The Recall Desk

Archive

July 2024 recalls

547 recalls were announced in July 2024.

What the numbers show

Critical
9
Severe
88
High
398
Moderate
49
Low
3

Of the 547 recalls this month scored against our rubric, 2% are Critical, 16% are Severe.

401–500 of 547

  • SevereNHTSA·24E059000·2024-07-09

    JecoEV Tesla to CCS Charging Adapter Recall for Fire and Shock Risk

    Dongguan Biaoming is recalling JecoEV Tesla to CCS charging adapters sold on Amazon due to missing over-temperature protection and insecure latching, posing fire and electrical shock risks.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:CHARGING:CABLE/CORD:ACCESSORY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V517000·2024-07-09

    2023 to 2024 Mercedes-Benz Sprinter Rear Suspension U-Bolt Recall

    Daimler Vans USA is recalling certain 2023-2024 Mercedes-Benz Sprinter vehicles due to rear suspension U-bolts with reduced strength from improper heat-treatment. The defect can cause the rear axle to shift, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V523000·2024-07-09

    Prevost buses recalled for defective wheelchair lift bridging device

    Prevost recalls certain 2005-2024 buses with wheelchair lifts due to a potentially steep bridging device that can cause wheelchair instability. Affected owners should contact Prevost for a free replacement.

    Product
    PREVOST — PREVOST X3-45, H3-45, H3-41, X3-45 COMMUTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V524000·2024-07-09

    Volvo Bus 9700 Recall for Steering Gear Link Rod Nut Tightening

    Volvo Bus is recalling 2024 9700 vehicles because improperly tightened nuts on the steering gear link rod may loosen, potentially causing loss of steering control.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V515000·2024-07-08

    Autocar Recalls 2023-2024 Xpeditor Trucks for Cab Tilt Hinge Pin Defect

    Autocar is recalling 841 2023-2024 Xpeditor trucks because a missing retaining ring on the cab tilt hinge pin could cause the pin to separate, creating a road hazard and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V518000·2024-07-08

    2021-2024 Nova Bus LFS Parking Brake Air Leak Recall

    Nova Bus is recalling 2021-2024 LFS buses due to an air leak in the parking brake valve that can cause unexpected parking brake engagement without activating brake lights, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V519000·2024-07-08

    Nova Bus LFS windshield wiper blade alignment defect recall

    Nova Bus is recalling certain 2022-2023 LFS buses due to incorrectly aligned windshield wiper arms that can cause wiper blades to collide. Damaged blades reduce visibility and increase crash risk.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V516000·2024-07-08

    2021-2022 Jeep Cherokee Curtain Airbag Connector May Fail to Deploy

    Chrysler is recalling 2021-2022 Jeep Cherokee vehicles with improperly secured right-side curtain airbag connectors that may prevent deployment, increasing injury risk in a crash.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·020-2024·2024-07-05

    Al-Safa Recalls Frozen Chicken Products Due to Listeria Contamination

    Al-Safa US LLC is recalling approximately 2,010 pounds of frozen ready-to-eat chicken products that may be contaminated with Listeria monocytogenes.

    Product
    Al-Safa US LLC Recalls Frozen Ready-To-Eat Chicken Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1424-2024·2024-07-03

    Pop a Nosh Mixed Munch snacks recalled for undeclared wheat

    AMB FOODS INC is recalling Pop a Nosh Mixed Munch snacks due to undeclared wheat allergen. Approximately 2,100 units distributed in New York contain wheat, which is not labeled on the product.

    Product
    Pop a Nosh Mixed Munch; Regular Flavor; 8oz plastic bag; Potato Chips, Popcorn, Pretzels; UPC 914669941
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-2140-2024·2024-07-03

    Life2000 Ventilator systems recalled due to battery charging failure risk

    The Life2000 Ventilator may fail to charge or experience intermittent charging behavior due to damage to the battery charger dongle. This FDA Class I recall affects approximately 2,510 units distributed nationwide.

    Product
    Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0002A and BT-20-0002AP. The Life2000 ventilation system includes the Life2000 ventilator which has its individual label.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1425-2024·2024-07-03

    Pop a Nosh Mixed Munch Snack Recalled for Undeclared Wheat Allergen

    Pop a Nosh Mixed Munch in Honey BBQ flavor is recalled due to undeclared wheat allergen. Approximately 2,100 units distributed in New York may lack proper allergen labeling.

