Safety Recalls

15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 5,751–5,800 of 15,271

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  Mini Multi TEE Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Food Recall · July 3, 2025

  Evergreen Orchard Farm, LLC

  Evergreen Farm Jujube Juice, 4 fl. oz. (120ml) , Foil pouches, 25 foil pouches per case, Refrigerate product after opening

  Lack of pasteurization and sanitation records

  Class II

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  S9-2 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  C6-2 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  C8-4v Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  L9-3 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  X7-2 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  C8-5 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  L12-4 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Orascoptic Surgical Acuity

  Orascoptic Superior Visualization Phantom Nose Pad Accessory Kit ( nose pad and screw) 1 pk. and 20 pk.

  Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.

  Class II

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  C9-2 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  X5-1 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  C8-4v Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  3D9-3v Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  L18-5 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  VL13-5 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  S4-1 Lumify Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  D2cwc Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  mL26-8 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  eL18-4 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  mC12-3 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  L12-4 Lumify Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  C9-4v Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  3D6-2 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  S8-3t Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  D5cwc Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  Transducer C10-3v Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  X11-4t Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  L12-3 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Medical Device Recall · July 3, 2025

  Philips Ultrasound, Inc

  c5-1 Transducer Probe

  To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

  Class III

• Consumer Product Recall · July 3, 2025

  Harbor Freight Tools, of Calabasas, California

  Predator 2000W Power Stations

  The wires in the power station's AC outlet receptacles are reversed when the product is in Emergency Power Supply ("EPS") mode, posing a shock hazard to consumers operating the power station.

  Unclassified

• Consumer Product Recall · July 3, 2025

  Positec Tool Corporation, of Charlotte, North Carolina

  Hyper Tough, Worx and Portland Chainsaws and Pole Saws

  The main switch on the recalled chainsaws and pole saws can fail, allowing the saws to continue to run even after the switch is released, posing a laceration hazard.

  Unclassified

• Consumer Product Recall · July 3, 2025

  Yiwu Dixikeji Douxiangongsi, of China

  SNLN Party Supply Toys

  The recalled party supply toys violate the mandatory standard for toys containing button cell batteries because the compartment that holds the batteries can be easily accessed and opened by children, posing a deadly ingestion hazard to 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 · July 3, 2025

  Trane U.S. Inc., of Davidson, North Carolina

  Trane and American Standard Gas/Electric Packaged Units

  The fuel gas valve can open unexpectedly, allowing a gas leak and posing a fire hazard.

  Unclassified

• Food Recall · July 2, 2025

  WINDY CITY ORGANICS LLC

  SunBiotics Activated Almonds Infused with Probiotics, Oat Milk Chocolate, NET WT. 1 oz(28g) packaged in cases.

  Salmonella Contamination. Firm detected salmonella on one batch of our SunBiotics Oat Milk Chocolate Covered Almonds.

  Class I

• Vehicle Recall · July 2, 2025

  Jayco, Inc.

  2023 ENTEGRA LAUNCH

  A fuel leak in the presence of an ignition source increases the risk of a fire.

  Unclassified

• Vehicle Recall · July 2, 2025

  Nikola Corporation

  2024 NIKOLA TRE FCEV

  A damaged tank can leak fuel, increasing the risk of a fire.

  Unclassified

• Vehicle Recall · July 2, 2025

  Grand Design RV, LLC

  2023 GRAND DESIGN SOLITUDE, 2024 GRAND DESIGN SOLITUDE

  A broken step increases the risk of injury.

  Unclassified

• Food Recall · July 2, 2025

  LEWIS BAKERIES

  Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/2 Loaf of white bread with white flour topping and two splits on top 7/13/2025 - Best By Flexible plastic bag

  Undeclared allergen: Hazelnut due to mispackaging. Product with hazelnuts was put in the Artisan Style 1/2 loaf bags. Bags do not have allergen statement that includes hazelnuts.

  Class II

• Vehicle Recall · July 2, 2025

  Forest River, Inc.

  2025 FOREST RIVER ROCKPORT

  The fasteners can fail, causing the system to detach from the wall and increasing the risk of injury.

  Unclassified

• Medical Device Recall · July 2, 2025

  Stryker Corporation

  Stryker SmartPump Tourniquet, disposable sterile (single use) DISP 18X3,1BLA,1PRT QUICK / 5921-018-135; DISP 18X3,1BLA,2PRT QUICK / 5921-018-235; DISP 24X4,1BLA, 2PRT QUICK / 5921-024-235

  Tourniquet cuff flange may become detached from the bladder. If leak occurs during the procedure, there may be risk of hemorrhage, resulting in blood loss greater than expected. Other serious risks include cerebral hypotension and cardiovascular collapse and arrest, risking stroke or death. Specific to IVRA, patient toxicity may also occur due to rapid systemic absorption of anesthetics.

  Class II

• Medical Device Recall · July 2, 2025

  GE Medical Systems, LLC

  GE HealthCare OEC 9900 Elite C-arm Systems.

  GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.

  Class II

• Vehicle Recall · July 2, 2025

  KTM North America, Inc.

  2024 HUSQVARNA FE 350S

  A broken front brake caliper can cause a loss of front brake function, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · July 2, 2025

  GE Medical Systems, LLC

  GE HealthCare OEC 9800.

  GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.

  Class II

• Vehicle Recall · July 2, 2025

  Volvo Car USA, LLC

  2025 VOLVO EX90

  A loss of headlight function while driving can reduce visibility and increase the risk of a crash.

  Unclassified

• Medical Device Recall · July 2, 2025

  Spark Biomedical Inc

  Sparrow Ascent Patient Controller, REF's: 11-110-K, 11-310-K, 11-320-K, 11-321-K, 11-310-K-28, 11-320-K-28, 11-321-K-28

  Due to manufacturing issue, neurostimulator device may experience "cable disconnect" error message and interruption to stimulation output.

  Class II

• Drug Recall · July 2, 2025

  Lupin Pharmaceuticals Inc.

  Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg, 100 Capsules bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL, 34108, United States, Manufactured by: Lupin Limited,

  Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 instead of Jan.2027

  Class II

• Food Recall · July 2, 2025

  Alpine Slicing and Cheese Conversion Company

  Boar's Head Smoked Gouda, Net Wt 8 oz (226g). UPC 0 42421-50006 6. Keep Refrigerated. Distributed by Brunckhorst Co., NY,NY 11206.

  Mislabeling

  Class III

• Medical Device Recall · July 1, 2025

  Carefree Surgical Specialties

  Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk 25pk/CS Model/Catalog Number: 15505/25 Product Description: Rob

  Due to two issues: 1. Product contamination (biological foreign matter) that could compromise sterility. 2. Incorrect quantity of gauze in sterile packaging

  Class II

• Medical Device Recall · July 1, 2025

  Carefree Surgical Specialties

  Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Roll Gauze + Tail Medium 4 Long X-Ray Detectable 5pk 25pk/CS Roll Gauzes Model/Catalog Number: 15506/25 Product

  Due to two issues: 1. Product contamination (biological foreign matter) that could compromise sterility. 2. Incorrect quantity of gauze in sterile packaging

  Class II