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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1651–1675 of 113805

  • HighFDA (Devices)·Z-2342-2026·2026-06-17

    MIC Safety 20 Fr push PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits, 20 Fr PUSH OTW, catalog number 7170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 901 kits affected.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2343-2026·2026-06-17

    MIC Safety 24 Fr push PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits, 24 Fr PUSH OTW, catalog number 7170-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 132 kits affected.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Product Description: Feeding Tube Kit Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2333-2026·2026-06-17

    CORFLO Safety PEG kit 30-4320 contains recalled lidocaine injection

    CORFLO Safety PEG Kits, catalog number 30-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 231 kits are affected.

    Product
    Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2401-2026·2026-06-17

    Bicarby dialysate bags carry an incorrect GTIN on the label

    Bicarby Dialysate, model RFP-400-G, is being recalled because of an error in the GTIN printed on the product, which could lead to a potassium concentration differing from the prescription.

    Product
    Bicarby Dialysate; Model number: RFP-400-G;
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2311-2026·2026-06-17

    Plum Solo Precision IV pumps may not display soft limit alerts

    Plum Solo Precision IV Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.

    Product
    Plum Solo Precision IV Pump, 40001-0401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2336-2026·2026-06-17

    CORFLO Safety PEG kit 30-6316 contains recalled lidocaine injection

    CORFLO Safety PEG Kits, catalog number 30-6316, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 41 kits are affected.

    Product
    Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2400-2026·2026-06-17

    Aluminum chloride hemostatic gel kits shipped with wrong package insert

    Advance Aluminum Chloride Gel Clear Hemostatic Gel Kits are being recalled because some units contain the package insert for Ferric Sulfate Gel, which gives different first aid instructions.

    Product
    Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2335-2026·2026-06-17

    CORFLO Safety PEG kit 30-6312 contains recalled lidocaine injection

    CORFLO Safety PEG Kits, catalog number 30-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 31 kits are affected.

    Product
    Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2327-2026·2026-06-17

    CGuard Prime 9mm by 30mm carotid stents may fail deployment

    CGuard Prime Carotid Stent Systems, 135 cm with a 9 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.

    Product
    CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2348-2026·2026-06-17

    MIC Safety 20 Fr push OTW PEG kits contain recalled lidocaine

    MIC Safety PEG Kits with ENFit Connectors, 20 Fr PUSH OTW, catalog number 8170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catalog Number: 8170-20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2346-2026·2026-06-17

    MIC Safety 24 Fr pull PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits, 24 Fr PULL, catalog number 7180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 1,006 kits affected.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2406-2026·2026-06-17

    MOSAIQ oncology software may fail to load adapted treatment plan

    The MOSAIQ Oncology Information System is being recalled because the software may fail to load an adapted baseline shift plan during treatment delivery when a communication error occurs.

    Product
    MOSAIQ Oncology Information System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2408-2026·2026-06-17

    Halyard towel six packs shipped without validated sterilization in Iowa

    Halyard Towel Six Packs, kit code AMTS70-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 224 kits affected.

    Product
    Halyard, Towel Six Pack. Kit Code: AMTS70-01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2314-2026·2026-06-17

    GE Allia IGS 3 Pulse systems pose shock risk to servicers

    Allia IGS 3 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. Nine units affected.

    Product
    Allia IGS 3 Pulse angiographic X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2356-2026·2026-06-17

    NexxZr dental zirconia discs may have reduced or missing dentin layer

    NexxZr T Multi A3.5 zirconia discs for all-ceramic dental restorations are being recalled because a reduced or missing dentin layer increases the risk of fracture in the mouth.

    Product
    NexxZr T Multi A3.5 W98-16mm, REF: 745451
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2280-2026·2026-06-17

    Fresh Roast ColorTrack instruments may allow excess infrared laser exposure

    Fresh Roast Systems ColorTrack instruments, model BENCH R-100, are being recalled because a manufacturing defect could allow access to infrared laser light above the product's safety classification.