    Product
    Pop a Nosh Mixed Munch; Honey BBQ Flavor; 8oz plastic bag; Potato Chips, Popcorn, Pretzels; UPC 914669941
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2163-2024·2024-07-03

    Philips SENSE XL TORSO COIL Recall Due to Potential Patient Burn Hazard

    Philips is recalling SENSE XL TORSO COIL units used in MRI imaging because the coils may heat up excessively and cause patient burns. This FDA Class I recall affects 729 units distributed worldwide.

    Product
    SENSE XL TORSO COIL 1.5T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567141882, 453567141883. Coils may be included in kits with Mode Numbers: 989603014351 & 989603014352.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1391-2024·2024-07-03

    ELV Control Herbal Supplement Recalled for Containing Toxic Yellow Oleander

    ELV Control Herbal Supplement is being recalled because it contains yellow oleander instead of the labeled tejocote ingredient. Yellow oleander is toxic to humans. The product was distributed through authorized dealers and e-commerce platforms.

    Product
    ELV Control Herbal Supplement; 90 Capsules
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1390-2024·2024-07-03

    Tejocote Root Products Recalled for Yellow Oleander Contamination

    GLOBAL MIX INC. is recalling Tejocote Root Products sold under multiple brand names because they contain Yellow Oleander, a toxic plant. Consumers should not use these products.

    Product
    Tejocote Root Products under the following brands: Eva Nutrition, Science of Alpha Mexican, NWL Nutra Mexican, and Niwali Mexican
    Category
    Food
    Distribution
    42 states
  • SevereFDA (Food)·F-1389-2024·2024-07-03

    Andersen & Sons Macadamia Nuts Recalled for Listeria Monocytogenes

    Andersen & Sons Shelling, Inc. is recalling its macadamia nuts due to Listeria monocytogenes contamination. Approximately 2,850 pounds were distributed in the United States.

    Product
    Andersen & Sons Shelling, Inc. Macadamia Nuts, Dry Roasted Style 6 25 lbs.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1422-2024·2024-07-03

    Green Life Farms Baby Arugula Recalled for Salmonella Contamination

    Green Life Farms Baby Arugula in 4.5 ounce clamshells has been recalled due to potential Salmonella contamination. The affected product has lot number LW15124 and a sell-by date of 6/15/24, distributed in Florida.

    Product
    Green Life Farms Baby Arugula in 4.5 ounce plastic clamshell packaging containers. 6 packages per case of 4.5oz each. Store in refrigerator.
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·24V509000·2024-07-03

    2025 Freightliner and Western Star Steering Tie Rod Assembly Defect

    Certain 2025 Freightliner and Western Star commercial vehicles may have improperly heat-treated tie rod assemblies that can fail, potentially causing loss of steering control and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 47X, CASCADIA, 49X, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2164-2024·2024-07-03

    Philips MR Torso Coil Recall: Potential Patient Burn Risk

    Philips is recalling 307 SENSE XL TORSO COIL 3.0T units used in MR imaging systems worldwide due to potential for coils to overheat and cause patient burn injuries.

    Product
    SENSE XL TORSO COIL 3.0T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567394941, 453567394942, 453567394943, 453567394945, 459801593182. Coils may be included in kits with Mode Numbers: 989603050641, 98960
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V513000·2024-07-03

    BMW Recalls 3 Series Vehicles Due to Air Bag Inflator Defect

    BMW is recalling 2006-2012 3 Series vehicles because a steering wheel air bag inflator may explode during deployment, posing a risk of serious injury.

    Product
    BMW — BMW 328I, 323I, 335XI, 335I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2159-2024·2024-07-03

    Inspire Model 3028 Implantable Pulse Generator Manufacturing Defect

    Inspire Medical Systems recalls the Model 3028 Implantable Pulse Generator due to a manufacturing defect causing electrical leakage and system malfunction that requires revision surgery. The recall affects 24 devices distributed in the US and Germany.

    Product
    Inspire Model 3028, IV Implantable Pulse Generator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1418-2024·2024-07-03

    Queso Chonero White Cheese Recalled for Listeria Contamination

    Queso Chonero Special White Cheese has been recalled due to Listeria monocytogenes contamination. The product was distributed in Illinois.

    Product
    Queso Chonero Special White Cheese UPC 7 861105 900496
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2165-2024·2024-07-03

    Philips SENSE XL Torso Coil 1.5T Recalled for Overheating Risk

    Philips recalled 14 SENSE XL Torso Coils worldwide due to potential overheating. The coils could heat up during use and cause patient burn injuries.

