The Recall Desk

Archive

March 2024 recalls

556 recalls were announced in March 2024.

What the numbers show

Critical
24
Severe
156
High
329
Moderate
45
Low
2

Of the 556 recalls this month scored against our rubric, 4% are Critical, 28% are Severe.

501–556 of 556

  • HighFDA (Devices)·Z-1203-2024·2024-03-06

    Integra Cranial Access Kit Recalled Due to Sterile Packaging Defect

    Integra LifeSciences is recalling the Cranial Access Kit due to a defect in sterile packaging that could compromise product sterility. The device is used for neurosurgical access to the brain.

    Product
    Ref No: INSHITHRZN / Integra Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0938-2024·2024-03-06

    Food Recall: Quaker Big Chewy Bars Potential Salmonella Contamination

    The Quaker Oats Co. has recalled Quaker Big Chewy Bars Variety Pack 36ct due to potential Salmonella contamination. The product was distributed nationally and in U.S. territories.

    Product
    Quaker Big Chewy Bars Variety Pack 36ct 53.3 oz Bars are individually wrapped in plastic and packaged in paperboard boxes.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0954-2024·2024-03-06

    Quaker Chewy Bars recalled due to potential Salmonella contamination

    The Quaker Oats Co. is voluntarily recalling Quaker Chewy Bars Variety Pack in multiple sizes due to potential Salmonella contamination. The product was distributed nationally and internationally.

    Product
    Quaker Chewy Bars Variety Pack 8ct 6.7 oz; 14ct 11.8 oz; 58ct 48.7 oz; 1ct 0.84 oz; 440ct 369.6 oz; 18ct 15.1 oz; 30ct 25.2 oz ;36ct 30.2 oz; 48ct 40.3 oz; 60ct 50.4 oz . Bars are individually wrapped in plastic and then packaged in paperboard boxes or totes.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0976-2024·2024-03-06

    Quaker Chewy Granola Bars recalled for potential Salmonella contamination

    The Quaker Oats Company has recalled Quaker Chewy Granola Bar (Fruity Fun, Splendid Strawberry) 0.84 oz packages due to potential Salmonella contamination. Approximately 22.5 million cases were distributed nationally and internationally.

    Product
    Quaker Chewy Granola Bar (Fruity Fun) Splendid Strawberry 0.84 oz 6 Count
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0933-2024·2024-03-06

    MUTTI Crushed Tomatoes Recall Due to Can Lining Detachment

    Mutti USA is recalling MUTTI Crushed Tomatoes because the internal can lining may be detaching into the product. The recall affects 137,634 units distributed to 24 states.

    Product
    MUTTI Crushed Tomatoes; Polpa; Net Wt 27.9 OZ (1lb 11.9 OZ) 790g; UPC 85469300071
    Category
    Food
    Distribution
    25 states
  • HighFDA (Food)·F-0965-2024·2024-03-06

    Quaker Chocolatey Favorites Snack Mix recalled for potential Salmonella

    The Quaker Oats Co. is recalling Quaker Chocolatey Favorites Snack Mix (Best Before Aug-02-24 and earlier) due to potential Salmonella contamination. The product was distributed nationally across all US states, Puerto Rico, Guam, Saipan, and internationally.

    Product
    Quaker Chocolatey Favorites Snack Mix; 20ct Box 378 oz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1213-2024·2024-03-06

    Colonoscope Model PCF-HQ190L Recalled for Missing Protective Adhesive

    Olympus is recalling 28 colonoscopes (Model PCF-HQ190L) due to missing adhesive that protects the device from vibration, temperature changes, and physical shock. The defect could cause device malfunction during procedures.

    Product
    Colonoscope, Model Number PCF-HQ190L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1217-2024·2024-03-06

    Orthopedic knee implant recall due to potential stem misalignment

    United Orthopedic Corporation recalls USTAR II knee implants due to potential incorrect orientation of the curved stem. Affected products were distributed across multiple US states and internationally.

