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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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

2701–2725 of 30649

  • HighFDA (Devices)·Z-1052-2026·2026-01-21

    Medline IV Administration Kits Recalled Due to Check Valve Malfunction

    Medline is recalling IV administration kits containing B. Braun administration sets because check valve components may become stuck in open or closed positions. Ninety-six units were distributed nationwide.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-LE FORT MANDIBLE PACK-LF, Medline Kit SKU DYNJ0785864R; 2) RR-ASC EAR PACK-LF, Medline Kit SKU DYNJ0792607R.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0274-2026·2026-01-21

    Children's Nyquil Cold & Flu Recalled for Sanitation Defect

    Gold Star Distribution is recalling Children's Nyquil Cold & Flu due to insanitary conditions, including rodent exposure, at the distribution center. Consumers should not use affected products.

    Product
    CHILDREN NYQUIL, COLD&FLU, BERRY, 8oz, 12ct
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0390-2026·2026-01-21

    FDA Recalls Shrimp Paste for High Lead Contamination

    Shrimp paste manufactured by GUSTO GROUP, INC. has been recalled due to high lead levels detected in testing. The affected product was distributed to Iowa and New Jersey.

    Product
    DPA161 Shrimp Paste (Klong Kone) 'L' , 32 oz, 12 count , PLastic Jar, 12 packages / cases
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0384-2026·2026-01-21

    Banana Pudding Ice Cream recalled for undeclared soy lecithin allergen

    House Of Flavors, Inc. is recalling certain 3-gallon containers of 1972 Banana Pudding Ice Cream due to undeclared soy lecithin, a major allergen not listed on the label.

    Product
    1972 Banana Pudding Ice Cream, 3 GAL, UPC 0 75196 00556 6
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·H-0397-2026·2026-01-21

    Ukrop's Pound Cakes Recalled for Undeclared Soy Allergen

    Ukrop's Homestyle Foods is recalling Ukrop's 6-inch and 8-inch Pound Cakes because the products contain soy that is not declared on the label, posing a risk to consumers with soy allergies.

    Product
    Ukrop's 6" Pound Cake with Buttercream Icing/Red Roses NET WT 30 OZ (2.06lb/936g) UPC 7 22515 91452 7 and Ukrop's 8" Pound Cake with Buttercream Icing/Red Roses NET WT 44 OZ (2.75lb/1.25kg) UPC 7 22515 91456 5 CONTAINS: Egg, Milk, Wheat Made in a production area that also uses so
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0396-2026·2026-01-21

    Ukrop's 6-Inch Pound Cake Recalled for Undeclared Soy

    Ukrop's Homestyle Foods is recalling its 6-inch Pound Cake with Buttercream Icing due to undeclared soy. Consumers with soy allergies should not consume this product.

    Product
    Ukrop's 6" Pound Cake with Buttercream Icing/Pink Roses NET WT 44 OZ (2.75lb/1.25kg) CONTAINS: Egg, Milk, Wheat Made in a production area that also uses soy and tree nuts. UPC 7 22515 91452 7 Ukrop's Homestyle Foods, LLC Richmond, VA 23230
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0388-2026·2026-01-21

    Cinnamon Spice Product Recalled Due to Elevated Lead Contamination

    EUREKA INC cinnamon product recalled due to elevated lead levels. Product distributed to retail and wholesale customers in California and Michigan.

    Product
    Cinnamon, Clear Plastic Container, 100G, UPC 6251136 034139
    Category
    Food
    Distribution
    0 states
  • HighFDA (Drugs)·D-0262-2026·2026-01-21

    Aleve medication recalled nationwide due to insanitary distribution center conditions

    Aleve 1's, 60 CT tablets are recalled nationwide because Gold Star Distribution's facility had insanitary conditions including rodent activity. Consumers should stop using the affected product and consult their healthcare provider.

    Product
    Aleve 1's, 60 CT
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0284-2026·2026-01-21

    LUCKY ICE Cool Mouthwash Recalled for Potential Rodent Contamination

    LUCKY ICE Cool Mouthwash is being recalled due to insanitary conditions at the distributor's facility, including rodent exposure and activity. The product was distributed nationwide.

    Product
    LUCKY ICE, Cool Mouthwash, Alcohol Free, 16.9oz, 12CT, UPC: 808829108989
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0386-2026·2026-01-21

    Tops Strawberry Jam recalled for unapproved food color additive

    Mangalm LLC is recalling Tops Strawberry Jam because it contains carmoisine, an unapproved food color in the United States. The affected batch was distributed in California.

    Product
    Tops Strawberry Jam INGREDIENTS: Sugar, Strawberry Pulp 30%, Gelling Agent (Pectin - INS 440), Acidity Regulator (Citric Acid - INS 330), Preservative (Sodium Benzoate - INS 211, Potassium Metabisulphite - INS 224), Food Colour (Carmoisine - INS 122), Nature Identical Flavouring
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0280-2026·2026-01-21

    Swan alcohol recalled for insanitary conditions and rodent exposure

    Swan White Clear Alcohol (50%, 16oz bottles) distributed nationwide is being recalled due to insanitary conditions including rodent exposure and activity in the distribution center.

    Product
    Swan, White Clear Alcohol, 50%, 16oz, 12 count
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0276-2026·2026-01-21

    Pepcid Complete recalled due to rodent exposure in distribution facility

    Gold Star Distribution is recalling Pepcid Complete 25CT tablets nationwide due to CGMP deviations, including insanitary conditions and rodent activity discovered in their distribution center.

    Product
    PEPCID COMPLETE - 25CT
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1063-2026·2026-01-21

    Philips Allura Xper FD10F Medical Imaging System Electrical Short-Circuit Risk

    Philips is recalling 12 Allura Xper FD10F angiography systems worldwide because the cooling system's drip tray may not be installed. Without the tray, coolant could contact electrical components and cause short-circuits leading to system shutdown.

    Product
    Allura Xper FD10F; Model Number: 722002;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1064-2026·2026-01-21

    Allura Xper FD10 medical imaging system recalled for cooling drip tray issue

    Philips recalls 93 Allura Xper FD10 imaging systems due to missing or undocumented drip tray installations, which could allow coolant to contact electrical components and cause system shutdown.

    Product
    Allura Xper FD10; Model Number: 722003;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1040-2026·2026-01-21

    CT X-ray System Component Recalled for Missing Safety Label

    Mobius Imaging is recalling 101 AIRO CT X-ray system pendant components lacking the required 'Safe Hand Position Warning' label, which informs operators of proper positioning during use.

    Product
    Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1043-2026·2026-01-21

    Vanta Clinician Programmer Application versions recalled for software malfunction

    Medtronic recalls versions 2.0.2465 and 2.0.2683 of the Vanta Clinician Programmer Application. The software does not function as intended, creating potential for prolonged or postponed surgical procedures.

    Product
    A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1079-2026·2026-01-21

    Philips Azurion X-ray Systems software defect may cause imaging loss and system failures

    Philips Azurion X-ray imaging systems may experience nine software issues causing loss of X-ray imaging, system restarts, and diagnostic tool misalignment. 990 units distributed worldwide are affected.

    Product
    Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Number: 722229. 2. Azurion 3 M15. Model Number: 722230. 3. Azurion 5 M12. Model Number: 722231. 4. Azurion 5 M20. Model Number: 722232. 5.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1055-2026·2026-01-21

    Medline IV Administration Kits Recalled for Check Valve Malfunction

    Medline has recalled multiple kits containing B. Braun IV administration sets because the check valve components may become stuck in open or closed positions. The recall affects 3,045 units distributed nationwide.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DRAWER 2 IV SUPPLIES, Medline kit SKU ACC010271B; 2) DRAWER 2 IV FLUIDS & TUBING, Medline kit SKU ACC010416B; 3) OXYGENATION & TUBING TRAY, Medline kit SKU ACC010525C; 4)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1024-2026·2026-01-21

    Measurement Spectrometer Laser Safety Defect from Cable Failure

    The MAVERICK Measurement Module Spectrometer has a cable defect that can cause elevated laser output (approximately 1,600 mW) or unintended laser firing during measurement cycles. No injuries have been reported.

    Product
    MAVERICK¿ Measurement Module Spectrometer PN 820-01367 (originally part of a kit PN 820-01519) Finished Goods PN 820-01496
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1051-2026·2026-01-21

    Medline IV Administration Kits recalled for stuck check valve defect

    Medline is recalling certain pre-op kits due to check valve defects in IV and pump administration sets. The valves may become stuck in either position, potentially impairing medication delivery.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DELUXE PRE OP KIT, Medline SKU DYKS2034A; 2) DELUXE PRE OP KIT, Medline SKU DYKS2006B.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1100-2026·2026-01-21

    Arterial blood sampling kits recalled for cracked syringe collars and leakage risk

    ICU Medical is recalling certain Pulsator Arterial Blood Sampling Kits due to cracks in the syringe collar that may cause blood leakage or delayed delivery during arterial sampling.

    Product
    Pulsator Arterial Blood Sampling Kit, Item Numbers 4044EG-1 4080P-2 4084P-1 4080PE 4080PG
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1076-2026·2026-01-21

    Philips imaging system missing cooling unit drip tray installation

    Certain Philips Allura Xper FD20/10 imaging systems may lack a required drip tray beneath the cooling unit. If missing, coolant could contact electrical components and cause system shutdown.

    Product
    Allura Xper FD20/10; Model Number: 722029;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1018-2026·2026-01-21

    MRI systems recalled for potential helium vessel rupture during emergency discharge

    Canon Medical's VANTAGE TITAN 3T MRI systems may develop ice in the magnet vent system, which could trap helium gas and cause vessel rupture if an emergency discharge occurs, releasing pressurized helium into the scanning room.

    Product
    VANTAGE TITAN 3T Model MRT-3010/MEXL-3010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1091-2026·2026-01-21

    Philips Azurion medical imaging systems recalled for software defects

    Philips is recalling Azurion diagnostic imaging systems with software versions R2.1.10 and R2.2.10 due to six software defects that may cause system restarts, storage issues, and positioning errors. Approximately 10,466 units distributed worldwide are affected.

    Product
    Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Numbers: 722063, 722221. 2. Azurion 3 M15. Model Numbers: 722064, 722222, 722280. 3. Azurion 5 M12. Model Num
    Category
    Medical Device
    Distribution
    Distributed nationwide