The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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15926–15950 of 31567

  • HighFDA (Food)·F-0664-2024·2024-01-10

    Dietary supplement recalled due to potential mold contamination

    Spring Valley Biotin & Collagen Liquid is being recalled due to potential mold contamination. Approximately 24,324 units were distributed nationwide; consumers should stop using affected products.

    Product
    Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor, 15000 mcg, Dietary Supplement 29 doses 1 fl oz (29mL) UPC: 194346065158 Packaged in a glass bottle in a paper carton
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0663-2024·2024-01-10

    Bobo's Oat Bars Recalled for Undeclared Coconut Allergen

    Bobo's Oat Bars - Peach are recalled due to undeclared coconut. The recall affects approximately 10,800 units sold under Lot Code 3J27111.

    Product
    Bobo's Oat Bars - Peach 3oz packaged in ALOX coated PET film, corrugate cartons and master case. 12 units per carton
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0633-2024·2024-01-10

    Xstar Kojo slit knife recalled for incorrect blade orientation

    One lot of Xstar Kojo Safety Slit Knife contains inverted blades (bevel down instead of bevel up). The 2160 affected units from lot 6049877 were distributed internationally, including to Japan.

    Product
    Xstar Kojo Safety Slit Knife, 2.5mm 45¿ Bevel Up, Part Number 373025
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0635-2024·2024-01-10

    EDS 3 CSF External Drainage System recalled for incomplete sterility testing

    Natus Medical is recalling 3,336 units of the EDS 3 CSF External Drainage System nationwide because incomplete bioburden testing cannot guarantee sterility. No illnesses have been reported, but non-sterile devices pose infection risk.

    Product
    EDS 3 CSF External Drainage System, REF: NT821731C, STERILEEO, Rx only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0632-2024·2024-01-10

    Surgical Knife Crescent Recall Due to Incorrect Blade Angle

    Beaver Visitec International is recalling one lot of surgical knives where the blade is oriented incorrectly—bevel down instead of the required 55-degree bevel up. This defect could compromise surgical precision during use.

    Product
    Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·24V734000·2024-01-10

    2025 International HX and LT vehicles recalled for fuel pump fracture risk

    Navistar is recalling 2025 International HX and LT vehicles with Cummins X15 diesel engines due to fuel pump barrel fracture risk. The fracture can cause fuel leaks and engine stalls, increasing crash risk.

    Product
    INTERNATIONAL — 2025 INTERNATIONAL HX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V731000·2024-01-10

    2020-2023 Porsche Taycan Recalled for High-Voltage Battery Short Circuit Risk

    Porsche is recalling 2020-2023 Taycan vehicles due to a potential short circuit in the high-voltage battery that increases fire risk. Owners should limit charging to 80% until dealers replace the affected battery modules.

    Product
    PORSCHE — 2021 PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0634-2024·2024-01-10

    External Drainage System Collection Bags Recalled for Sterility Assurance Issues

    Natus Medical Incorporated is recalling 2,686 units of External Drainage System Collection Bags due to incomplete bioburden testing that prevents sterility assurance. Healthcare facilities and patients should contact the manufacturer or their healthcare provider for guidance.

    Product
    External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0692-2024·2024-01-10

    Frozen marinated milkfish recalled due to botulism risk from missing storage instructions

    Foremost Foods International is recalling Pamana Premium Marinated Bangus due to potential botulism risk. The frozen product in reduced oxygen packaging lacks required freezing and thawing instructions.

    Product
    Pamana Premium Marinated Bangus (Deboned Marinated Milkfish), Net Weight to be Weight at Time of Sale
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0623-2024·2024-01-10

    Medtronic Protege GPS Stent System Recalled for Packaging Seal Defects

    Medtronic is recalling Protege GPS Self-Expanding Peripheral Stent Systems due to seal defects in product packaging that could compromise sterility. Affected lot B644679 had national distribution.

    Product
    Protege GPS Self-Expanding Peripheral Stent System, product number SERB65-09-60-80, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0639-2024·2024-01-10

    Spinal fixation screws recalled due to incorrect size laser marking

    Zimmer Biomet Spine Inc. is recalling Vitality Polyaxial Screws (7.5mm x 50mm) due to incorrect laser marking showing 7.5 x 40. Incorrect screw size could cause perforation and vascular damage during spinal surgery.

    Product
    Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixation System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0629-2024·2024-01-10

    Microcatheter and Infusion Systems Recalled Due to Sterility Concerns

    Merit Medical Systems is recalling specific lots of microcatheter and infusion system devices because their sterility cannot be guaranteed. The devices were distributed worldwide including multiple US states and international locations.

    Product
    Fountain, REF: IS4-135-30 and IS4-90-10, CE2797, STERILEEO, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0689-2024·2024-01-10

    Seafood Medley Recalled for Potential Plastic Foreign Object

    Wegmans Seafood Medley (1 lb packages, Lot 47117) is being recalled because it may contain plastic foreign objects. The recall affects products distributed in Massachusetts, Pennsylvania, and New York.

    Product
    Wegmans Seafood Medley, 1lb.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0693-2024·2024-01-10

    Frozen Milkfish Recall Due to Missing Storage and Thawing Instructions

    Foremost Foods International is recalling Pamana Premium Bangus Belly frozen milkfish because the reduced-oxygen packaging lacks instructions to keep the product frozen and to thaw it properly, risking Clostridium botulinum toxin formation.

    Product
    Pamana Premium Bangus Belly (Cut Deboned Milkfish Belly), 340 g (120 oz)
    Category
    Food
    Distribution
    6 states
  • HighNHTSA·24V733000·2024-01-10

    Winnebago motorhomes recalled for defective turn signals

    Winnebago Industries recalls multiple motorhome models because turn signals may have insufficient lens area, making them difficult for other drivers to see and increasing crash risk. Dealers will replace the turn signals at no cost.

    Product
    WINNEBAGO — 2022 WINNEBAGO FORZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0691-2024·2024-01-10

    Marinated Baby Milkfish Recalled for Botulism Risk Due to Missing Storage Instructions

    Foremost Foods is recalling Pamana Premium Marinated Baby Bangus due to potential botulism risk. The frozen product in reduced-oxygen packaging lacks required freezing and thawing instructions.

    Product
    Pamana Premium Marinated Baby Bangus (Deboned Marinated Baby Milkfish), Net Weight to be Weight at Time of Sale
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0638-2024·2024-01-10

    Philips Trilogy Evo respiratory devices recalled for missing contraindication statement

    Philips recalled Trilogy Evo respiratory devices for missing contraindications in labeling. Devices lack warnings against use in pediatric patients under 10 kg and certain therapy modes, risking barotrauma and respiratory complications.

    Product
    Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B DS2110X11B EE2100X15B EE2110X15B ES2100X15B ES2110X15B EU2100X15B EU2100X19 EU2110X15B FR2100X14B FR2110X14B FX2100X15B GB2110X15B IA2100X15B IA21
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0627-2024·2024-01-10

    Merit Maestro Microcatheter Sterility Recall, 717 Units Distributed Worldwide

    Merit Medical Systems is recalling 717 units of Merit Maestro Microcatheters because their sterility cannot be guaranteed. Non-sterile devices could introduce infection when used in medical procedures.

    Product
    Merit Maestro Microcatheter, Reference Numbers: 28MC2111045/B, 28MC21110ST/B, 28MC2113045/B, 28MC21130SN/CNB, 28MC21130ST/B, 28MC2115045/B, 28MC2115045/C, 28MC21150SN/B, 28MC21150ST/B, 28MC2411045/D, 28MC24110SN/D, 28MC24110ST/D, 28MC2413045/D, 28MC24130SN/F, 28MC2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0631-2024·2024-01-10

    Covidien Valleylab FT10 Energy Platform software issue causes inoperability

    Covidien is recalling Valleylab FT10 FT Series Energy Platform devices due to a software issue that may render new systems inoperable. The recall affects 47,901 units distributed worldwide.

    Product
    Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0628-2024·2024-01-10

    FDA Recalls Merit Pursue Microcatheter Due to Sterility Concerns

    Merit Medical Systems is recalling Merit Pursue Microcatheter devices distributed worldwide because sterility cannot be guaranteed. Patients should contact their healthcare provider.

    Product
    Merit Pursue Microcatheter, REF: 28HC17130SN, 28HC17150ST/A, 29HC2015045/A, 29HC20150SN/A, 29HC20150ST, CE 2797, STERILEEO, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0218-2024·2024-01-10

    Peritoneal Dialysis Solution Recalled for Lack of Sterility Assurance

    Fresenius Medical Care is recalling 69,590 bags of DELFLEX Peritoneal Dialysis Solution due to lack of sterility assurance. The affected lot was distributed nationwide.

    Product
    DELFLEX — DELFLEX (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0215-2024·2024-01-10

    OTC Cough Medicine Recalled for Potential Water Contamination Risk

    Seaway Pharma Inc. recalled Premier Value Tussin Cough DM due to possible microbial contamination in manufacturing water. No contamination was found in finished products and no illnesses have been reported.

    Product
    Premier Value Tussin Cough DM, Dextromethorphan HBr...Cough Suppressant, Guaifenesin...Expectorant, Alcohol Free, 8 FL OZ (237 mL) bottle, Distributed by: Pharmacy Value Alliance, LLC, 407 East Lancaster Avenue, Wayne PA 19087, UPC 8-40986-03789-4.
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0624-2024·2024-01-10

    Serology ToRCH positive control specimen recalled for decreased HSV reactivity

    Randox Laboratories recalls SEROLOGY ToRCH lgM 2022 POSITIVE CONTROL (Lot 157SR) due to decreased HSV Type 1/2 reactivity when tested on the DiaSorin Liaison XL analyzer. The product was distributed in New York and West Virginia.

    Product
    SEROLOGY ToRCH lgM 2022 POSITIVE CONTROLI Intended for use with in vitro assays for determination of IgM antibodies to Cytomegalovirus (CMV), IgM antibodies to Rubella Virus, IgM antibodies to Toxoplasma gondii, IgM antibodies to Herpes Simplex Virus Type 1 and 2. Catalog Number
    Category
    Medical Device
    Distribution
    2 states