The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. 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.

16701–16725 of 29206

  • SevereFDA (Food)·F-1214-2017·2017-01-18

    All American Seasonings Recalls Triple Cheese Blend Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 59 bags of Triple Cheese Blend due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Triple Cheese Blend - No Color. Product Code: T4008. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1198-2017·2017-01-18

    All American Seasonings Recalls Buttermilk Ranch Seasoning for Salmonella Risk

    All American Seasonings, Inc. is recalling 26 boxes of Buttermilk Ranch Snack Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Buttermilk Ranch Snack Seasoning / Meat Chips. Product Code: T3760. 50 lb box
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1182-2017·2017-01-18

    FDA Recalls Broccoli Cheese Soup with Rice Due to Salmonella Risk

    Copperleaf Kitchen is recalling Country Gardens Cuisine Broccoli Cheese Soup with Rice after a supplier reported positive environmental tests for Salmonella.

    Product
    Country Gardens Cuisine, Singles, Broccoli Cheese Soup with Rice, Net Wt. 1.25 oz (35 grams)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1200-2017·2017-01-18

    All American Seasonings Recalls Kay's Naturals Cheese Puff Seasoning

    All American Seasonings is recalling 80 bags of Kay's Naturals Cheese Puff Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.

    Product
    Cheese Puff Seasoning / Kay's Naturals. Product Code: T3852. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1209-2017·2017-01-18

    All American Seasonings Recalls Spicy Nacho Seasoning Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 211 bags of 50 lb Spicy Nacho seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    Spicy Nacho. Product Code: T3552. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1227-2017·2017-01-18

    St. Clair Pistachio Cream Recalled for Salmonella Risk

    St. Clair Foods is recalling Pistachio Cream products due to potential salmonella contamination from an ingredient.

    Product
    Pistachio Cream, packaged under the following brands: (a) St. Clair, product code 104004, ST. CLAIR FOODS, INC., NET WT. 5 LBS (2.27 kg), MEMPHIS, TN 38116, UPC 7717114004 (b) Ron's Home Style Foods, product code 900603, NET WT. 5 LBS(2.27 kg), DIST. BY RON'S HOME STYLE FOODS…
    Category
    Food
    Distribution
    11 states
  • SevereNHTSA·17V037000·2017-01-17

    Highland Ridge RV Recalls 2017 Fifth Wheels and Travel Trailers for Gas Leak Risk

    Highland Ridge RV is recalling 2017 Open Range, Mesa Ridge, and Roamer models because the outside range can be stored with the gas valve open, creating a fire or explosion hazard.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW ROAMER, OPEN RANGE, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·005-2017·2017-01-14

    Olymel Recalls Pork Rib Tips Produced Without Federal Inspection

    Olymel S.E.C./L.P. is recalling pork rib tips shipped to Michigan restaurants because they were repacked and distributed without the benefit of federal inspection.

    Product
    Olymel S.E.C./L.P. Recalls Pork Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·17V034000·2017-01-13

    Renegade RV Recalls Motorhomes Due to Seat Belt Anchorage Defect

    REV Recreation Group is recalling specific Renegade RV motorhomes because seat belt anchorage hardware may pull out of the floor framing during a crash.

    Product
    RENEGADE RV — RENEGADE RV CORE, SPECIALTY SPRINTER, VIENNA, VILLAGIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·004-2017·2017-01-12

    Kettle Cuisine Recalls Chicken Soup for Misbranding and Undeclared Allergens

    Kettle Cuisine is recalling 3,096 pounds of chicken soup due to misbranding and undeclared allergens. The product was sold at Whole Foods in five states.

    Product
    Kettle Cuisine Midco, LLC — Kettle Cuisine, LLC Recalls Chicken Soup Product Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0366-2017·2017-01-11

    Wells Pharmacy Recalls Methylcobalamin Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling 265 vials of compounded Methylcobalamin 5,000 mcg/mL Injectable because the product lacks assurance of sterility.

    Product
    Methylcobalamin 5,000 mcg/mL Injectable, 10 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0345-2017·2017-01-11

    Wells Pharmacy Recalls Ceftazidime Ophthalmic Kits Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling 46 kits of compounded Ceftazidime Ophthalmic 2.25% due to a lack of assurance of sterility.

    Product
    Ceftazidime, Lyophilized, Ophthalmic 2.25% Kit, Rx only, Compounded by Wells Pharmacy, Ocala , FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0320-2017·2017-01-11

    Tri-Coast Pharmacy Recalls TriMix Injection Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 2 units of TriMix injection because the agency cannot assure the products are sterile.

    Product
    TriMix, Alprostadil/Phentolamine/Papaverine 100mcg/3mg/30mg/mL, (1 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0268-2017·2017-01-11

    Tri-Coast Pharmacy Recalls L-Tyrosine Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 50 vials of compounded L-Tyrosine 10 mg/mL because the products lack assurance of sterility.

    Product
    L-Tyrosine 10 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0421-2017·2017-01-11

    Wells Pharmacy Recalls Vitamin D3 Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling 335 vials of Vitamin D3 in Sesame Oil Injectable due to a lack of assurance of sterility.

    Product
    Vitamin D3 in Sesame Oil Injectable 50,000 IU/mL, 5 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0294-2017·2017-01-11

    Tri-Coast Pharmacy Recalls Sermorelin GT Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 920 vials of compounded Sermorelin GT nationwide due to a lack of assurance of sterility.

    Product
    Sermorelin GT (Sermorelin Acetate 15 mg/GHRP-2 5.4 mg/Theanine (L) 75 mg). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0266-2017·2017-01-11

    Tri-Coast Pharmacy Recalls L-Arginine HCL Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 41 vials of compounded L-Arginine HCL 100 mg/mL because there is a lack of assurance of sterility. The products were distributed nationwide.

    Product
    L-Arginine HCL 100 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0287-2017·2017-01-11

    Tri-Coast Pharmacy Recalls Sermorelin Acetate Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 260 vials of Sermorelin Acetate 6 mg compounded between May and November 2016 because the agency cannot assure the products are sterile.

    Product
    Sermorelin Acetate 6 mg. Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0418-2017·2017-01-11

    Wells Pharmacy Recalls Trimix Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling specific vials of Trimix Injectable because the agency could not ensure the product was sterile.

    Product
    Trimix Injectable 30 mg/3 mg/60 mcg/mL, a) 2 mL, b) 5 mL and c) 10 mL vials, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0299-2017·2017-01-11

    Tri-Coast Pharmacy Recalls Testosterone Cypionate Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 2,818 vials of compounded Testosterone Cypionate in Grapeseed nationwide due to a lack of assurance of sterility.

    Product
    Testosterone Cypionate in Grapeseed, 200 mg/mL, (5 ML and 10 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0376-2017·2017-01-11

    Wells Pharmacy Recalls Compounded Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling MIC+B12(M)+Carnitine injectable vials due to a lack of assurance of sterility. The recall covers 159 vials distributed nationwide.

    Product
    MIC+B12(M)+Carnitine 12.5 mg/50 mg/100 mg/1 mg/50 mg/mL Injectable, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide