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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8901–8925 of 114917

  • HighFDA (Food)·H-0351-2025·2025-08-06

    Fresh Scottish salmon fillets processed under insanitary conditions in Georgia

    Fresh Scottish Salmon Fillets sold in 50 lb boxes are being recalled because ready-to-eat fish was processed under insanitary conditions, as notified by the Georgia Department of Agriculture.

    Product
    Fresh Scottish Salmon Fillet, Net WT (variable weight) 50 lb brown corrugated carboard box (up to 6 fillets per box). Boxes contain ice for temperature control. Keep Refrigerated.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2233-2025·2025-08-06

    LVP blood administration sets have potential for external cassette leaks

    LVP Blood Products Administration Sets are being recalled because of the potential for external cassette leaks. 14,280 units are affected.

    Product
    LVP Blood Products Administration Set Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter (Qty 20). Product Code: SET-0014-20.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0371-2025·2025-08-06

    Reisman's cinnamon wrap recalled over undeclared wheat and soy

    Reisman's Cinnamon Wrap 3 oz is being recalled because of undeclared wheat and soy. The action covers 186,582 units across all recalled Reisman's products.

    Product
    Reisman's Cinnamon Wrap 3 oz.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0357-2025·2025-08-06

    Reisman's jumbo black and white cookies recalled over undeclared wheat

    Reisman's Jumbo Black & White Cookies 3 oz are being recalled because of undeclared wheat. The action covers 186,582 units across all recalled Reisman's products.

    Product
    Reisman's Jumbo Black & White Cookies 3 oz.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2189-2025·2025-08-06

    Philips Allura R8.2.x systems may temporarily lose x-ray imaging functionality

    Philips Allura R8.2.x systems are being recalled because of the potential for temporary loss of imaging (X-ray) functionality due to a software issue. 4,508 units are affected.

    Product
    Philips Allura R8.2.x Systems. Software Verion: R8.2.x. 1. Allura Xper FD10, Model Number: 722026. 2. Allura Xper FD10/10, Model Number: 722027. 3. Allura Xper FD20, Model Number: 722028. 4. Allura Xper FD20/10, Model Number: 722029. 5. Allura Xper FD10 OR Table…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0349-2025·2025-08-06

    Casa Mamita churro bites recalled after cheese stick found in bag

    Casa Mamita Churro Bites Filled with Chocolate Hazelnut Cream are being recalled for undeclared milk after a consumer found a breaded halloumi cheese stick in a bag. 19,080 sell units affected.

    Product
    Casa Mamita, Churro Bites Filled with Chocolate Hazelnut Cream, 7.5 oz , Cardboard Box, 12 boxes per case, Keep Frozen Until Ready For Use
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2223-2025·2025-08-06

    Blood agar plates may carry Listeria monocytogenes surface contamination

    Blood Agar with 5% Sheep Blood, product number R01202, is being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 1,552 units affected.

    Product
    Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2175-2025·2025-08-06

    Inseego dongle kit flash drives carry outdated patient monitor software

    Inseego USB8 4G Dongle Kits for the Tempus Pro Monitor are being recalled because the kit's USB flash drive contains outdated software that could revert the monitor and reintroduce a previous issue. 55 units affected.

    Product
    Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an accessory to the Tempus Pro Monitor, REF: 00-1007-R, 00-1024-R, 00-1026-R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0377-2025·2025-08-06

    Reisman's cinnamon babka slices recalled over undeclared wheat and soy

    Reisman's Cinnamon Babka Slices 3 oz are being recalled because of undeclared wheat and soy. The action covers 186,582 units across all recalled Reisman's products.

    Product
    Reisman's Cinnamon Babka Slices 3 oz.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2217-2025·2025-08-06

    SmartPath to Ingenia Elition X gradient coils may overheat

    SmartPath to Ingenia Elition X systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 33 units affected.