    Product
    USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153109 - PE25151109 - 9x125mm, PE25151111 - 11X125, PE25151113 - 13X125mm, PE25151115 - 15X125mm, PE25151117 - 17X125mm, PE25151119 - 19X125mm, PE25151209 - 9X150mm, PE25151211…
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-1215-2024·2024-03-06

    Hip Implant System Recalled for Potential Incorrect Stem Orientation

    United Orthopedic Corporation is recalling the USTAR II Hip System Press-Fit Curved Stem due to a potential risk that the implant curved stem may be oriented incorrectly. The FDA Class II recall affects 598 units.

    Product
    USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers: REF: PE11151211 - 11x150mm, PE11151213 - 13x150mm, PE11151215 - 15x150mm, PE11151217 - 17x150mm, PE11151411 - 11x200mm, PE11151413 - 13x200mm, PE11151415 - 15x200mm…
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-0994-2024·2024-03-06

    Cap n Crunch Sea Berry Crunch Cereal Recalled Due to Potential Salmonella

    The Quaker Oats Co. is voluntarily recalling Cap n Crunch Sea Berry Crunch Cereal 15.5 oz boxes due to potential Salmonella contamination. The recalled products have a Best Before date of Aug-02-24 or earlier.

    Product
    Cap n Crunch Sea Berry Crunch Cereal 15.5 oz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0963-2024·2024-03-06

    Quaker Simply Granola Cereal Recalled for Potential Salmonella

    The Quaker Oats Co. is recalling Quaker Simply Granola Oats, Honey, Raisins & Almonds Cereal due to potential Salmonella. Affected products have Best Before dates of August 2, 2024, or earlier and were distributed nationally and internationally.

    Product
    Quaker Simply Granola Oats, Honey, Raisins & Almonds Cereal; 2PK 48.2 oz; 24.1 oz; 69 oz.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0953-2024·2024-03-06

    Quaker Chewy Bars S'mores recalled due to potential Salmonella

    The Quaker Oats Company is recalling Quaker Chewy Bars S'mores in multiple package sizes due to potential Salmonella contamination. The recall affects products distributed nationally and internationally.

    Product
    Quaker Chewy Bars S'mores 8ct 6.7 oz; 58ct 48.7 oz; 1ct 0.84 oz; 440ct 369.6 oz; 18ct 15.1 oz. Bars are individually wrapped in plastic and then packaged in paperboard boxes or totes.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1212-2024·2024-03-06

    Olympus colonoscope PCF-H190TL recalled for missing protective adhesive

    Olympus has recalled certain repaired colonoscope models lacking protective adhesive that could fail under vibration, temperature, or severe shock loads. Affected models include the PCF-H190TL, distributed nationwide.

    Product
    Colonoscope, Model Number PCF-H190TL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1208-2024·2024-03-06

    Colonoscope Model CF-Q180AL Recalled Due to Missing Protective Adhesive

    Olympus is recalling two colonoscopes (Model CF-Q180AL, serial numbers 2602060 and 2603763) due to missing protective adhesive that normally guards against vibration, temperature changes, and shock loads.

    Product
    Colonoscope, Model Number CF-Q180AL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0955-2024·2024-03-06

    Quaker Chewy Dipps Chocolate Chip bars recalled for potential Salmonella

    Quaker Chewy Dipps Chocolate Chip bars are being recalled nationwide due to potential Salmonella contamination. Affected products have a Best Before date of Aug-02-24 or earlier.

    Product
    Quaker Chewy Dipps Chocolate Chip 6ct 6.5 oz; 14ct 15.3 oz; 24ct 26.2 oz; 30ct 32.7 oz; 34ct 37.1 oz. Bars are individually wrapped in plastic and then packaged in paperboard boxes or totes.
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·24V177000·2024-03-06

    2022-2024 Triumph Speed Triple motorcycles recalled for engine overheating

    Triumph is recalling certain 2022-2024 Speed Triple RS and RR motorcycles because the engine may overheat and cause a coolant leak, increasing injury risk. Dealers will replace the engine software free of charge.

    Product
    TRIUMPH — TRIUMPH SPEED TRIPLE RS, SPEED TRIPLE RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1206-2024·2024-03-06

    Colonoscope Model CF-HQ190I recalled for missing protective adhesive

    Olympus is recalling certain repaired Model CF-HQ190I colonoscopes assembled without protective adhesive, which may cause equipment failure under vibration, temperature changes, or shock.

    Product
    Colonoscope, Model Number CF-HQ190I.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0939-2024·2024-03-06

    Food Recall: Quaker Chewy Bars Potentially Contaminated with Salmonella

    The Quaker Oats Company is recalling Quaker Chewy Bars and Dipps Variety Packs due to potential Salmonella contamination. The affected products were distributed nationally and internationally, and consumers should discard or return them.

    Product
    Quaker Chewy Bars and Dipps Variety Pack 14ct 13 oz and 58ct 58.6 oz. Bars are individually wrapped in plastic and packaged in paperboard boxes.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0359-2024·2024-03-06

    7 Eleven Hand Sanitizer Gel recalled for manufacturing facility deficiencies

    Seatex LLC is recalling 1,282 cases of 7 Eleven Hand Sanitizer Gel due to manufacturing facility deficiencies found during FDA inspection. The product was distributed nationwide.

    Product
    7 Eleven Hand Sanitizer Gel, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 1250 mL cases, Magnus 16005 Gateway Drive, Ste 300, Frisco, TX 75033
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0361-2024·2024-03-06

    Moxifloxacin Ophthalmic Injection Solution Recalled for Glass Particle Contamination

    Denver Solutions is recalling Moxifloxacin PF eye injection vials nationwide due to glass delamination in the vials. The affected product is used for eye surgery injections.

    Product
    Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt Solution (BSS) Sterile injection, Intracameral Use Only, Single- Dose Vial, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-096-42
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0966-2024·2024-03-06

    Quaker On The Go Snack Mix recalled due to potential Salmonella contamination

    The Quaker Oats Co. is recalling Quaker On The Go Snack Mix products due to potential Salmonella contamination. A total of 22,512,942 cases are affected, distributed in all states, Puerto Rico, Guam, and Saipan, as well as internationally, with a Best Before date of Aug-02-24 or earlier.

    Product
    Quaker On The Go Snack Mix; 20ct Box 344 oz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0353-2024·2024-03-06

    CVS Health Lubricant Eye Ointment recalled due to lack of sterility assurance

    CVS Health Lubricant Eye Ointment is being recalled nationwide due to lack of sterility assurance during manufacturing. The recall affects 159,334 units distributed in 3.5-gram tubes with lot numbers A2F03, A2I02, A2L02, A3C04, and A3H04.

    Product
    CVS Health Lubricant Eye Ointment (Mineral oil 31.9% Emollient, White petrolatum 57.7% Emollient), Packaged in in 3.5 gram tubes, Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, NDC 76168-707-35, UPC 050428634141
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1218-2024·2024-03-06

    Bone plates and surgical screws distributed without FDA pre-market clearance

    Acumed LLC is recalling 2,952,121 units of Acu-Loc bone plates, screws, and accessories distributed worldwide because they were placed on the market without FDA pre-market clearance. The safety and effectiveness of these devices have not been verified by the FDA.

    Product
    Acu-Loc and Acu-Loc 2 bone plates, screws and accessories for the following REF: 70-0045 Acu-Loc VDU Plate Standard, Left; 70-0045-S Acu-Loc VDU Plate Standard, Left; 70-0046 Acu-Loc VDU Plate Standard, Right; 70-0046-S Acu-Loc VDU Plate Standard, Right; 70-0047 Acu-Loc VDU…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1184-2024·2024-03-06

    Rebstock Holding Rod for Fixation May Move Uncontrollably

    The Rebstock Holding rod for fixation, a surgical instrument, may move or twist uncontrollably during use, potentially compromising patient safety if the movement transfers to attached equipment.

    Product
    Rebstock Holding rod for fixation -For holding and fixation of flexible Leyla Arms and spatula Art. No. 06-06-285 and 06-06-285MOD. surgical instrument.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1196-2024·2024-03-06

    Integra cranial access kit recalled for sterile packaging failure

    Integra LifeSciences is recalling 1,324 cranial access kits due to sterile packaging defects that may compromise product sterility.