    Product
    SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567502281, 453567502282, 453567502283, 453567502284, 453567502285, 453567502286, 459801585212.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1403-2024·2024-07-03

    Wakefield Ham & Cheddar Pretzel Croissant Recalled for Possible Listeria Contamination

    Classic Delight LLC recalls Wakefield Ham & Cheddar Pretzel Croissant (1323 cases) due to possible Listeria monocytogenes contamination. Product distributed across 14 states with multiple lot numbers and best-by dates through March 2025.

    Product
    (Item 551697) Wakefield Ham & Cheddar Pretzel Croissant
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-2196-2024·2024-07-03

    Medtronic EVERA S VR Implantable Cardioverter Defibrillator Recalled for Manufacturing Defect

    Medtronic is recalling EVERA S VR implantable cardioverter defibrillators due to a potential manufacturing defect involving a weld crack that can cause device failure. The defect was identified during manufacturing leak testing.

    Product
    EVERA S VR, Model Number DVBC3D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1413-2024·2024-07-03

    Wakefield Bacon Cheeseburger Kaiser Rolls Possibly Contaminated with Listeria

    Classic Delight LLC is recalling Wakefield Bacon Cheeseburger Kaiser Rolls due to possible Listeria monocytogenes contamination. The recall affects 1,079 cases distributed across 14 states.

    Product
    (Item 806653) Wakefield Bacon Cheeseburger Kaiser Roll
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-2177-2024·2024-07-03

    Dental Scaler Tip May Not Seat Properly, Posing Injury Risk

    Dental EZ Group is recalling certain Titan Scaler Tip (Perio, Model 261669) units due to an oversized tip holder condition that may prevent proper seating, creating a risk of injury during use.

    Product
    Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler tip is used with an air drive scaler for subgingival scaling and fine access. The Perio tip is used for lingual supragingival scaling of mandibular incisors and deep local pockets.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2222-2024·2024-07-03

    Drainage Catheter Recalled Due to Incorrect Expiration Dates on Labels

    Cook Incorporated is recalling 15 units of the Ultrathane Mac-Loc Locking Loop Multipurpose Drainage Catheter due to incorrect expiration dates on product labels that extend beyond the device's true expiration date. Affected units were distributed to Spain and the Netherlands.

    Product
    Ultrathane Mac-Loc Locking Loop Multipurpose Drainage Catheter ULT16.0-38-25-P-6S-MCL-HC--Intended for percutaneous drainage in a variety of drainage applications (e.g., nephrostomy, biliary and abscess), either by direct stick or Seldinger access technique. ORDER NUMBER: GPN: G
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2200-2024·2024-07-03

    Medtronic PRIMO MRI DR SureScan Cardioverter Defibrillators Recalled for Manufacturing Defect

    Medtronic is recalling two PRIMO MRI DR SureScan implantable cardioverter defibrillators due to a potential manufacturing defect involving weld cracks detected during manufacturing quality testing.

    Product
    PRIMO MRI DR SureScan, Model Number DDMD3D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2188-2024·2024-07-03

    Siemens AXIOM Vertix Solitaire Display Fire Risk from Power Supply Short Circuit

    Siemens is recalling the AXIOM Vertix Solitaire diagnostic imaging component due to a short circuit in the Touch Display's power supply unit that may cause overheating and fire. Two units with serial numbers 1239 and 1241 are affected.

    Product
    ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is a component and has been specially designed for examining emergency and accident patients as well as for use in outpatient departments Material Number: 5901900
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1394-2024·2024-07-03

    Ready-to-Eat Turkey and Cheese Sandwiches Recalled for Possible Listeria Contamination

    Classic Delight LLC is recalling 384 cases of Classic Delight Turkey & Cheese On Round Bun (Item 6731) due to possible contamination with Listeria monocytogenes. The product was distributed to food service facilities in 14 states.

    Product
    (Item 6731) Classic Delight Turkey & Cheese On Round Bun - INSTITUTIONAL USE ONLY
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-2192-2024·2024-07-03

    Medtronic Implantable Defibrillator Recalled Due to Manufacturing Weld Crack

    Medtronic is recalling 14 Cobalt XT HF CDT-D MRI SureScan implantable defibrillators due to a manufacturing weld defect that could cause device failure.

    Product
    Cobalt XT HF CDT-D MRI SureScan, Model Number: DTPA2D4, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2197-2024·2024-07-03

    Medtronic Implantable Cardioverter Defibrillator Recalled for Manufacturing Weld Defect

    Medtronic is recalling 14 units of EVERA MRI S VR SureScan implantable cardioverter defibrillators (Model DVMC3D4) due to potential weld cracks discovered during manufacturing. No patient injuries have been reported.

