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 the agency’s own highest classification or reported deaths or serious injuries, 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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151–175 of 114834

  • ModerateFDA (Devices)·Z-0242-2027·2026-10-28

    Boston Scientific Recalls Defective Direxion Torqueable Microcatheters

    Boston Scientific is recalling 76 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/SINGLE/027/BERN/1RO/105; Material Number: M001195430
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0199-2027·2026-10-28

    Philips Smart-hopping 2.0 AP Recall for Wireless Roaming Issues

    Philips North America is recalling 174 Smart-hopping 2.0 AP units due to unreliable wireless roaming behavior that can cause loss of connectivity to the central monitoring system.

    Product
    Philips Smart-hopping 2.0 AP 1.4 GHz; Product/Model Number: 867216;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0155-2027·2026-10-28

    El Ruisenor De Mexico Recalls Textured Soy Protein for Undeclared Soy

    El Ruisenor De Mexico, Inc. is recalling 123.5 pounds of Textured Soy Protein because the product contains soy, an allergen not declared on the label.

    Product
    Textured Soy Protein; packaged in 1lb, 5lb, 33lb clear plastic units. No UPC
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0237-2027·2026-10-28

    Boston Scientific Recalls Defective Direxion Torqueable Microcatheters

    Boston Scientific is recalling 748 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/SINGLE/021/BERN/2RO/130; Material Number: M001195340
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0104-2027·2026-10-28

    El Ruisenor De Mexico Recalls Black Sesame Seeds for Undeclared Allergen

    El Ruisenor De Mexico, Inc. is recalling black sesame seeds because the product contains an undeclared allergen ingredient (sesame).

    Product
    Black Sesame Seeds; packed in a clear plastic bag. 1lb, 5lb, 50lb unit size. No UPC
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0246-2027·2026-10-28

    Boston Scientific Recalls Defective Direxion Torqueable Microcatheters

    Boston Scientific is recalling 45 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/SINGLE/027/J/1RO/155; Material Number: M001195480
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0236-2027·2026-10-28

    Boston Scientific Recalls Defective Direxion Torqueable Microcatheters

    Boston Scientific is recalling 206 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/SINGLE/021/STRAIGHT/2RO/155; Material Number: M001195330
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0195-2027·2026-10-28

    Medtronic NDI Passive Spheres Recalled for Reflective Material Variation

    Medtronic is recalling NDI Passive Spheres because variation in the reflective material may affect the navigation system's ability to detect and track the spheres.

    Product
    Medtronic NDI Passive Spheres REF: 8801074, Sterile EO, 4/Tray 12 Pk., Rxonly
    Category
    Medical Device
    Distribution
    52 states
  • ModerateFDA (Food)·H-0153-2027·2026-10-28

    El Ruisenor De Mexico Recalls Raw Shelled Pistachios for Undeclared Allergen

    El Ruisenor De Mexico, Inc. is recalling raw shelled pistachios because the product contains an undeclared allergen. The recall involves 759 pounds of product distributed primarily in California.

    Product
    Raw Shelled Pistachios; packaged in 1lb, 5lb, 25-30lb clear plastic units. No UPC
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Drugs)·D-0059-2027·2026-10-28

    Pritam International Recalls evo Fluoride Toothpaste for CGMP Deviations

    Pritam International is voluntarily recalling 405,336 tubes of evo toothpaste nationwide due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    evo, Advanced Whitening, Anticavity Fluoride Toothpaste, (sodium fluoride 0.24%) Peppermint, Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-886-19, Item# 88619, UPC 8 10147 88619 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0055-2027·2026-10-28

    Pritam International Recalls Brush Buddies Toothpaste Due to CGMP Deviations

    Pritam International is voluntarily recalling 320,232 tubes of Brush Buddies toothpaste nationwide due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Brush Buddies, Crayola, Silly Scents, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Bubble Gum Flavor, Net Wt. 4.0 oz (113g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-003-40, Item # 32731, UPC 8 50048 32731 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0256-2027·2026-10-28

    Boston Scientific Recalls Direxion Torqueable Microcatheters Due to Defects

    Boston Scientific is recalling 378 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/FATHOM/027/STRAIGHT/1RO/155; Material Number: M001195720
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0064-2027·2026-10-28

    Brush Buddies Toothpaste Recalled for CGMP Deviations

    Pritam International is voluntarily recalling Brush Buddies toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Brush Buddies, Chocolate Ice Cream Flavored Toothpaste, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-518-35, Item # 88518, UPC 8 10147 88518 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0279-2027·2026-10-28

    Medline Tubal Ligation Kits Recalled for Adhesive Removal Issues

    Medline Industries is recalling three tubal ligation kits because they are difficult to remove from patients and leave adhesive residue on the skin.

