The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

3176–3200 of 4878

  • SevereFDA (Food)·F-0091-2023·2022-11-09

    Chocolate Banana Babies Recalled for Undeclared Peanut Allergen

    Diana's Milk Chocolate Banana Babies are recalled due to undeclared peanut allergen. About 18,468 retail units distributed in UT, MI, IA, WA, and CA are affected.

    Product
    Diana s Milk Chocolate Banana Babies UPC: 7-43490-00010-4 10.5-ounce 5 count packages
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0107-2023·2022-11-09

    Brie Cheese Recalled for Potential Listeria Contamination

    Old Europe Cheese is recalling TASTE OF INSPIRATION 8 oz Brie cheese rounds due to potential Listeria monocytogenes contamination. The product was distributed across multiple states and Mexico.

    Product
    TASTE OF INSPIRATION 8 oz Brie - w/Herb center layer, rounds UPC 725439802567
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Food)·F-0084-2023·2022-11-09

    Halibut Fillets and Portions Recalled for Possible Salmonella Contamination

    Mariscos Bahia Inc recalls halibut fillets and portions due to possible salmonella contamination. Affected product was distributed to 179 restaurant customers in Arizona and California.

    Product
    Halibut (fillets and portions) packed in 10-50 lb. corrugated cardboard or Styrofoam boxes
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0112-2023·2022-11-09

    Baked Brie Cheese Recalled for Potential Listeria Contamination

    Old Europe Cheese is recalling LA BONNE VIE and Reny Picot brand Cranberry Baked Brie cheese due to potential Listeria monocytogenes contamination.

    Product
    LA BONNE VIE 11 oz Cranberry Baked Brie UPC 820581678821; Reny Picot 11 oz Cranberry Baked Brie UPC 033421051115
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Food)·F-0113-2023·2022-11-09

    Reny Picot Apple Baked Brie recalled for potential Listeria contamination

    Old Europe Cheese, Inc. is recalling Reny Picot Apple Baked Brie due to potential Listeria monocytogenes contamination. The recall affects 1,309 pieces with best-by dates from September 28, 2022 to December 14, 2022.

    Product
    Reny Picot 11 oz Apple Baked Brie UPC 033421500811
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Devices)·Z-0143-2023·2022-11-09

    Hillrom WatchCare Incontinence System Recalled for Radio Frequency Interference

    Baxter Healthcare recalls the Hillrom WatchCare Incontinence Management System for Progressa Bed due to potential radio frequency emissions that may interfere with other medical devices including telemetry monitors and infusion pumps.

    Product
    Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Progressa Bed, Product Code/Part Number P00697903.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0142-2023·2022-11-09

    Hillrom WatchCare Incontinence System recalled for radio frequency interference risk

    Baxter Healthcare is recalling the Hillrom WatchCare Incontinence Management System due to radio frequency emissions that may interfere with other critical medical devices including insulin pumps and fetal monitors.

    Product
    Hillrom Hospital Bed Accessory, Watch Care Incontinence Management System for Centrella Bed, Product Code/Part Number P00697905
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0083-2023·2022-11-09

    Fresh Salmon Fillets Recalled Due to Salmonella Contamination Risk

    Mariscos Bahia Inc is recalling fresh salmon fillets due to possible salmonella contamination. The product was distributed to restaurants in Arizona and California.

    Product
    Fresh Salmon fillets packed in 10-50 lb. corrugated cardboard or Styrofoam boxes
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0085-2023·2022-11-09

    Chilean Seabass Fillets Recalled for Possible Salmonella Contamination

    Mariscos Bahia Inc is recalling Chilean Seabass fillets and portions due to possible salmonella contamination. The product was distributed to restaurants in Arizona and California.

    Product
    Chilean Seabass (fillets and portions) packed in 10-50 lb. corrugated cardboard or Styrofoam boxes
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0144-2023·2022-11-09

    Hillrom WatchCare Incontinence System Recalled for Radio Frequency Interference

    Baxter Healthcare recalls the Hillrom WatchCare Incontinence Management System (63 units in US) because radio frequency emissions from the device may interfere with other medical equipment including infusion pumps and insulin pumps.

    Product
    Hillrom Hospital Bed Accessory, WatchCare Incontinence Management System for VersaCare Bed Rev. K, Product Code/Part Number P00697902
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·22V143000·2022-11-03

    Forest River 2022 Travel Trailers Recalled for Coupler Weld Defect

    Forest River is recalling certain 2022 travel trailers due to improperly welded couplers that may cause trailer separation from the tow vehicle. Dealers will replace the coupler at no charge.

    Product
    FOREST RIVER — 2022 FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23034·2022-11-03

    BLACK+DECKER Garment Steamers Recalled for Burn Hazard from Hot Water

    Empower Brands recalls about 518,500 BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, posing a burn hazard. The company has received 241 reports of hot water expelling, including 32 reports of burn injuries.

    Product
    BLACK+DECKER Model HGS011 Easy Garment Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0117-2023·2022-11-02

    Caribou Coffee Snack Fruit and Cheese Plate Recalled for Listeria Risk

    Cut Fruit Express is recalling Caribou Coffee Snack Fruit and Cheese Plates due to potential Listeria in the Brie cheese. Affected units were distributed in Minnesota with Use By dates from September 30 to October 9, 2022.