    Product
    EVERA MRI S VR SureScan, Model Number DVMC3D4, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2205-2024·2024-07-03

    Medtronic MIRRO MRI ICD devices recalled for manufacturing weld crack defect

    Medtronic recalls 13 MIRRO MRI VR SureScan implantable cardioverter defibrillators (ICDs) due to a manufacturing weld crack. The defect was identified and caused device failure during the manufacturing leak check quality control test.

    Product
    MIRRO MRI VR SureScan, Model Number DVME3D4, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1412-2024·2024-07-03

    Blazin' Chicken Kaiser Rolls Recalled for Possible Listeria Contamination

    Classic Delight LLC is recalling 1,477 cases of Blazin' Chicken Kaiser Rolls due to possible Listeria monocytogenes contamination. The affected product has been distributed across multiple states.

    Product
    (Item 806661) Wakefield Blazin' Chicken Kaiser Roll
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-2203-2024·2024-07-03

    Implantable Cardioverter Defibrillator Recalled for Manufacturing Weld Defect

    Medtronic recalls 46 PRIMO MRI VR SureScan implantable cardioverter defibrillators due to a manufacturing defect. Weld cracks identified during manufacturing quality checks could cause device failure.

    Product
    PRIMO MRI VR SureScan, Model Number DVMD3D4, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2168-2024·2024-07-03

    GE CARESCAPE Canvas monitors may lose display following power loss events

    GE Healthcare medical monitors may fail to display following a power loss event after CPU battery replacement, potentially delaying patient condition recognition.

    Product
    CARESCAPE Canvas 1000, Model Numbers: a) 5865770; b) 5865770-01040169; c) 5865770-01054142; d) 5865770-01054696; e) 5865770-01054698; f) 5865770-01054721; g) 5865770-01054740; h) 5865770-01055202; i) 5865770-01055204; j) 5865770-01055270; k) 5865770-01055317; l) 5865
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1400-2024·2024-07-03

    Wakefield Bacon, Egg & Cheese Bagels recalled for possible Listeria contamination

    Classic Delight LLC is recalling 2,311 cases of Wakefield Bacon, Egg & Cheese Bagels (Item 514711) due to possible Listeria monocytogenes contamination. The affected product was distributed across 14 states.

    Product
    (Item 514711) Wakefield Bacon, Egg & Cheese Bagel
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-2176-2024·2024-07-03

    VASOVIEW HemoPro harvesting system fluid ingress may disable cautery

    Maquet Cardiovascular recalls VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems due to fluid ingress into the harvesting tool handle, which may prevent necessary cautery or cause unintended cautery during surgical procedures.

    Product
    The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2201-2024·2024-07-03

    Medtronic MIRRO MRI implantable defibrillator recalled for weld defect

    Medtronic is recalling 3 MIRRO MRI DR SureScan implantable cardioverter defibrillators due to a manufacturing weld crack that caused devices to fail quality checks. The defect was detected during manufacturing before devices reached patients.

    Product
    MIRRO MRI DR SureScan, Model Number DDME3D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2221-2024·2024-07-03

    Endoscopic Kittner Surgical Instrument Recalled for Sterile Barrier Defect

    ASPEN SURGICAL is recalling 1,900 units of the Endoscopic Kittner Blunt Dissecting Instrument (Model KT-9101) due to a potential defect in the sterile barrier seal.

    Product
    Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1417-2024·2024-07-03

    Marketside Cinnamon Pecan Braid Recalled for Undeclared Pecan Allergen

    The James Skinner Co. is recalling Marketside Cinnamon Pecan Braid Danish pastry due to incorrect labeling that fails to declare pecans. Consumers with pecan allergies who consume the product could experience allergic reactions.

    Product
    Marketside Cinnamon Pecan Braid, Triple-Filled Danish, Filled with Cinnamon Filling, Topped with Pecans, Sweet Icing and Streusel. Net Wt. 18 oz (1 lb 2 oz) 510g. UPC 7874202922. 6 units per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1416-2024·2024-07-03

    Turkey Sausage & Egg Muffins Recalled for Possible Listeria Contamination

    Classic Delight LLC is recalling 16,572 cases of Turkey Sausage & Egg Muffins (Item 73131) distributed across 14 states due to possible Listeria monocytogenes contamination.

    Product
    (Item 73131) Turkey Sausage & Egg Muffin
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-1410-2024·2024-07-03

    Wakefield Charbroiled Cheeseburgers Recalled Due to Listeria Contamination Risk

    Classic Delight LLC is recalling 1,626 cases of Wakefield Charbroiled Cheeseburgers due to potential Listeria monocytogenes contamination. The product was distributed to 14 states; consumers should discard affected items.

