The Recall Desk

Archive

March 2024 recalls

556 recalls were announced in March 2024.

What the numbers show

Critical
24
Severe
151
High
334
Moderate
45
Low
2

Of the 556 recalls this month scored against our rubric, 4% are Critical, 27% are Severe.

501–556 of 556

  • HighFDA (Food)·F-0932-2024·2024-03-06

    Chin Jung White Kimchi Recalled Due to Undeclared Fish Allergen

    Chin Jung White Kimchi jars recalled due to undeclared fish allergen. Products distributed to supermarkets in California, Colorado, and Nevada may pose risk to consumers with fish allergies.

    Product
    Chin Jung White Kimchi - 7 lb. 8 oz.(3.4 kg) plastic jars
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0997-2024·2024-03-06

    Food: Gatorade Protein Bars Recalled Due to Potential Salmonella

    The Quaker Oats Co. is voluntarily recalling Gatorade Protein Bar Peanut Butter Chocolate with Best Before dates of Aug-02-24 and earlier due to potential Salmonella. The product was distributed nationally and internationally.

    Product
    Gatorade Protein Bar Peanut Butter Chocolate 2.8 oz; 1 count; 6 count; 12 count
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0956-2024·2024-03-06

    Quaker Chewy Dipps Peanut Butter recalled for potential Salmonella

    The Quaker Oats Co. is recalling Quaker Chewy Dipps Peanut Butter bars due to potential Salmonella contamination. The recall affects products with a Best Before date of Aug-02-24 or earlier.

    Product
    Quaker Chewy Dipps Peanut Butter 6ct 6.5 oz; 14ct 15.3 oz. Bars are individually wrapped in plastic and then packaged in paperboard boxes or totes.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0971-2024·2024-03-06

    Frito-Lay Snack Mix Variety Packs Recalled for Potential Salmonella

    The Quaker Oats Co. is recalling Frito-Lay Popped & Baked Chips variety packs for potential Salmonella contamination. Affected products have best-before dates of August 2, 2024 or earlier and were distributed nationally and internationally.

    Product
    Frito-Lay Popped & Baked Chips with Cookies, Nuts and Quaker Chewy Bars Variety Pack 40ct 35.58 oz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1001-2024·2024-03-06

    Reser's Amish Macaroni Salad recalled for undeclared wheat allergen

    Reser's Amish Macaroni Salad is recalled because some containers have a mislabeled side label that does not declare wheat, which is an ingredient in the product. This poses a risk to people with wheat allergies.

    Product
    The recalled Reser's Amish Macaroni Salad was packaged in a plastic clear container where the top lid is labeled as Reser's Amish Macaroni Salad, Net Wt. 1lb., and the container side label indicates Reser s Southern Style with Egg Potato Salad, Net Wt. 1lb. UPC 0 71117 19044 1.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0936-2024·2024-03-06

    Quaker Big Chewy Bars Chocolate Chip recalled for potential Salmonella

    The Quaker Oats Company is voluntarily recalling Quaker Big Chewy Bars Chocolate Chip due to potential Salmonella contamination. The product, distributed nationwide and internationally, affected millions of cases.

    Product
    Quaker Big Chewy Bars Chocolate Chip 5ct 7.4 oz, 1ct 1.48 oz, 10ct 14.8 oz. Bars are individually wrapped in plastic and packaged in paperboard boxes
    Category
    Food
    Distribution
    2 states
  • 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
  • HighFDA (Food)·F-0962-2024·2024-03-06

    Quaker Simply Granola Oats Cereal Recalled for Potential Salmonella

    Quaker Simply Granola Oats, Honey & Almonds Cereal with Best Before dates of Aug-02-24 or earlier is being recalled due to potential Salmonella contamination. The voluntary recall affects 22,512,942 cases distributed nationwide.

