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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1–25 of 594

  • CriticalFDA (Devices)·Z-2604-2026·2026-07-08

    Omnipod DASH Pod insulin pump affected by external cannula damage

    Insulet Corporation is recalling Omnipod DASH Pods worldwide due to external soft cannula damage during manufacturing that can cause insulin to leak around the pod instead of being delivered. This may lead to high blood glucose levels and, in severe cases, diabetic ketoacidosis or death.

    Product
    Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 (5-Pack), POD-BLE-I1-520 (Single Pod). 2. POD-BLE-I1-529 (10-Pack), POD-BLE-I1-520 (Single Pod). 3. BLE-I1-529 (10-Pack), BLE-I1-520 (Single Pod). 4. BLE-C1-529 (10-Pack), BLE-C1-520 (Single
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·26600·2026-07-02

    Junpower CR2032 Lithium Coin Batteries Recalled for Ingestion Hazard

    Junpower CR2032 Batteries (20-piece packs) lack required child-resistant packaging and warning labels. If swallowed, these lithium coin batteries can cause serious internal injuries or death.

    Product
    Junpower CR2032 Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26515·2026-05-28

    Anzmtosn Luminous Fidget Spinner Balls Recalled for Battery Ingestion Risk

    Anzmtosn Luminous Fidget Spinner Balls are recalled because the included mini flashlight contains easily accessible button cell batteries that can cause serious internal injuries or death if swallowed by children.

    Product
    Anzmtosn Luminous Fidget Spinner Balls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26508·2026-05-28

    MiniWarGaming and Primal Horizon Disc Magnets Violate Mandatory Safety Standard

    MiniWarGaming Inc. and Primal Horizon are recalling approximately 22,624 disc magnets that violate mandatory safety standards. The high-powered magnets pose a deadly ingestion hazard to children.

    Product
    MiniWarGaming and Primal Horizon Disc Magnets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0512-2026·2026-05-15

    Sliced Deli Turkey Recalled Nationwide Over Listeria Risk

    Northfield Foods is recalling 187,000 lbs of sliced deli turkey after Listeria was found during routine testing.

    Product
    Northfield Select — Oven-Roasted Sliced Turkey Breast
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1935-2026·2026-05-13

    Aurous Centimeter Sizing Catheter Recalled for Marker Band Cracking Risk

    Cook Incorporated is recalling Aurous Centimeter Sizing Catheters due to risk of marker band cracking or breakage during angiographic procedures. Potential complications include device fragmentation, vessel injury, and in worst-case scenarios, life-threatening harm or death.

    Product
    Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 Sizing catheters are single-use, sterile catheters with gold marker bands. These catheters are for use in angiographic procedures and available in a variety of lengths (70 and 100 cm) and tip co
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1934-2026·2026-05-13

    Cook Centimeter Sizing Catheter recall due to marker band cracking

    Cook Incorporated is recalling Centimeter Sizing Catheters because marker bands may crack or break, potentially causing device fragmentation, vessel injury, or life-threatening harm.

    Product
    Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic procedures are available in a variety of French sizes, endhole sizes, lengths, materials and designs (e.g., polyethylene or nylon, non-braided or braided with 1:1 torque)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalCPSC·26465·2026-05-07

    EEMB Lithium Battery Packs Recalled for Unsafe Child-Resistant Packaging

    EEMB lithium coin battery packs sold online are not in child-resistant packaging as required by law. If swallowed by a child, these batteries can cause serious internal injuries or death.

    Product
    EEMB Lithium Battery Packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2031-2026·2026-05-06

    Insulin Pump Batteries Recalled After Sudden-Shutdown Reports

    OmniDose is recalling 23,000 lithium battery packs used in its X4 insulin pumps after reports of unexpected shutdown.

    Product
    Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: GENERAL KIT, Medline Kit Number/SKU DYNJ905664I
    Category
    Medical Device
    Distribution
    0 states
  • CriticalCPSC·26-184·2026-03-06

    Inclined Infant Nappers Recalled After Suffocation Reports

    Snuggle Loft has recalled 312,000 "Cradle Cloud" inclined infant nappers following 3 infant deaths reported over 5 years.

    Product
    Snuggle Loft — Cradle Cloud Inclined Infant Napper
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0633-2025·2025-03-19

    Ulker Biskrem Cocoa Biscuits Recalled for Undeclared Wheat and Egg

    ZB Importing LLC recalls Ulker Biskrem Cocoa Biscuits due to undeclared wheat and egg. Consumers with these allergies should not consume the product.

    Product
    Ulker Biskrem Cocoa Biscuit, item 8836, 10.6oz foil pack, 8 per case, UPC 8690504114628
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Food)·F-0609-2025·2025-03-19

    Aleppo Tahini Sesame Paste recalled due to Salmonella contamination

    Turkana Food Inc. is recalling Aleppo Tahini Sesame Paste because the product tested positive for Salmonella. The recalled product was distributed to 23 states.

    Product
    Aleppo Tahini Sesame Paste, 32oz, Plastic jar, 1lb (16oz), 12 per case
    Category
    Food
    Distribution
    23 states
  • CriticalFDA (Devices)·Z-1289-2025·2025-03-19

    Portex Endotracheal Tubes may deliver inadequate ventilation due to smaller diameter

    Portex Endotracheal Tubes from Smiths Medical ASD, Inc. may have a smaller diameter than expected, potentially causing inadequate ventilation and patient hypoxia.

    Product
    Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035 100/111/035 100/126/025 100/126/030 100/126/035 100/127/025 100/127/030 100/127/035 100/141/025 100/141/030 100/141/035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1257-2025·2025-03-12

    Insulin pump recall: Medtronic Paradigm models malfunction during airplane flight

    Medtronic MiniMed's Paradigm insulin pumps can malfunction during airplane flight due to air pressure changes, potentially causing dangerously high or low blood sugar levels that could be fatal.

    Product
    Paradigm insulin pump, REF: MMT-754
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1244-2025·2025-03-12

    Rotarex Atherectomy Catheter Recalled for Helix Fracture Risk

    Bard is recalling Rotarex Atherectomy System catheters due to potential helix fracture or breakage that could cause vessel injury and severe bleeding. Updated instructions are being distributed to clarify procedural steps to reduce this risk.

    Product
    Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF: 80237; S 8 F x 85 cm, REF: 80238; S 8 F x 110 cm, REF: 80239
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0588-2025·2025-03-12

    Watermelon and Cucumber Products Recalled for Potential Salmonella Contamination

    JFE Franchising is recalling watermelon and cucumber products with Tajin seasoning due to potential Salmonella contamination. Affected packages were distributed in TX, LA, WY, and AZ with sell-by dates from October 12 through December 5, 2024.

    Product
    Mixed Melon, Cucumber & Tajin 18 oz Watermelon & Cucumber w/ Tajin 18 oz packed in clamshells
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0578-2025·2025-03-05

    Gerber Baby Teething Sticks Recalled Due to Choking Risk

    Nestlé-USA is recalling all lots of Gerber Snacks for Baby Soothe 'n' Chew Teething Sticks in Strawberry Apple flavor following complaints of infant choking. The product was distributed across 42 states and Puerto Rico.

    Product
    Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER PRODUCTS CO., FREMONT, MI 49413
    Category
    Food
    Distribution
    45 states
  • CriticalCPSC·25157·2025-02-27

    Gas boilers recalled for carbon monoxide poisoning risk; two deaths reported

    Triangle Tube is recalling approximately 60,000 Prestige and Aerco Esteem gas boilers due to carbon monoxide release hazard. Two deaths and 25 CO leak incidents have been reported.

    Product
    Prestige Solo, Prestige Excellence, and Aerco Esteem condensing gas boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1144-2025·2025-02-26

    Allura Xper FD20 Fluoroscopy Table Mattress Issue Causes Fall Risk

    Philips recalls Allura Xper FD20 fluoroscopy patient tables due to a mattress issue that may cause patients to fall during procedures.

    Product
    Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1070-2025·2025-02-26

    Vascular Tack Endovascular System recalled for deployment and migration risks

    Spectranetics' Intact Vascular Tack Endovascular System may fail to deploy properly or migrate in blood vessels, potentially causing ischemia and requiring additional intervention.

    Product
    Intact Vascular Tack Endovascular System, to treat vascular dissections with Tack implant(s) following angioplasty: (4F,1.5-4.5mm), 150cm, REF: 154150041; Tack, 4F Gen 1.5, 150cm CE, REF: 154150042; Tack, 4F Gen 1.5, 90cm CE, REF: 154090042 (6F, 3.5 - 6.0mm), 135cm, REF: 15613
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1152-2025·2025-02-26

    Philips Allura Xper Patient Table Mattress Defect Fall Risk

    Philips is recalling the Allura Xper FD10C patient examination table due to a mattress defect that may allow patients to fall from the table. The device was distributed worldwide.

    Product
    Allura Xper FD10C; Catalog number: 722001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0211-2025·2025-02-05

    Prograf Tacrolimus Capsules Recall: Empty Capsules in Bottles

    Astellas Pharma recalls Prograf (tacrolimus) 0.5 mg capsules distributed nationwide due to empty capsules in bottles. Affected lot 0E3353D expires March 31, 2026.

    Product
    PROGRAF — PROGRAF (TACROLIMUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0428-2025·2025-02-05

    Lay's Classic Potato Chips recalled for undeclared milk allergen

    Frito Lay Inc. is recalling 6,344 bags of 13 oz. Lay's Classic Potato Chips distributed in Washington and Oregon due to an undeclared milk allergen that could cause allergic reactions.

    Product
    13 oz. Lay's Classic Potato Chips.
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0454-2025·2025-02-05

    Sushi Rolls Recalled Due to Possible Salmonella Contamination

    GBC Food Services (Yummi Sushi) has recalled multiple sushi roll products due to possible Salmonella contamination. The affected products were distributed in Texas and have best-by dates of 11/30/2024.

    Product
    Vegetarian Roll UPC: 85375900869 Qty: 1 Tray, Net Wt: 6.1oz (174g) 11/22 to 11/29/2024 Vegetarian Roll (Brown Rice) UPC: 85694200824 Qty: 1 Tray, Net Wt: 6.1oz (174g) 11/22 to 11/29/2024 Mixed Vegetable Roll (Brown Rice) UPC: 85694200880 Net Wt: 7.1oz (202g) 11/22 to 11/29/2024 V
    Category
    Food
    Distribution
    0 states