    Product
    (Item 806679) Wakefield Charbroiled Cheeseburger
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-1419-2024·2024-07-03

    Gluten-Contaminated Aussie Bites Bakery Product Recall Due to Allergen Mislabeling

    Universal Bakery Organic Aussie Bites are being recalled because they are labeled as gluten-free but testing found gluten content above 20 parts per million. The product was distributed to Washington and Illinois.

    Product
    Universal Bakery Organic Aussie Bites, 30 oz clamshell container
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1428-2024·2024-07-03

    Cream Cheese Stuffed Mini Bagels Recalled for Undeclared Gluten

    FEEL GOOD FOODS INC is recalling Cream Cheese Stuffed Everything Mini Bagels nationwide because the product contains gluten not listed on the label. Consumers with gluten sensitivity should not consume this product.

    Product
    Cream Cheese Stuffed Everything Mini Bagels
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1402-2024·2024-07-03

    Wakefield Charbroiled Cheeseburger Kaiser Roll Recalled for Listeria Contamination

    Classic Delight LLC is recalling 3,411 cases of Wakefield Charbroiled Cheeseburger Kaiser Roll due to possible Listeria monocytogenes contamination. The product was distributed in 14 states.

    Product
    (Item 514713) Wakefield Charbroiled Cheeseburger Kaiser Roll
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-1405-2024·2024-07-03

    Wakefield Ham, Egg & Cheese Muffins Recalled for Possible Listeria Contamination

    Classic Delight LLC is recalling 1,366 cases of Wakefield Ham, Egg & Cheese Muffins due to possible Listeria monocytogenes contamination. The affected products were distributed across 14 states.

    Product
    (Item 806604) Wakefield Ham, Egg & Cheese Muffin
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-1406-2024·2024-07-03

    Wakefield Ham, Egg & Cheese Croissant Recalled for Listeria Contamination

    Classic Delight LLC recalls Wakefield Ham, Egg & Cheese Croissants due to possible Listeria monocytogenes contamination. The product was distributed across 14 US states; consumers with affected products should not consume them.

    Product
    (Item 806612) Wakefield Ham, Egg & Cheese Croissant
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-1396-2024·2024-07-03

    Classic Delight Breaded Chicken Waffle Recalled for Possible Listeria Contamination

    Classic Delight Breaded Chicken Waffle (Item 7626) for institutional use is being recalled due to possible contamination with Listeria monocytogenes. The recall affects 644 cases distributed to institutions in 14 states.

    Product
    (Item 7626) Classic Delight Breaded Chicken Waffle - INSTITUTIONAL USE ONLY
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-1414-2024·2024-07-03

    Wakefield Sausage and Egg Pancake Recalled for Possible Listeria Contamination

    Classic Delight LLC recalls Wakefield Sausage & Egg Pancake products (Item 942821) due to possible Listeria monocytogenes contamination. Affected products were distributed across 14 states.

    Product
    (Item 942821) Wakefield Sausage & Egg Pancake
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-1423-2024·2024-07-03

    Fresh Catch Inc. Yellowfin Tuna Recalled for High Histamine Levels

    Fresh Catch Inc. is recalling Yellowfin Tuna for high histamine levels. No illnesses have been reported.

    Product
    Fresh Catch Inc. Yellowfin Tuna, 1 loin per case packaged in carboard boxes with keep refrigerated label
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2180-2024·2024-07-03

    X-ray Table Touch Display Power Supply Fire Hazard

    Siemens is recalling AXIOM MULTIX MT X-ray patient tables due to a potential short circuit in the Touch Display power supply that may cause overheating and fire. Fifty units were distributed nationwide.

    Product
    AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395399
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2198-2024·2024-07-03

    Medtronic EVERA MRI implantable defibrillator recalled for manufacturing weld defect

    Medtronic is recalling five units of its EVERA MRI S DR SureScan implantable cardioverter defibrillator due to a manufacturing defect—a weld crack that caused failure during quality control testing.

    Product
    EVERA MRI S DR SureScan, Model Number DDMC3D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V510000·2024-07-03

    Front airbag deployment defect in 2019 Alfa Romeo Stelvio

    Chrysler is recalling 2019 Alfa Romeo Stelvio vehicles for a defective seat belt buckle switch sensor that may prevent front airbags from deploying. Dealers will repair the connection at no cost.