    Product
    Ref No: INS5HND / Integra Cranial access kit (without Prep solutions) Bit and Guard. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0944-2024·2024-03-06

    Quaker Chewy Bars Chocolate Chip recalled for potential Salmonella

    The Quaker Oats Co. is recalling Quaker Chewy Bars Chocolate Chip Spring Minis nationwide due to potential Salmonella contamination. Affected products have a Best Before date of August 2, 2024, or earlier.

    Product
    Quaker Chewy Bars Chocolate Chip Spring Minis 28ct 13.8 oz. Bars are individually wrapped in plastic and packaged in paperboard boxes.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1194-2024·2024-03-06

    Integra Cranial Access Kit Recalled for Sterile Packaging Defect

    Integra LifeSciences is recalling 27 units of its Cranial Access Kit due to defective sterile packaging that may compromise product sterility. The kits were distributed worldwide.

    Product
    Ref No: HITHSP04 / Integra Cranial Access Kit. For access to the subarachnoid space or the lateral ventricles of the brain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1209-2024·2024-03-06

    Colonoscope Recall: Missing Protective Adhesive May Cause Device Failure

    Olympus Corporation is recalling 18 colonoscopes with missing adhesive that protects against physical stress. The missing protective adhesive could allow device failure under vibration, temperature fluctuation, or shock.

    Product
    Colonoscope, Model Number PCF-H180AL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0934-2024·2024-03-06

    Frozen Pizza Recalled for Undeclared Milk Allergen in Plant-Based Product

    Oggi Plant-Based Americana frozen pizza contains undeclared milk, posing a risk to consumers with milk allergies. The recall affects 5,040 units distributed in California, Illinois, and Washington.

    Product
    Oggi Pizza Plant Based Americana Beyond Meat Crumbles on Cauliflower Crust, gluten-free frozen pizza - cook before serving, net wt. 13.76oz (390g). One pizza wrapped in plastic film in a cardboard box. Retail box UPC 6 28451 68487 9. There are 12 pizza per case, and each case…
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0935-2024·2024-03-06

    Quaker Chewy Bars Peanut Butter Chocolate Chip recalled for potential Salmonella

    The Quaker Oats Co. is recalling Quaker Chewy Bars Peanut Butter Chocolate Chip due to potential Salmonella contamination. Affected products were distributed nationally and internationally with best-before dates of August 2, 2024 or earlier.

    Product
    Quaker Chewy Bars Peanut Butter Chocolate Chip: 8ct 6.7 oz; 18ct- 15.1 oz; 58ct 48.7 oz; 1ct -0.84oz; 440ct 369.6 oz. Bars are individually wrapped in plastic and packaged in paperboard boxes
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0352-2024·2024-03-06

    Equate Stye Lubricant Eye Ointment recalled due to sterility assurance failure

    Equate Stye Lubricant Eye Ointment is being recalled due to lack of assurance of sterility. Approximately 355,633 units have been distributed nationwide and are affected.

    Product
    Equate Stye Lubricant Eye Ointment (Mineral Oil 31.9%, White Petrolatum 57.7%), Packaged in 3.5 g tubes, Distributed by Walmart Inc., Bentonville, AR 72716, NDC 79903-028-35, UPC 681131395304
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1214-2024·2024-03-06

    Colonoscope Model PCF-Q180AL Recalled Due to Missing Protective Adhesive

    Olympus Corporation of the Americas is recalling Colonoscope Model PCF-Q180AL units that were assembled without protective adhesive. This missing adhesive protects the device from vibration, temperature fluctuations, and physical shock during use.

    Product
    Colonoscope, Model Number PCF-Q180AL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1192-2024·2024-03-06

    Dental Prosthetic Material Recall for Machining Defects

    GRAPHENANO Dental G-CAM denture manufacturing material is being recalled due to machining errors that render the product unusable. The recall affects 354 units distributed in Utah.

    Product
    GRAPHENANO DENTAL G-CAM, Product Codes: a) 95 Multichroma 14LB2, REF GC00089; b) 95 Multichroma 24LA2, REF GC00112; c) 95 Multichroma 20LA1, REF GC00130; d) 95 Multichroma 24LC2, REF GC00090; e) 95 Multichroma 24LA1, REF GC00113; f) 95 Multichroma 16LB2, REF GC00131…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1185-2024·2024-03-06

    EMD Millipore Issues Recall of Schiff Reagent Hotchkiss-McManus for Discoloration

    EMD Millipore has recalled Schiff Reagent Hotchkiss-McManus (lots 3094 and 3096) because units appear pink instead of colorless. Laboratories should discontinue use of affected units distributed to US states and Canada.

    Product
    Schiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a black polypropylene cap.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1190-2024·2024-03-06

    Abbott M1000 Wash Station Shipped Without U.S. Approval or Registration

    Abbott Molecular recalled M1000 Wash Station units shipped to U.S. customers without FDA approval or registration. The devices were intended for export only and not approved for U.S. distribution.

    Product
    Wash station: M1000 Wash Station Assembly & DITI Slide, REF 04J72-28* (*This part number is a spare to the M2000sp.)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0357-2024·2024-03-06

    Hand Sanitizer Recalled Nationwide for Manufacturing Practice Deficiencies

    Seatex LLC is recalling PROBLEND E3 Foaming Hand Sanitizer due to manufacturing practice deviations identified during FDA inspection. The recall affects products distributed nationwide in the US and Puerto Rico.

    Product
    PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0358-2024·2024-03-06

    7 Eleven Hand Sanitizer Recalled for Manufacturing Deficiencies

    A hand sanitizer distributed to 7-Eleven gas stations nationwide is being recalled due to manufacturing deficiencies identified during an FDA inspection. The affected product is lot 251176, distributed in the United States and Puerto Rico.

    Product
    7 Eleven FOR GAS ISLAND USE ONLY, Hand Sanitizer, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 330 Gal. cases, Distributed by: Magnus, 16005 Gateway Drive, Suite 300, Frisco, TX 75033
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1188-2024·2024-03-06

    Abbott in-vitro diagnostic kits shipped without U.S. approval or registration

    Abbott Molecular shipped two in-vitro diagnostic FISH probe kits to U.S. customers that were intended for export only and not approved or registered per U.S. specifications. The recall affects 16 kits distributed across eight states.

    Product
    In-vitro diagnostic kits: (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit, REF 01N15-010; (2) Abbott Vysis LSI D13S319 (13q14.3) SpectrumOrange Probe, REF 01N34-020;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0356-2024·2024-03-06

    FDA Recalls PROBLEND Hand Sanitizer for Manufacturing Deviations

    Seatex LLC is recalling 1,450 cases of PROBLEND Antibacterial Foaming Hand Sanitizer due to Current Good Manufacturing Practice (CGMP) deviations discovered at its manufacturing facility. The recall affects product distributed nationwide in the United States and Puerto Rico.

    Product
    PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser, Benzalkonium Chloride 0.13% Antibacterial, a) 1250 mL cases, b) 1 G cases, mountain spring scent, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0930-2024·2024-03-06

    Healthprint Vitamin D3 5000 recalled for sub-potency and incorrect labeling

    Ancient Formulas' Healthprint Vitamin D3 5000 supplement contains less Vitamin D than claimed and has incorrect daily value labeling. The recall affects 111 bottles distributed in Florida.

    Product
    Healthprint Vitamin D3 5000 Dietary Supplement, 200 tablets, packaged in plastic bottle.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1189-2024·2024-03-06

    Abbott Vysis Diagnostic Kits Recalled for U.S. Regulatory Non-Compliance

    Abbott Molecular recalls five Vysis in-vitro diagnostic kits that were intended for export and shipped to U.S. customers without approval or registration per U.S. specifications.

    Product
    In-vitro diagnostic kits: (1) Abbott Vysis LSI ATM (11q22.3) SpectrmOrange Probe, REF 01N33-020; (2) Abbott Vysis PTEN/CEP 10 FISH Probe Kit, REF 04N62-020; (3) Abbott Vysis TelVysion 1p SpectrumGreen Probe, REF 05J03-001; (4) Abbott Vysis TelVysion 4P SpectrumGreen Probe…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0360-2024·2024-03-06

    PROBLEND Hand Sanitizer Recalled Due to Manufacturing Deficiencies

    Seatex LLC is recalling PROBLEND Hand Sanitizer (Lot 266029) nationwide due to manufacturing deficiencies identified during FDA inspection.