    Product
    SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118, (2) 782144;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2208-2025·2025-08-06

    Philips Ingenia Ambition S gradient coils may act as heat source

    Ingenia Ambition S MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 611 units are affected.

    Product
    Ingenia Ambition S Model Numbers (REF): (1) 781359, (2) 782108, (3) 782133 (China ONLY), (4) 782139;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2207-2025·2025-08-06

    Philips Ingenia 3.0T CX gradient coils may act as heat source

    Ingenia 3.0T CX MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 350 units are affected.

    Product
    Ingenia 3.0T CX Model Numbers (REF): (1) 781271, (2) 782105;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0373-2025·2025-08-06

    Reisman's chocolate flaky wrap recalled over undeclared wheat and soy

    Reisman's Chocolate Flaky Wrap 3 oz is being recalled because of undeclared wheat and soy. The action covers 186,582 units across all recalled Reisman's products.

    Product
    Reisman's Chocolate Flaky Wrap 3 oz.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0356-2025·2025-08-06

    Reisman's jumbo chocolate chip cookies recalled over undeclared wheat

    Reisman's Jumbo Chocolate Chip Cookies 3 oz are being recalled because of undeclared wheat. The action covers 186,582 units across all recalled Reisman's products.

    Product
    Reisman's Jumbo Chocolate Chip Cookies 3 oz.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0375-2025·2025-08-06

    Reisman's soft chip cookie two-packs recalled over undeclared wheat

    Reisman's 2/pk Soft Chip Cookie with fudge filling, 3 oz, is being recalled because of undeclared wheat. The action covers 186,582 units across all recalled Reisman's products.

    Product
    Reisman's 2/pk Soft Chip Cookie (with fudge filling) 3 oz.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Drugs)·D-0545-2025·2025-08-06

    Bicillin L-A 2.4 million unit vials recalled after particulates found

    Bicillin L-A (penicillin G benzathine injectable suspension) 2,400,000 units per 4 mL is being recalled because of CGMP deviations, with particulates identified during visual inspection. 19,279 vials affected.

    Product
    BICILLIN L-A — BICILLIN L-A (PENICILLIN G BENZATHINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0376-2025·2025-08-06

    Reisman's chocolate babka slices recalled over undeclared wheat and soy

    Reisman's Chocolate Babka Slices 3 oz are being recalled because of undeclared wheat and soy. The action covers 186,582 units across all recalled Reisman's products.

    Product
    Reisman's Chocolate Babka Slices 3 oz.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·H-0361-2025·2025-08-06

    Reisman's cappuccino bars recalled over undeclared wheat and soy

    Reisman's Cappuccino Bars 3 oz are being recalled because of undeclared wheat and soy. The action covers 186,582 units across all recalled Reisman's products.

    Product
    Reisman's Cappuccino Bars 3 oz.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-2199-2025·2025-08-06

    SwabFlush prefilled syringes carry SwabCaps with a compromised seal

    SwabFlush Prefilled Syringes with ICU Medical SwabCaps are being recalled because a manufacturing issue affects the SwabCap seal, which may reduce disinfection of the luer access valve. 1,427,100 units affected.

    Product
    SwabFlush Prefilled Syringe with ICU Medical SwabCaps, 10mL Model no. EMZE010301
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2211-2025·2025-08-06

    Philips Ingenia Elition X gradient coils may act as heat source

    Ingenia Elition X MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 632 units are affected.

    Product
    Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136, (5) 782151 (China ONLY);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0544-2025·2025-08-06

    Bicillin L-A penicillin vials recalled after particulates found during visual inspection

    Bicillin L-A (penicillin G benzathine injectable suspension) 1,200,000 units per 2 mL is being recalled because of CGMP deviations, with particulates identified during visual inspection. 50,855 vials affected.

    Product
    BICILLIN L-A — BICILLIN L-A (PENICILLIN G BENZATHINE)
    Category
    Drug
    Distribution
    Distributed nationwide