    Product
    ALFA ROMEO — ALFA ROMEO, FIAT, JEEP STELVIO, GIULIA, 500E, 500X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24290·2024-07-03

    Tideway High-Speed Hair Dryers Recalled for Electrocution Hazard

    Focusee is recalling about 27,400 Tideway High-Speed Hair Dryers because they lack immersion protection and pose an electrocution or shock hazard if they fall into water while plugged in. Consumers should stop using the product immediately.

    Product
    Tideway High-Speed Hair Dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V512000·2024-07-03

    Alfa Romeo Stelvio and Giulia vehicles recalled for incorrect tire placard information

    Chrysler is recalling certain Alfa Romeo Stelvio and Giulia models with incorrect tire placard information. Incorrect tire pressure or size specifications can lead to under-inflation or wrong tires, increasing crash risk.

    Product
    ALFA ROMEO — ALFA ROMEO GIULIA, STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V511000·2024-07-03

    Freightliner Custom Chassis S2C and S2RV Brake Light Recall

    Daimler Trucks North America is recalling 2023-2025 Freightliner Custom Chassis S2C and S2RV trucks because brake lights may not illuminate during active brake assist events.

    Product
    FCCC — FCCC S2C, S2RV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2174-2024·2024-07-03

    Blood Glucose Meter Recall: Accu-Chek Guide May Display Incorrect Measurement Units

    Roche is recalling Accu-Chek Guide (SC) blood glucose meters that may display readings in mmol/L instead of mg/dL, appearing approximately 18 times lower than actual. This could lead to incorrect treatment decisions and long-term diabetes complications.

    Product
    Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm as an aid in monitoring the effectiveness of glucose control. Product REF Number: 08453071001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V506000·2024-07-03

    Motorhomes recalled for missing spare tire wheel bolts

    Tiffin is recalling certain motorhomes because the wheel bolts for the spare tire may be missing. A spare tire without correct bolts could detach and increase crash risk.

    Product
    TIFFIN — TIFFIN GH1, CONVOY, CAHABA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2167-2024·2024-07-03

    FDA Recalls CUSA Excel Surgical Handpiece for Housing Cracks

    Integra LifeSciences is recalling CUSA Excel C2600 surgical handpieces due to potential housing cracks that may delay treatment. The recall affects 2,652 units distributed nationwide and internationally.

    Product
    CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical procedures where fragmentation, emulsification and aspiration of soft and hard tissue Catalog Number: C2600* *Note: you may see C2600P or C2600SRL on labeling. This notice is applicable for those SKUs as w
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1430-2024·2024-07-03

    Chef Select Herb Baguettes Recalled for Undeclared Wheat and Milk Allergens

    Lidl US TRADING is recalling approximately 2,000 units of Chef Select 2 Herb Baguettes due to undeclared wheat and milk allergens resulting from foreign language labeling. Consumers with wheat or milk allergies should not consume this product.

    Product
    Chef Select 2 Herb Baguettes Filled With Herb Butter 2x175 g Barcode: 4056489447566. Frozen product packaged in a plastic bag, 2 baguettes per unit.
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1429-2024·2024-07-03

    Lidl Chef Select Garlic Baguettes Recalled for Undeclared Wheat and Milk Allergens

    Lidl US TRADING is recalling Chef Select 2 Garlic Baguettes due to undeclared wheat and milk allergens caused by foreign language labeling. Consumers with allergies to wheat or milk should not consume these products.

    Product
    Chef Select 2 Garlic Baguettes filled With Garlic Butter 2x175 g Barcode: 4056489447559. Frozen product packaged in a plastic bag, 2 baguettes per unit.
    Category
    Food
    Distribution
    10 states
  • HighCPSC·24288·2024-07-03

    American Honda Motor Recalls Off-Road Motorcycles for Grip Detachment

    American Honda Motor is recalling about 40,700 model year 2023-2024 off-road motorcycles (CRF50F, CRF110F, CRF125F) because the handlebar grip can detach, posing a crash and injury hazard. One crash resulting in a knee injury has been reported.

    Product
    Model Year 2023-2024 Off-Road Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24291·2024-07-03

    Hatch Baby Power Adapters for Rest 1st Generation Sound Machines Pose Shock Hazard

    Hatch Baby is recalling power adapters sold with Rest 1st Generation sound machines because the plastic housing can detach from the adapter when unplugged, exposing electrical prongs and creating a shock hazard. The firm has received 19 reports of the housing coming off, including two reports of minor electrical shock.

    Product
    Power Adapters sold with Rest 1st Generation sound machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1426-2024·2024-07-03

    Chocolate Chunk Cookie Mix Recalled for Undeclared Coconut Allergen

    Penguin Natural Foods is recalling 'THE PERFECT CHOCOLATE CHUNK COOKIE MIX Cravings by Chrissy Teigen' because the product contains undeclared coconut. Consumers with coconut allergies face a serious health risk.

    Product
    "THE PERFECT CHOCOLATE CHUNK COOKIE MIX Cravings by Chrissy Teigen NET WT. 15.76 OZ (447g)" Packaged in a beige cardboard box, with green lettering
    Category
    Food
    Distribution
    6 states
  • HighCPSC·24289·2024-07-03

    SWOMOG Children's Two-Piece Pajama Sets Recalled for Burn Hazard

    SWOMOG children's two-piece pajama sets sold on Amazon.com from May 2022 through January 2024 violate federal flammability standards for children's sleepwear, posing a burn hazard. Consumers should stop use immediately and contact SWOMOG for a full refund.

    Product
    SWOMOG Children's Two-Piece Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2219-2024·2024-07-03

    Stryker Hoffman LRF Wire Tensioner Adjustment Ring May Become Loose

    Stryker is recalling 39 Hoffman LRF Wire Tensioner devices because the adjustment ring may loosen, preventing proper tension setting. No injuries reported.

    Product
    Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2175-2024·2024-07-03

    Endoscopic Vessel Harvesting System Recalled Due to Potential Cautery Malfunction

    Maquet Cardiovascular recalls VasoView HemoPro 2 vessel harvesting systems due to potential fluid ingress that may prevent or unintentionally activate cautery function. The recall affects 430,037 units distributed worldwide.

    Product
    The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1. VasoView Hemopro 2, Model Number: VH-4000. 2. VasoView Hemopro 2 with Vasoshield. Model Number: VH-4001. The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting Systems are designed for use in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2211-2024·2024-07-03

    Medtronic ICD Implants Recalled for Manufacturing Weld Crack Defects

    Medtronic recalls 9 units of CROME VR MRI SureScan implantable cardioverter defibrillators due to a manufacturing weld crack that caused devices to fail quality control leak testing.

    Product
    CROME VR MRI SureScan, Model Number DVPC3D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1398-2024·2024-07-03

    Wakefield Southern Chicken Biscuit recalled for possible Listeria contamination

    Classic Delight LLC is recalling Wakefield Southern Chicken Biscuit (Item 176594) due to possible Listeria monocytogenes contamination. The product was distributed in 14 states with multiple affected lot numbers.

    Product
    (Item 176594) Wakefield Southern Chicken Biscuit
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-1407-2024·2024-07-03

    Wakefield Bacon, Egg & Cheese Bagels Recalled for Possible Listeria Contamination

    Classic Delight LLC is recalling Wakefield Bacon, Egg & Cheese Bagels (Item 806620) due to possible Listeria monocytogenes contamination. The recall affects 2,663 cases distributed across 14 states.

    Product
    (Item 806620) Wakefield Bacon, Egg & Cheese Bagel
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-2191-2024·2024-07-03

    Medtronic COBALT XT HF CRT-D implantable defibrillator recalled for manufacturing defects

    Medtronic is recalling 8 units of the COBALT XT HF CRT-D MRI SureScan implantable cardioverter defibrillator due to manufacturing defects identified during quality control testing.

    Product
    COBALT XT HF CRT-D MRI SureScan, Model Number: DTPA2D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2193-2024·2024-07-03

    Implantable Defibrillator Recalled for Manufacturing Weld Crack Defect

    Medtronic is recalling 11 units of the COBALT XT HF QUAD CRT-D MRI SureScan implantable cardioverter defibrillator due to a manufacturing defect involving weld cracks that failed quality control testing.

    Product
    COBALT XT HF QUAD CRT-D MRI SureScan, Model Number DTPA2Q1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2182-2024·2024-07-03

    Radiographic X-ray Table Recalled Due to Fire Hazard in Power Supply

    Siemens AXIOM MULTIX MP radiographic X-ray tables are being recalled due to a potential short circuit in the touch display's power supply unit that may cause overheating or fire. 12 units nationwide are affected.

    Product
    AXIOM MULTIX MP - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395381
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2210-2024·2024-07-03

    Medtronic Implantable Cardioverter Defibrillator Recalled for Manufacturing Defect

    Medtronic is recalling eight COBALT XT VR MRI SureScan implantable cardioverter defibrillators due to weld cracks that caused device failure during manufacturing.