    Product
    PROBLEND Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic, mountain spring scent, 1250 mL cases, Seatex LLC, 445 TX Hwy 36 Rosenberg, YX 77471
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1204-2024·2024-03-06

    FDA Recalls Conductive Adhesive Gel for Viscosity Defect

    Parker Laboratories is recalling Tensive Conductive Adhesive Gel due to five complaints regarding incorrect viscosity. The affected product was distributed across multiple US states and internationally.

    Product
    Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains 12 inner boxes with 50g tubes packaged in each.
    Category
    Medical Device
    Distribution
    10 states
  • SevereNHTSA·24E021000·2024-03-05

    Lippert Utility Hub Oil Seals Recalled for Brake System Leak Risk

    Lippert is recalling Utility Hub Oil Seals that may leak oil onto brake components, potentially reducing braking ability and increasing crash risk.

    Product
    POWER TRAIN:AXLE HUBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V175000·2024-03-05

    Incorrect Tire Placard Weight Labels on 2023-2024 Alfa Romeo Tonale and Dodge Hornet

    The tire placard label on certain 2023-2024 Alfa Romeo Tonale and Dodge Hornet vehicles displays an incorrect maximum vehicle capacity weight value, which could lead to vehicle overloading and increased crash risk. Dealers will add an overlay label to correct the information.

    Product
    DODGE — DODGE, ALFA ROMEO HORNET, TONALE PHEV, TONALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V176000·2024-03-05

    2024 Nissan Pathfinder and Infiniti QX60 Seat Belt Pretensioner Recall

    Nissan North America is recalling certain 2024 Nissan Pathfinder and Infiniti QX60 vehicles. The left-side front lap seat belt pretensioner may be improperly secured due to a missing rivet, which could prevent proper occupant restraint during a crash.

    Product
    NISSAN — NISSAN, INFINITI PATHFINDER, QX60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V174000·2024-03-04

    2023 NOVA BUS LFS recall—missing electrical components for battery switch

    Certain 2022-2023 NOVA BUS LFS vehicles may have missing electrical components that prevent the battery disconnect switch from functioning properly, creating a risk of electrical shock during maintenance.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·010-2024·2024-03-02

    Trader Joe’s Chicken Soup Dumplings Recalled for Foreign Matter

    CJ Foods Manufacturing Beaumont Corporation is recalling Trader Joe’s Steamed Chicken Soup Dumplings due to possible contamination with hard plastic from a permanent marker pen.

    Product
    CJ Foods Manufacturing Beaumont Corporation — CJ Foods Manufacturing Beaumont Corporation Recalls Trader Joe’s Chicken Soup Dumplings Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V170000·2024-03-01

    Mercedes-Benz Recalls G-Class Vehicles for Incorrect Air Conditioning Refrigerant

    Mercedes-Benz is recalling 2022-2023 G 550 and AMG G 63 vehicles because the air-conditioning system may contain incorrect refrigerant, which could leak and increase fire risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G 550, AMG G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V166000·2024-03-01

    Mercedes-Benz Recalls 2023 Sprinter Vans Due to Wiring Harness Fire Risk

    Daimler Vans USA is recalling 2023 Mercedes-Benz Sprinter vans because the main wiring harness may chafe and short circuit, increasing the risk of fire and loss of vehicle control.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 4500, SPRINTER 2500, SPRINTER 3500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V169000·2024-03-01

    2018-2023 Kia Stinger Turbocharger Oil Leak Engine Fire Risk

    Kia is recalling 2018-2023 Stinger and 2019-2020 K900 vehicles due to potential engine fire from deteriorating turbocharger oil feed pipes.

    Product
    KIA — KIA STINGER, K900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V171000·2024-03-01

    Winnebago Recalls 2024 Solis Motorhomes Due to Electrical Outlet Defect

    Winnebago is recalling 2024 Solis motorhomes because the lavatory may have a standard outlet instead of a GFCI protected one, increasing the risk of electric shock.

    Product
    WINNEBAGO — WINNEBAGO SOLIS
    Category
    Vehicle
    Distribution
    Distributed nationwide

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