of China
E-Bully Youth All-Terrain Vehicles (ATVs)The recalled youth ATVs fail to comply with the requirements of the federal mandatory ATV safety standard. The handlebars pose a laceration hazard if the child rider's body or head impacts the handlebars at a high rate of speed. Additionally, the parking brakes fail to hold, posing a collision hazard. ATVs that fail to meet the mandatory safety requirements pose a risk of serious injury or death.
- Class I
Medical Device Recall · April 10, 2025
CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL MODE, 1/EA, Model Number: 21-2127-0105-01; 2) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA EThere is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
- Class I
Medical Device Recall · April 10, 2025
CADD Solis HSPCA Pump ***Updated 5/27/26*** Scope updated to apply specifically to customers using the wireless system. Affected products associated with the change in scope: PUMP KIT, CADD SOLIS HPPumps may experience Wireless Connection Modules intermittent connection alarms, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.
- Unclassified
Consumer Product Recall · April 10, 2025
Fisher-Price Inc., of East Aurora, New York
Brunch & Go Stroller ToysThe yolk of the toy egg can crack and create small parts, posing a choking hazard to young children.
- Unclassified
Consumer Product Recall · April 10, 2025
Fisher-Price Inc., of East Aurora, New York
Tissue Box Toy sold with Fisher-Price 3-in-1 SnugaPuppy Activity CentersThe detachable tissue box toy can come apart, exposing the small support brackets, posing a choking hazard to young children.
- Unclassified
Consumer Product Recall · April 10, 2025
Cheng du shi ri teng mao yi you xian gong si, DBA Jonas C, of London, Ohio
Long-Haul 5L ATV Gas CansThe portable fuel containers violate the child-resistant requirements for closures under the Children's Gasoline Burn Prevention Act. The closure for the product is not child-resistant, posing a risk of burn, fire and poisoning to children and the risk of serious injury and death.
- Unclassified
Consumer Product Recall · April 10, 2025
Safetussin Max Strength Multi-Symptom Cough, Cold and Flu tablets blister packsThe Safetussin over-the-counter cold medicine contains acetaminophen, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The packaging of the products is not child-resistant as a tablet can be pushed through the foil, posing a risk of poisoning if the contents are swallowed by young children.
- Unclassified
Consumer Product Recall · April 10, 2025
Lucky Bird Inc., of Buffalo, New York
Multifunctional Puzzle Crab ToysThe recalled magnetic Multifunctional Puzzle Crab Toy set violates the mandatory federal regulation for magnet toys, posing an ingestion hazard. 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.
- Unclassified
Vehicle Recall · April 9, 2025
2023 JEEP GRAND CHEROKEE, 2024 JEEP GRAND CHEROKEE, 2025 JEEP GRAND CHEROKEE, 2026 JEEP GRAND CHEROKEEA loss of drive power increases the risk of a crash.
- Class II
Medical Device Recall · April 9, 2025
MEDLINE INDUSTRIES, LP - Northfield
Centurion Sterile Weitlaner Retractor, Reorder: 67315Three is the potential for the retractors to puncture through the sterile packaging.
- Class II
Medical Device Recall · April 9, 2025
MEDLINE INDUSTRIES, LP - Northfield
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395Three is the potential for the retractors to puncture through the sterile packaging.
- Class II
Medical Device Recall · April 9, 2025
FoundationOne Companion Diagnostic (F1CDx)Four (4) total reports were sent to customers with clinically relevant variants requiring amendment, one (1) of which with an incorrect negative CDx claim. The remaining three (3) with tumor profiling result changes did not impact CDx indications.
- Class II
Drug Recall · April 9, 2025
Wegovy (semaglutide) injection, 2.4 mg/0.75 mL, 4 Single-Dose Prefilled Pens per Carton, For Subcutaneous Use Only, Rx Only, Single-Dose Only, Novo Nordisk Inc., Plainsboro, NJ 08536, Manufactured by:Temperature abuse: Wegovy product was potentially exposed to temperatures outside of the products labeled storage conditions due to a shipping error involving a Cardinal Health distribution center. More specifically, product was removed from refrigerated storage for an extended period of time and inappropriately released.
- Unclassified
Vehicle Recall · April 9, 2025
2023 IC BUS CESB, 2025 IC BUS CESBReduced structural integrity may increase the risk of injury in a crash.