    Product
    COBALT XT VR MRI SureScan, Model Number DVPA2D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1427-2024·2024-07-03

    Cream Cheese Stuffed Plain Mini Bagels Recalled for Undeclared Gluten

    FEEL GOOD FOODS INC is recalling Cream Cheese Stuffed Plain Mini Bagels due to undeclared gluten. Consumers with gluten sensitivity or celiac disease should not consume this product.

    Product
    Cream Cheese Stuffed Plain Mini Bagels
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2189-2024·2024-07-03

    Infinity M500 Cardiac Monitor Poses Electrical Shock Risk

    Draeger recalls 34,102 Infinity M500 monitoring systems due to electrical safety noncompliance. The devices pose a potential risk of electrical shock, burns, and cardiac arrhythmia.

    Product
    Infinity Acute Care System (IACS) Monitoring System, Infinity M500 with Power, Model No. MS20407. Rev 20, 21, and 23
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2181-2024·2024-07-03

    Siemens X-ray Table Recalled for Fire Hazard in Power Supply

    Siemens recalls AXIOM MULTIX MT radiographic X-ray tables due to a short circuit in the power supply unit that may cause overheating and fire. 7 units are affected nationwide.

    Product
    AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395415
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2213-2024·2024-07-03

    D*Clot® HD Rotational Thrombectomy System Recalled for Sterility Barrier Defect

    Mermaid Medical is recalling 190 D*Clot® HD Rotational Thrombectomy Systems worldwide due to failed sterility testing that indicates the sterility barrier may not be fully intact.

    Product
    The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous catheter-based system available in 6 French. The disposable system consists of an outer sheath through which a rotatable radiopaque spiral shaft extends ending in an eccentric blunt distal tip. Once activated, the s
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1408-2024·2024-07-03

    Frozen Sausage, Egg & Cheese Biscuits Recalled for Possible Listeria Contamination

    Wakefield Sausage, Egg & Cheese Biscuit (Item 806638) has been recalled in 14 states due to possible Listeria monocytogenes contamination. Affected products have best-by dates from February 2024 through March 2025.

    Product
    (Item 806638) Wakefield Sausage, Egg & Cheese Biscuit
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-2214-2024·2024-07-03

    RAPIDPoint 500e diagnostic system mislabels capillary blood samples as arterial

    Siemens RAPIDPoint 500e software version 5.3 incorrectly labels capillary blood samples as arterial on laboratory information system displays, potentially leading to misinterpretation of results and diagnostic errors.

    Product
    Software version 5.3 in: RAPIDPoint 500e Blood Gas System (USA) Siemens Material Number: 11416751 RAPIDPoint 500e Blood Gas System (China) 11416752; RAPIDPoint 500e Blood Gas System (Japan) 11416754; RAPIDPoint 500e Blood Gas System (ROW) 11416755 ;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2209-2024·2024-07-03

    Implantable defibrillator recalled for manufacturing defect causing device failure risk

    Medtronic is recalling five implantable defibrillators due to a manufacturing defect where weld cracks caused devices to fail quality testing. The defective devices were identified during manufacturing and did not reach patients.

    Product
    Cobalt XT DR MRI SureScan, Model Number DDPA2D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2215-2024·2024-07-03

    CentriMag Circulatory Support Console May Shut Down During Power Surge

    CentriMag Primary Console units may completely shut down without alarm during power surges above 1.8kV, requiring emergency switch to backup circulatory support.

    Product
    2nd Generation CentriMag Primary Console, REF: 201-90401, 201-90701, 201-90411, 201-90421, 201-30300, L201-90401, L201-90411, L201-90421, part of the CentriMag Circulatory Support System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2206-2024·2024-07-03

    Medtronic COBALT DR MRI ICD Recalled for Manufacturing Defect

    Nine Medtronic COBALT DR MRI implantable cardioverter defibrillators are recalled due to a weld crack that caused devices to fail manufacturing quality checks.

    Product
    COBALT DR MRI SureScan, Model Number DDPB3D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2179-2024·2024-07-03

    RingLoc Hip Acetabular Cup Recalled for Assembly Defect

    Biomet recalled RingLoc hip acetabular cup components that may have been incorrectly assembled with a mismatched locking ring, potentially causing joint instability. Affected patients may require surgical intervention.

    Product
    RingLoc Bi-Polar Hip System Acetabular Cup, 41 mm Outer Diameter - Used in hip hemi-arthroplasty Item Number: 11-165206
    Category
    Medical Device
    Distribution
    Distributed nationwide

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