    Product
    Fresh Roast Systems ColorTrack. Model Name: ColorTrack. Model Number: BENCH R-100
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·H-0913-2026·2026-06-17

    Estrella passion fruit drink does not declare FD&C Red 40

    Estrella Bebida de Parcha (Passion Fruit Drink) in three sizes is being recalled because of undeclared FD&C Red 40. A total of 2,111 units are affected.

    Product
    ESTRELLA, Bebida de Parcha (Passion Fruit Drink), multiple sizes, 14 OZ.FL. (413 ML), 64 OZ.FL (1,920mL), 120 OZ.FL. (3.54LT.) 14 OZ.FL Plastic Bottles packed in cases of 25 bottles. KEEP REFRIGIRATED.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0925-2026·2026-06-17

    Guava cake 47 ounce containers hold undeclared synthetic color additives

    Cake de Guayaba, 47 oz, is being recalled because of undeclared colors: Yellow #5, Yellow #6 and/or Red #40. 311 units are affected.

    Product
    Cake de Guayaba [image] Guava Cake The Original, Net Wt. 47 oz, packaged in a plastic container, one unit per container. KEEP REFRIGERATED. UPC 824790852782
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·H-0938-2026·2026-06-17

    Pasteurized donor human milk bottles show dark spot contamination

    MMB of Louisiana Pasteurized Donor Human Milk, 3 oz, is being recalled over potential physical contamination after a dark spot was noticed on the bottom of a container. 32 bottles affected.

    Product
    MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, Cal/Oz: 19, 0.9 g/dL Protein, packaged in a clear plastic bottle with white plastic cap
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0921-2026·2026-06-17

    Capuchino syrup cone cakes contain undeclared synthetic color additives

    Capuchino Syrup Cone Cake, 13 oz, is being recalled because of undeclared colors: Yellow #5, Yellow #6 and/or Red #40. 3,028 units are affected.

    Product
    Capuchino [image] Syrup Cone Cake The Original, Net Wt. 13 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852119
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·H-0929-2026·2026-06-17

    Marquesita mango flavored cakes contain undeclared synthetic color additives

    Marquesita de Mango flavored cakes, 16 oz, are being recalled because of undeclared colors: Yellow #5, Yellow #6 and/or Red #40. 442 units are affected.

    Product
    Marquesita de Mango [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852706
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·H-0919-2026·2026-06-17

    Guava rolls sold in Florida and Texas contain undeclared color additives

    Rollitos de Guava, 15 oz, are being recalled because of undeclared colors: Yellow #5, Yellow #6 and/or Red #40. 7,856 units are affected.

    Product
    Rollitos de Guava [image] Guava Rolls The Original, Net Wt. 15 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852454
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·H-0932-2026·2026-06-17

    Marquesita chocolate and vanilla cakes contain undeclared synthetic color additives

    Marquesita de Chocolate y Vainilla flavored cakes, 16 oz, are being recalled because of undeclared colors: Yellow #5, Yellow #6 and/or Red #40. 809 units are affected.

    Product
    Marquesita de Chocolate y Vainilla [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852706
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·H-0937-2026·2026-06-17

    Flan custard cake recalled for undeclared Yellow and Red dyes

    Flan Cake (Custard Cake), 30 oz, is being recalled because of undeclared colors: Yellow #5, Yellow #6 and/or Red #40. 423 units are affected.

    Product
    Flan Cake [image] Custard Cake The Original, Net Wt. 30 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852959
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2320-2026·2026-06-17

    EXCOR pediatric blood pump valves carry mismatched inner package expiration dates

    EXCOR Pediatric VAD System blood pump PU valves are being recalled because the inner package expiration date does not match the correct outer package date.

    Product
    EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF: P30P-001x01
    Category
    Medical Device
    Distribution
    Distributed nationwide