    Product
    Quaker Simply Granola Oats, Honey & Almonds Cereal; 2PK 48.2 oz; 24.1 oz.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0992-2024·2024-03-06

    Cereal Recall: Cap n Crunch OOPS! All Berries Due to Salmonella Risk

    The Quaker Oats Co. is recalling Cap n Crunch OOPS! All Berries Cereal (10.3 oz) due to potential Salmonella contamination. Products with a Best Before date of Aug-02-24 or earlier are affected nationally.

    Product
    Cap n Crunch OOPS! All Berries Cereal 10.3 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-0972-2024·2024-03-06

    Frito-Lay Snack Time Favorites Variety Pack Recalled for Potential Salmonella

    Frito-Lay has recalled Snack Time Favorites variety packs due to potential Salmonella contamination. Affected products have a Best Before date of August 2, 2024 or earlier and were distributed nationally and internationally.

    Product
    Frito-Lay Snack Time Favorites with Baked, Smartfood, SunChips and Quaker Chewy Granola Bars Variety Pack 40ct 33.94 oz
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0957-2024·2024-03-06

    Quaker Chewy Dipps snack bars recalled for potential Salmonella contamination

    The Quaker Oats Company is voluntarily recalling Quaker Chewy Dipps Variety Pack snack bars due to potential Salmonella contamination. The recall affects products distributed nationally across all U.S. states, territories, and some international markets.

    Product
    Quaker Chewy Dipps Variety Pack 14ct 15 oz; 48ct 51.6 oz Bars are individually wrapped in plastic and then packaged in paperboard boxes.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0951-2024·2024-03-06

    Quaker Chewy Bars Less Sugar recalled due to potential Salmonella

    Quaker Oats is recalling Quaker Chewy Bars Less Sugar variety across multiple package sizes due to potential Salmonella contamination. The recall affects products distributed nationally and internationally with Best Before dates of August 2, 2024 or earlier.

    Product
    Quaker Chewy Bars Less Sugar Variety 8ct 6.7 oz; 18ct 15.1 oz; 58ct 48.7 oz; 60ct 50.4 oz. Bars are individually wrapped in plastic and then packaged in paperboard boxes.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1002-2024·2024-03-06

    Zingerman's Bakehouse Brownie Recall Due to Undeclared Walnut Allergen

    Zingerman's Bakehouse is recalling Black Magic Brownie products due to undeclared walnut allergen. Affected consumers with walnut allergies should not consume the product.

    Product
    Zingerman's Bakehouse Black Magic Brownie, Individually Packaged, 4 oz., UPC 844397000706 Zingerman's Bakehouse Black Magic Brownie 4 Pack, 1 lb., UPC 844397008795
    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 (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-0350-2024·2024-03-06

    Mesalamine extended-release capsules recalled due to dissolution failure

    Sun Pharmaceutical is recalling Mesalamine extended-release capsules due to failed dissolution specifications. The affected capsules may not dissolve and release medication properly.

    Product
    MESALAMINE — MESALAMINE (MESALAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0351-2024·2024-03-06

    Equate Lubricant Eye Ointment Recalled for Lack of Sterility Assurance

    Equate Lubricant Eye Ointment, distributed nationwide by Walmart, is being recalled because the manufacturer cannot assure the product's sterility. The recall affects 315,842 units across multiple lots.

    Product
    Equate Lubricant Eye Ointment (Mineral Oil 42.5%, White Petrolatum 57.3%), Packaged in 3.5 gram tubes, Distributed by Walmart Inc., Bentonville, AR 72716, NDC 79903-026-35, UPC 681131395298
    Category
    Drug
    Distribution
    Distributed nationwide
  • 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 (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-0363-2024·2024-03-06

    Lidocaine and Phenylephrine Injectable Vials Recalled for Glass Delamination

    Denver Solutions is recalling Lidocaine-Phenylephrine injectable vials nationwide due to glass delamination in the vials. The defect could potentially introduce glass fragments into the medication.

