Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 7,201–7,250 of 15,271
- Unclassified
Vehicle Recall · April 9, 2025
Toyota Motor Engineering & Manufacturing
2023 SUBARU Solterra, 2023 TOYOTA BZ4X, 2024 SUBARU Solterra, 2024 TOYOTA BZ4X, 2025 SUBARU SOLTERRA, 2025 TOYOTA BZ4XAn inoperative defroster and defogger system can decrease the driver's visibility under certain driving conditions, increasing the risk of a crash.
- Unclassified
Vehicle Recall · April 9, 2025
2025 CHRYSLER PACIFICAAn air bag with insufficient pressure retention increases the risk of ejection and injury during a crash.
- Unclassified
Vehicle Recall · April 9, 2025
2025 CRUISER AVENIRA damaged tire may blowout, increasing the risk of a crash.
- Unclassified
Vehicle Recall · April 9, 2025
2024 DODGE CHARGER EV, 2024 JEEP WAGONEER S, 2025 DODGE CHARGER EV, 2025 JEEP WAGONEER SA vehicle rollaway increases the risk of a crash.
- Unclassified
Vehicle Recall · April 9, 2025
2025 JEEP WAGONEER SAn incorrect cross beam may not adequately protect occupants in a crash, increasing the risk of injury.
- Class II
Medical Device Recall · April 9, 2025
PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric shockwaves (Therapeutic massager).The high voltage capacitor may fail early in the product life cycle after delivery of surge voltages. When this failure occurs, the capacitor may produce smoke and a burning smell. In extremely rare instances a capacitor may cause a spark or excessive heat when an internal capacitor failure occurs.
- Class II
Medical Device Recall · April 8, 2025
Artix MT Thrombectomy Device, REF: 32-102Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the radial force on the artery, which has the potential of vascular complications.
- Class II
Food Recall · April 8, 2025
GoodSource Solutions, Incorporated
Sauce, Creamy Butter; packaged in clear, unlabeled bulk 6-pound bags/4 bags to a case. Lot code# 701493 stamped on bag.Firm's product, Creamy Butter Sauce, was manufactured with recalled ingredient (Cilantro) which contained small wood like pieces.
- Class II
Medical Device Recall · April 8, 2025
REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164; C44703; C57017; C69412; C69413; C73942; C73941; C88470; C88471 The Normand InfoDue to a software issue, the software may incorrectly process the date of birth (DoB) received from the Laboratory Information System (LIS) and when the DoB is set to 01/01/1900 or left empty, REMISOL Advance may incorrectly identify a patient as a newborn, affecting the execution of validation rules based on incorrect reference ranges. The test results are not changed by this software defect and are accurately displayed by REMISOL Advance; however, the evaluation flagging of the results may be affected. This issue may lead to wrong reference range calculations and can result in erroneous flagged results being auto validated and uploaded to LIS.
- Unclassified
Vehicle Recall · April 8, 2025
2024 WINNEBAGO EKKO, 2025 WINNEBAGO EKKOOverloading may cause the outer tire to fail, increasing the risk of a crash.
- Class II
Medical Device Recall · April 7, 2025
Bio 1 Granules for Filling ¿ 1 mm (2 cm¿), REF:P822692243, Material: BIOSORB (BTCP 95% minimum purity)Vials of implant bone granules may contain less product then specified on labeling.
- Class I
Medical Device Recall · April 7, 2025
Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.A cybersecurity vulnerability was discovered through internal testing.
- Class II
Medical Device Recall · April 7, 2025
Molding Equipment. WCM series. Model WCM-330GL-iApic Yamada has recently discovered that certain products may be out of compliance with FDA electronic product regulations in that they did not bear a required label.
- Class II
Medical Device Recall · April 7, 2025
Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000USIncorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back label, shipping box and product inside correctly states 5.6/2.8.
- Class II
Medical Device Recall · April 7, 2025
Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line STerm , Adt/Pedi Intub CO2 Line STerm Lng , Adt/Pedi Intub CO2 Line High Humidity , Adt/Pedi Intub CO2Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.
- Class II
Medical Device Recall · April 7, 2025
Philips Medical Systems Nederland B.V.
IntelliSpace Cardiovascular software versions 6.x, 7.x, and 8.x; Model Number: 830089.An issue was identified with the software when using the Echo Module of ISCV, the issue may result in missing or incomplete information in the report.