    Product
    Caribou Coffee Snack Fruit and Cheese Plate, item # 3818, Net Wt 6.2 oz. (176g) 3 cheeses, red grapes, apples, rosemary crackers. Keep Refrigerated. Manufactured By: Cut Fruit Express, Inver Grove Heights, MN
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0141-2023·2022-11-02

    Earth Grown Vegan Falafel Recalled for E. Coli Contamination

    Earth Grown Vegan Garlic & Herb Falafel is being recalled due to possible contamination with Shiga toxin-producing E. coli. The recall affects over 190,000 units distributed across multiple US states.

    Product
    Earth Grown Vegan Garlic & Herb Falafel NET WT 12 OZ (340g), 12 pieces UPC:4 0991002 24344
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Drugs)·D-0022-2023·2022-11-02

    Sodium Bicarbonate Injection Recalled for Defective Vials with Glass Breakage Risk

    Exela Pharma Sciences is recalling 2,123,040 vials of Sodium Bicarbonate 8.4% Injection due to container defects causing vial breakage and glass release when pressurized during product preparation.

    Product
    SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0023-2023·2022-11-02

    Sodium Bicarbonate Injection Recalled for Defective Vials and Glass Breakage

    Nationwide recall of 8.4% sodium bicarbonate injection vials due to container defects causing vial breakage and glass fragments when pressurized during preparation.

    Product
    8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd for: Civica, Inc. Lehi, Utah 84043, Mfd by: Exela Pharma Sciences, LLC, Lenoir, NC 28645, Carton NDC 72572-740-20, vial NDC 72572-740-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0019-2023·2022-11-02

    Atenolol 25mg bottles mislabeled; contain Clopidogrel 75mg tablets

    Golden State Medical Supply Inc. is recalling 2,584 bottles of Atenolol 25mg tablets nationwide. Bottles labeled as Atenolol 25mg actually contain Clopidogrel 75mg tablets—a different medication.

    Product
    ATENOLOL — ATENOLOL (ATENOLOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0140-2023·2022-11-02

    Earth Grown Vegan Falafel Recalled for Possible E. coli Contamination

    Earth Grown Vegan Traditional Falafel is being recalled due to possible contamination with Shiga toxin-producing E. coli. The FDA Class I recall affects approximately 190,860 units distributed across multiple U.S. states.

    Product
    Earth Grown Vegan Traditional Falafel NET WT 12 OZ (340g), 12 pieces UPC:4 0991002 24337
    Category
    Food
    Distribution
    18 states
  • SevereCPSC·23705·2022-10-27

    LG Energy Solution RESU 10H Batteries Recalled for Fire Hazard

    LG Energy Solution is recalling about 11,500 RESU 10H lithium-ion residential energy storage batteries because they can overheat and pose a fire risk with harmful smoke emissions. One incident of smoking and fire with property damage has been reported.

    Product
    LG Energy Solution "RESU 10H" Lithium-Ion Residential Energy Storage System Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23026·2022-10-27

    Horizon T101-05 Treadmills Recalled for Unexpected Speed and Stop Hazard

    Horizon T101-05 folding treadmills can unexpectedly accelerate, change speed, or stop without user input, posing a fall hazard. About 192,000 units sold in the U.S. are affected; 71 injuries including broken bones have been reported.

    Product
    Horizon T101-05 Treadmills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0075-2023·2022-10-26

    Iso-Gard Filter S Medical Gas Filters Recalled Due to Device Splitting Risk

    TELEFLEX is recalling 355 units of Iso-Gard Filter S medical gas filters nationwide due to incidents of device splitting or detaching during use. The FDA classified this as a Class I recall.

    Product
    Iso-Gard Filter S, with Expandi-Flex, Tethered Cap, REF: a) 19261T, OUS only; b) 19262T, OUS only; c) 19272T, OUS only; Microbial medical gas filter, single-use,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0074-2023·2022-10-26

    Medical Gas Filter Devices Recalled Due to Splitting and Detachment Risk

    Teleflex is recalling Iso-Gard Filter S microbial medical gas filters that may split or detach during use. The recall affects 164 units distributed nationwide.

    Product
    Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical gas filter, single-use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0038-2023·2022-10-26

    Dark Chocolate Almonds recalled for undeclared milk allergen

    Dark Chocolate Almonds sold at Safeway, Albertsons, and Roths Fresh Market contain undeclared milk allergen. The FDA Class I recall affects 1,701 cases distributed in Oregon and Washington.

    Product
    Dark Chocolate Almonds distributed to Safeway/Albertsons is packaged in a clear clamshell container with a top label that displays PRODUCE Dark Chocolate Almonds , net weight of 9.5 oz., UPC 0 19061 19371 2. Distributed by Rivertrail Foods with an address of 4660 Ridge Dr. NE. S
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0080-2023·2022-10-26

    Fenugreek dietary supplement recalled for potential Salmonella contamination

    Best Nutritionals LLC is recalling Best Naturals Fenugreek 610mg capsules due to potential Salmonella contamination. The product was distributed online via internet sellers and FBA.

    Product
    White plastic bottle with green, gold, and blue labeling containing 360, 610mg hard gelatin capsules of Fenugreek seed powder, labeled in part, "Best Naturals Fenugreek Premium Herbal 610mg 3rd Party Lab Tested 360 CAPSULES DIETARY SUPPLEMENT", best by 10/24, lot 102120
    Category
    Food
    Distribution
    0 states