    Product
    Lidocaine HCL 1% (10mg/mL), PHENYLephrine HCL 1.5% (15mg/mL), 1 ml in a Single- Dose Vial, RX Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-090-42
    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 (Devices)·Z-1210-2024·2024-03-06

    Olympus Colonoscope Recall: Missing Protective Adhesive in 47 Units

    Olympus is recalling 47 colonoscope units (Model PCF-H190DL) because they were assembled without protective adhesive. The missing adhesive may cause equipment failure under vibration, temperature changes, or shock.

    Product
    Colonoscope, Model Number PCF-H190DL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1182-2024·2024-03-06

    IdentiTi ALIF surgical graft bolts recalled due to intraoperative breakage

    Alphatec Spine recalls IdentiTi ALIF graft bolts after reports of breakage during implantation. Approximately 12,777 devices are affected worldwide.

    Product
    IdentiTi ALIF Standalone Interbody System: Part Number/Description 132-10-85-250 / IdentiTi ALIF SA Graft Bolt, 08.5 x 25 mm 132-10-85-300 / IdentiTi ALIF SA Graft Bolt, 08.5 x 30 mm 132-10-85-350 / IdentiTi ALIF SA Graft Bolt, 08.5 x 35 mm 132-10-90-250 / IdentiTi ALIF SA G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1198-2024·2024-03-06

    Integra Cranial Access Kit recalls due to packaging sterility defect

    Integra LifeSciences is recalling 161 units of the Cranial Access Kit (Lot 7124720) due to packaging defects that may compromise sterility. The recall affects units distributed worldwide.

    Product
    Ref No: INS7260 / 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-1207-2024·2024-03-06

    Colonoscope Model CF-HQ190L Recalled Due to Missing Protective Adhesive

    Olympus Corporation is recalling 97 Colonoscope Model CF-HQ190L units distributed nationwide. The devices were assembled without protective adhesive, risking malfunction under vibration, temperature changes, or shock.

    Product
    Colonoscope, Model Number CF-HQ190L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1199-2024·2024-03-06

    Integra Cranial Access Kit recall over sterile packaging defect

    Integra LifeSciences is recalling the Cranial Access Kit due to a defect in the sterile packaging that may compromise product sterility. Affects 30 units distributed worldwide.

    Product
    Ref No: INS7270 / 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-1197-2024·2024-03-06

    Integra Cranial Access Kit Recalled Due to Packaging Integrity Defect

    Integra LifeSciences is recalling 188 units of the Integra Cranial Access Kit because defective sterile packaging may have compromised product sterility.

    Product
    Ref No: INS7250 / 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-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-1200-2024·2024-03-06

    Integra Cranial Access Kit Recall Due to Sterile Packaging Defect

    Integra LifeSciences is recalling the INS7280 Cranial Access Kit due to a packaging defect that may compromise product sterility. The recall affects 82 units distributed worldwide.

    Product
    INS7280 / 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-1202-2024·2024-03-06

    Integra Cranial Access Kit Recalled for Defective Sterile Packaging

    Integra LifeSciences is recalling 915 units of its Cranial Access Kit worldwide due to defective sterile packaging that may compromise product sterility. The header bags failed required packaging integrity testing.

    Product
    Ref No: INSHITHND / 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 (Devices)·Z-1191-2024·2024-03-06

    Dialysis Accessory Device Recalled for Blood Leakage Risk

    The NxStage Cartridge Express dialysis device is recalled because blood can leak or spray from the arterial line. This could cause uncontrolled blood loss in patients or expose healthcare workers to infectious blood.

    Product
    NxStage Cartridge Express with Speedswap, Catalog No. CAR-535. An accessory device for facilitating the removal and replacement of a flow-compromised filter during treatment of acute and chronic renal failure or fluid overload.
    Category
    Medical Device
    Distribution
    19 states
  • 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-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 (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 (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-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-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 (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 (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·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·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·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·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
  • 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
  • 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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