- Class I
Medical Device Recall · April 7, 2025
Welch Allyn Life2000 Ventilation system, Product Codes: 1) BT-20-0002; 2) BT-20-0002A; 3) BT-20-0002AP; 4) BT200007; 5) BT-20-0007; 6) BT200011; 7) BT-20-0011; 8) RMS010118CP.A cybersecurity vulnerability was discovered through internal testing.
- Unclassified
Vehicle Recall · April 6, 2025
2025 NISSAN FRONTIER, 2025 NISSAN KICKSA rearview image that does not display can reduce the driver's view of what is behind the vehicle, increasing the risk of a crash.
- Unclassified
Vehicle Recall · April 6, 2025
Mazda North American Operations
2024 MAZDA MX-5, 2025 MAZDA MX-5An indicator light that does not illuminate may fail to warn the driver of a TCS or DSC system issue, increasing the risk of a crash.
- Class I
Food Recall · April 5, 2025
Heinen's Honey Roasted Peanuts, NET WT 8.25 OZ (234g), packaged in a composite can with plastic lid, 12 cans per case, Best If Used By: 10/01/2025 and Best By: 10/03/2025, UPC: 020601401877, DistributProduct mislabeled - product labeled as peanuts, but may contain cashews
- Class II
Food Recall · April 4, 2025
Moroccan Style Lentil Soup, 4 x 8lb pouches, Net wt. 32lbPotential contamination with foreign material (wood)
- Class II
Food Recall · April 4, 2025
Giant, Instant Oatmeal Raisins and Spice, 10 -1.5 oz. Packets, per box. Net. Wt. 15.01 oz.Undeclared Allergen (walnuts), was not on outer packaging but was on the inner packaging of product.
- Class II
Food Recall · April 4, 2025
Beecher's Street Corn, 18oz, 8 retail units per case, UPC 782045 115009Potential contamination with foreign material (wood)
- Class II
Medical Device Recall · April 4, 2025
Olympus Corporation of the Americas
Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser System Model/Catalog Numbers: TFL-SLS, TFL-PLS Product Description: SOLTIVE Laser Systems use technology toPreset treatment parameters are not consistently being used in accordance with the IFU.
- Class II
Food Recall · April 4, 2025
Mexican Street Corn Soup, 4 / 4lb pouches, Net Wt. 16lbPotential contamination with foreign material (wood)
- Class II
Food Recall · April 4, 2025
All American Trading Of Houston, Inc.
Texas Olive Company Capers Capote 8 oz. plastic containers. All lots with expiry prior to 06/04/2025 Texas Olive Company Capers Capote 16 oz. glass jar. All lots with expiry prior to 12/21/2025The recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed.
- Class II
Medical Device Recall · April 4, 2025
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:MXU-RV35 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates a self-contaPotential for internal fastening mechanism within generator of mobile x-Ray to fail.
- Class II
Medical Device Recall · April 4, 2025
Integra LifeSciences Corp. (NeuroSciences)
INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
- Class I
Food Recall · April 4, 2025
Marketside brand celery stick. Net wt. 1.6 OZ. (45g); Rear panel: 1 serving per container; Distributed by Wal-Mart Stores, Inc. Bentonville, AR 72716 UPC# 6 81131 16151 0Product tested positive for Listeria Monocytogenes.
- Class II
Medical Device Recall · April 4, 2025
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71, MXU-RV35 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates aPotential for internal fastening mechanism within generator of mobile x-Ray to fail.
- Class II
Food Recall · April 4, 2025
The Hot Chocolatier - St. Elmo, LLC
Blueberry Lemon Scones, bulk packaged in bakery boxes. Products are sold at retail in pastry cases and not individually labeled.Undeclared allergen (soy)
- Class II
Food Recall · April 4, 2025
All American Trading Of Houston, Inc.
Texas Olive Co. Pepperoncini 16 oz glass jarsThe recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed.
- Class I
Food Recall · April 4, 2025
Supplement Manufacturing Partner Inc.
Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules, oral consumption, shelf life: 24 months, PETE/White/150cc Plastic bottle/lid, 120 count.SuppleUndeclared allergen: Wheat
- Class II
Food Recall · April 4, 2025
All American Trading Of Houston, Inc.
Texas Olive Company Giardiniera 16 oz. glass jars All lots with expiry prior to 06/14/2025The recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed.
- Class II
Medical Device Recall · April 4, 2025
KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization ofPotential for microbial contamination.
- Class II
Food Recall · April 4, 2025
Cuban-Style Black Bean Soup, 4 / 4lb pouches, Net Wt. 16lbPotential contamination with foreign material (wood)
- Class II
Medical Device Recall · April 4, 2025
KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayTM is a system for the precise monitoring, recordingPotential for microbial contamination.
- Class II
Medical Device Recall · April 3, 2025
Atalante X, Powered Exoskeleton. Atalante X is intended to perform ambulatory functions and mobility exercises, hands-free, in rehabilitation institutions under the supervision of a trained operatorPotential for exoskeleton to lose lateral balance and cause patient to fall.
- Class II
Food Recall · April 3, 2025
Sundae Shoppe, Cookies and Cream Mochi Ice Cream, 6 count, 7.5 oz, Plastic sealed tray inside paper carton. 6 Pieces per carton, 8 cartons per shipper. Keep frozen.Undeclared Wheat and Soy
- Class II
Medical Device Recall · April 3, 2025
MAGEC 2 Rod, 5.0mm 90mm Standard; Version/Model: MC2-5090S;Devices for the affected lot were not assembled according to product specifications. The distraction rod outer diameter was assembled with a 5.5mm rod versus the required 5.0mm.
- Class II
Food Recall · April 3, 2025
CHILE VERDE EGG BITES; NET WT. 4.6 OZ (130 g); 2 egg bites/packagePotential contamination with foreign materials.
- Class II
Medical Device Recall · April 3, 2025
Waldemar Link GmbH & Co. KG (Mfg Site)
L-Shaped Femoral Augment; Item Numbers: (1) 880-320/12 (Sz. 0 - cemented sm), (2) 880-320/22 (Sz. 0 - cemented lg), (3) 880-321/12 (Sz. 1-2 - cemented sm), (4) 880-321/22 (Sz. 1-2 - cemented lg), (5)The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
- Unclassified
Consumer Product Recall · April 3, 2025
HONEYJOY COMPANY, of Fontana, California
HONEYJOY Convertible and Foldable High ChairsThe recalled high chairs pose a suffocation risk because they were marketed for infant sleep and have an incline angle greater than 10 degrees, in violation of the CPSC's Infant Sleep Products Rule and the Safe Sleep for Babies Act.
- Class II
Medical Device Recall · April 3, 2025
Waldemar Link GmbH & Co. KG (Mfg Site)
Posterior Femoral Augment; Item Numbers: (1) 880-310/11 (Sz. 0 - cemented sm), (2) 880-310/21 (Sz. 0 - cemented lg), (3) 880-311/11 (Sz. 1-2 - cemented sm), (4) 880-311/21 (Sz. 1-2 - cemented lg), (5)The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
- Unclassified
Consumer Product Recall · April 3, 2025
AliExpress, of San Mateo, California
Foldable Travel Hair DryersThe handheld hair dryers lack an immersion protection device that can cause death or serious injury due to electrocution or shock hazards if it falls into water when plugged in. The hair dryers are in violation of the federal regulations and present a substantial product hazard.
- Unclassified
Vehicle Recall · April 3, 2025
Triumph Motorcycles America, Ltd.
2025 TRIUMPH SPEED TWIN 900Rear turn signals that are too close to the tail lights can cause difficulty seeing the motorcycle's intentions, increasing the risk of a crash.
- Class II
Drug Recall · April 3, 2025
Zydus Pharmaceuticals (USA) Inc
chlorproMAZINE Hydrochloride Tablets, USP 10 mg, Rx Only, 100 Tablets bottles, Manufactured by: Zydus Lifesciences Ltd., Baddi, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJCGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit
- Unclassified
Consumer Product Recall · April 3, 2025
American Honda Motor Co. Inc, of Torrance, California
Accessory Heaters for Model Years 2022-2024 Honda Pioneer 1000, 2023-2025 Pioneer 700, and 2022-2024 Honda Talon 1000 Side-by-Side vehiclesThe recalled accessory heaters can overheat and catch fire, posing fire and burn hazards to consumers.
- Class II
Food Recall · April 3, 2025
Label: IQF CILANTRO LARGE; NET WT: 30LB; PERISHABLE KEEP FROZEN; Packaging: blue plastic liner inside brown cardboard boxPotential contamination with foreign objects.
- Unclassified
Consumer Product Recall · April 3, 2025
Shen Zhen Cheng Cheng Ke Ji You Xian Gong Si, dba DualOranges Store, of China
Superb Sports Baby Bath SeatsThe recalled bath seats violate the federal safety regulation for infant bath seats, including requirements for stability and leg openings, and can tip over while in use, posing a risk of serious injury or death to babies due to drowning hazard.