    Product
    MEDLINE medical convenience kits labeled as: TUBAL LIGATION RFD, Medline Product Number/SKU DYNJ906291G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0197-2027·2026-10-28

    Medtronic Biopsy Needle Kit Recalled for Reflective Material Variation

    Medtronic is recalling 3,746 Biopsy Needle Kits because variation in the reflective material may affect the navigation system's ability to detect and track the spheres.

    Product
    Medtronic Biopsy Needle Kit, REF: 9733068, Passive, Sterile EO, Rxonly
    Category
    Medical Device
    Distribution
    52 states
  • ModerateFDA (Food)·H-0107-2027·2026-10-28

    El Ruisenor De Mexico Recalls Chocolate Covered Almonds for Undeclared Almond

    El Ruisenor De Mexico, Inc. is recalling 24.5 pounds of Chocolate Covered Almonds because the product contains an undeclared allergen ingredient, almond.

    Product
    Chocolate Covered Almonds; packed in a clear plastic bag. 1lb, 5lb, 50lb unit size. No UPC
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·H-0106-2027·2026-10-28

    El Ruisenor De Mexico Recalls Almonds in Shell for Undeclared Allergen

    El Ruisenor De Mexico, Inc. is recalling Almonds in Shell because the product contains an undeclared allergen ingredient (Almond).

    Product
    Almonds in Shell; packed in a clear plastic bag. 1lb, 5lb, 50lb unit size. No UPC
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0247-2027·2026-10-28

    Boston Scientific Recalls Direxion Torqueable Microcatheters for Coating Defects

    Boston Scientific is recalling 1,349 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/SINGLE/027/SWAN/1RO/130; Material Number: M001195500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0161-2027·2026-10-28

    El Ruisenor De Mexico Recalls Tube Shaped Wheat Snack for Undeclared Wheat

    El Ruisenor De Mexico, Inc. is recalling Tube Shaped Wheat Snack because it contains an undeclared wheat allergen. The product is sold in 1lb, 5lb, and 33lb clear plastic units.

    Product
    Tube Shaped Wheat Snack; packaged in 1lb, 5lb, 33lb clear plastic units. No UPC
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0230-2027·2026-10-28

    Boston Scientific Recalls Defective Direxion Torqueable Microcatheters

    Boston Scientific is recalling 1,912 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/SINGLE/021/J/1RO/130; Material Number: M001195270
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0062-2027·2026-10-28

    Pritam International Recalls Brush Buddies Toothpaste Due to CGMP Deviations

    Pritam International is voluntarily recalling 112,092 tubes of Brush Buddies Mint Chocolate Chip Ice Cream Flavored Toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Brush Buddies, Mint Chocolate Chip Ice Cream Flavored Toothpaste, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-520-35, Item # 88520, UPC 8 10147 88520 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0125-2027·2026-10-28

    Jovy Gummy Peach Rings Recalled for Undeclared Artificial Dyes

    El Ruisenor De Mexico, Inc. is recalling Jovy Gummy Peach Rings because the product contains undeclared artificial dyes Red #40, Yellow #5, and Yellow #6.

    Product
    Jovy Gummy Peach Rings; packed in a clear plastic 1lb unit sizes. UPC: 712199083404
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0258-2027·2026-10-28

    Boston Scientific Recalls Direxion Torqueable Microcatheters Due to Coating Defects

    Boston Scientific is recalling 432 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.

    Product
    Direxion Torqueable Microcatheter, NGMC/FATHOM/027/BERN/1RO/155; Material Number: M001195750
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0192-2027·2026-10-28

    Think Surgical Square Driver Recalled for Design Specification Failures

    Think Surgical is recalling 15 Square Driver units because they failed to meet design specifications, potentially causing pins to stick or wobble during drilling.

    Product
    Think Surgical Square Driver REF: 109126
    Category
    Medical Device
    Distribution
    Distributed nationwide