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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1551–1575 of 89454

  • HighCPSC·26530·2026-06-04

    Boon NURSH 8 oz Reusable Baby Bottles Recalled for Choking Hazard

    TOMY International is recalling Boon NURSH 8 oz Reusable Baby Bottles because the hard plastic outer shell can bubble or peel, creating loose plastic pieces that pose a choking hazard to young children. No injuries have been reported.

    Product
    Boon NURSH 8 oz Reusable Baby Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26526·2026-06-04

    Children's Tiny Land Play Tents Recalled for Skin and Eye Irritation Risk

    Tiny Land Inc. is recalling about 7,500 children's play tents because fiberglass poles can shed fibers, causing skin and eye irritation. Consumers should stop using the tents immediately and contact Tiny Land for a free repair kit with plastic replacement poles.

    Product
    Children's Tiny Land Play Tents
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2234-2026·2026-06-03

    Medline Kits Containing Bupivacaine Hydrochloride Recalled Due to Quality and Efficacy Concerns

    Medline Industries, LP is recalling specific Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit SKU DYNJRA1181C; 2) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKu DYNJRA1860.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2235-2026·2026-06-03

    Medline Spinal Block Kits Recalled Due to Quality and Efficacy Concerns

    Medline Industries, LP is recalling Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BLOCK 22G QUINCKE 5S BU, Medline Kit SKU DYNJRA9026
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2236-2026·2026-06-03

    Medline spinal block trays recalled over Huons bupivacaine quality concerns

    Medline spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 30,120 kits are affected.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA1097; 2) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA1154; 3) SPINAL TRAY, Medline Kit SKU DYNJRA1192A; 4) BLOCK TRAY, Medline
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0852-2026·2026-06-03

    Giant Eagle pita chips made with recalled California Dairies milk powder

    Giant Eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps are being recalled because they were made with recalled California Dairies milk powder over Salmonella.

    Product
    giant eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps, Net Wt 7.33 oz. Shipping Case: 12 ct - 7.33 oz Bags Net Weight: 5.49 lbs. Legacy Bakehouse, LLC, Waukesha WI 53186.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2160-2026·2026-06-03

    RelayPro thoracic stent-graft clasp may not release from delivery system

    The RelayPro Thoracic Stent-Graft System is subject to a labeling update concerning proximal clasp disconnection from the outer control tube, which may prevent release of the graft.

    Product
    RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U 28-N4-32-164-28U 28-N4-32-164-32U 28-N4-32-209-28U 28-N4-32-209-32U 28-N4-32-259-32U 28-N4-34-109-34U 28-N4-34-154-30U 28-N4-34-154-34U 28-N4-34-209-30U 28-N4-34-209-34U 28-N4-34-259-34U 28-
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2233-2026·2026-06-03

    Medline spinal trays recalled over Huons bupivacaine quality concerns

    Medline spinal trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled over microbiology data integrity and efficacy complaints.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0245; 2) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0555; 3) SPINAL TRAY, Medline Kit SKU DYNJRA0836A; 4) SPINAL T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2232-2026·2026-06-03

    Medline pain and Whitacre spinal trays recalled over bupivacaine concerns

    Medline pain trays and Whitacre spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 28,106 kits are affected.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) PAIN TRAY, Medline Kit SKU DYNJRA1555; 2) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA1817; 3) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA1920; 4) ULTRASOUND
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0856-2026·2026-06-03

    Wawa diet lemon iced tea pints recalled over undeclared milk

    Wawa Diet Iced Tea Lemon in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 616 units are affected.

    Product
    Wawa Diet Iced Tea Lemon Pint (16oz),Plastic bottle
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·H-0858-2026·2026-06-03

    Wawa fruit punch pints recalled over undeclared milk allergen

    Wawa Fruit Punch in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 1,694 units are affected.

    Product
    Wawa Fruit Punch Pint (16oz), Plastic bottle
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-2237-2026·2026-06-03

    Medline spinal anesthesia trays recalled over Huons bupivacaine quality concerns

    Medline spinal anesthesia trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 200,702 kits are affected.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A; 2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B; 3) SPINAL PREP TRAY-LF, Medline Kit SKU DYNJRA0205B; 4) SPINAL TRAY, Medline Ki
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0857-2026·2026-06-03

    Wawa diet lemonade pints recalled over undeclared milk allergen

    Wawa Diet Lemonade in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 374 units are affected.

    Product
    Wawa Diet Lemonade Pint (16oz), Plastic bottle
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·H-0849-2026·2026-06-03

    Bulk banana smoothie base made with potentially Salmonella-contaminated ingredient

    A bulk banana smoothie base is being recalled because the firm received and used a potentially Salmonella-contaminated ingredient to manufacture various products. 4,980 pounds are affected.

    Product
    (BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2211-2026·2026-06-03

    Automated Impella Controllers await four pending hardware safety updates

    Automated Impella Controllers that have not been through Abiomed's servicing process are pending four hardware updates addressing motor control, startup and pump stop risks.

    Product
    Automated Impella Controller (AIC); Product Code: 0042-0000-US;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2231-2026·2026-06-03

    Medline anesthesia trays recalled over Huons bupivacaine quality concerns

    Medline anesthesia trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 1,100 kits are affected.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) ANESTHESIA TRAY, Medline SKU DYNJRA1355A; 2) SPINAL ANESTHESIA TRAY, Medline SKU DYNJRA2151.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0850-2026·2026-06-03

    Legacy Bakehouse butter parsley bagel crisps made with recalled milk powder

    Butter Parsley Bagel Crisps from Legacy Bakehouse are being recalled because they were made with recalled California Dairies milk powder over Salmonella.

    Product
    Butter Parsley Bagel Crisps, Item Number 18490, Net Weight: 10 lbs. Legacy Bakehouse, LLC, N8W22100 Johnson Dr., Waukesha, WI 53166.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2238-2026·2026-06-03

    Automated Impella Controllers recalled over alarm, power and purge cassette faults

    Automated Impella Controllers sold outside the US are being recalled over alarm failures, power-path faults, electrical-short risks, inaccurate motor-current sensing and purge cassette misalignment.

    Product
    Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 3. Impella Controller, Packaged, UK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0851-2026·2026-06-03

    Legacy Bakehouse parmesan herb bagel crisps made with recalled milk powder

    Parmesan & Herb Bagel Crisps from Legacy Bakehouse are being recalled because they were made with recalled California Dairies milk powder over Salmonella.

    Product
    Parmesan & Herb Bagel Crisps, Item Number 18139, Net Weight: 10 lbs. Legacy Bakehouse, LLC, N8W22100 Johnson Dr., Waukesha, WI 53166.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-2258-2026·2026-06-03

    Philips Azurion system hard drives may degrade and lose imaging

    Philips Azurion interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.

    Product
    Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225), Azurion 7 B20 (722068, 722226), Azurion 7 M12 (722078, 722223), Azurion 7 M20 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2230-2026·2026-06-03

    Halyard nitrile exam gloves failed chemical permeation performance specifications

    Halyard Purezero Ultraviolet Nitrile Exam Gloves are being recalled because they failed to meet specifications for chemical permeation performance. 452,500 units are affected.

    Product
    Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2247-2026·2026-06-03

    GE ApexPro v6.0 software may lose ECG and SpO2 monitoring

    GE HealthCare ApexPro v6.0 eDelivery Software is being recalled because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.

    Product
    GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2239-2026·2026-06-03

    HydroMARK breast biopsy markers may carry the wrong inner labeling

    HydroMARK Breast Biopsy Site Markers are being recalled because boxes labeled as T3 markers may contain individual packages labeled as T4 markers. 1,910 units are affected.

    Product
    HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3
    Category
    Medical Device
    Distribution
    Distributed nationwide