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.

22676–22700 of 32171

  • SevereFDA (Food)·F-1489-2015·2015-07-08

    Snoqualmie Apple Cider Sorbet Recalled for Listeria Risk

    Snoqualmie Gourmet Ice Cream is recalling Apple Cider Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 3-gallon tubs.

    Product
    Apple Cider Sorbet, sold under Snoqualmie brand. Product is sold in 3 gallon plastic tubs. No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1165-2015·2015-07-08

    Lincare Recalls TPN 3:1 Bags Due to Sterility Concerns

    Lincare, Inc. is recalling TPN 3:1 bags compounded in May 2015 because the sterility of the product is not assured.

    Product
    TPN 3:1, 1844 mL Bags, Qty: 6, Base Formula Sodium Chloride, Dextrose 70%, Clinisol SF 15%, Intralipid 20%, Water for Inj; Electrolytes KCL, Ca Gluconate, MgSO4, K Phos; Vitamins, trace elements and medications Multitrace-4, Multi Vitamin, Rx Only. Compounded by: United Medical…
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1459-2015·2015-07-08

    Snoqualmie Ice Cream Mix Recalled for Potential Listeria Contamination

    Snoqualmie Gourmet Ice Cream is recalling 14% Ice Cream Mix due to potential Listeria monocytogenes contamination.

    Product
    14% Ice Cream Mix with acme stabilizer, sold under Snoqualmie brand. Product is sold in 2.5 gallon clear flexible plastic bags. No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1873-2015·2015-07-08

    Palindrome Precision SI Chronic Catheter Kit Recalled for Antimicrobial Failure

    Covidien LLC is recalling Palindrome Precision SI Chronic Catheter Kits because they may not meet antimicrobial specifications.

    Product
    Palindrome Precision SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 28cm Item Code: 8888145064CP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1566-2015·2015-07-08

    Snoqualmie Pistachio Gelato Recalled for Listeria Contamination Risk

    Snoqualmie Gourmet Ice Cream is recalling Pistachio Gelato due to potential Listeria monocytogenes contamination. The product was distributed nationwide in various container sizes.

    Product
    Pistachio Gelato, sold under Snoqualmie Ice Cream brand. Product is sold in 1 gallon plastic trays; 1.5 and 3 gallon plastic tubs and other unknown container type/sizes. No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1173-2015·2015-07-08

    Lincare Recalls Ceftriaxone Sodium IV Bags Due to Sterility Concerns

    Lincare, Inc. is recalling Ceftriaxone Sodium IV bags because the sterility of the product is not assured. The affected units were distributed in Arkansas.

    Product
    CEFTRIAXONE SODIUM 2000mg / NS 50mL, Qty:4 50 mL Bags, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1567-2015·2015-07-08

    Snoqualmie Pumpkin Gelato Recalled for Potential Listeria Contamination

    Snoqualmie Gourmet Ice Cream is recalling Pumpkin Gelato due to the potential for Listeria monocytogenes contamination. The product was distributed nationwide in 3-gallon tubs.

    Product
    Pumpkin Gelato, sold under Snoqualmie Ice Cream brand. Product is sold in 3 gallon plastic tubs. No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1494-2015·2015-07-08

    Snoqualmie Berry Sorbet Recalled for Potential Listeria Contamination

    Snoqualmie Gourmet Ice Cream is recalling Berry Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 1-gallon trays.

    Product
    Berry Sorbet, sold under Snoqualmie brand. Product is sold in 1 gallon plastic trays. No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2786-2015·2015-07-08

    Walgreens Recalls Nice! Powdered Sugar Mini Donuts Due to Mold

    Walgreens is recalling Nice! Powdered Sugar Mini Donuts because they may contain mold. Alleged illnesses have been reported in connection with this product.

    Product
    Nice! Powdered Sugar Mini Donuts 11.5 oz packaged in a white and pink box with with pink and black lettering.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1472-2015·2015-07-08

    Snoqualmie Cookie Dough Custard Recalled for Listeria Risk

    Snoqualmie Gourmet Ice Cream is recalling Cookie Dough Custard due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 3-gallon tubs.

    Product
    Cookie Dough Custard, sold under Snoqualmie brand. Product is sold in 3 gallon plastic tubs. No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1180-2015·2015-07-08

    Lincare Recalls Fluorouracil IV Bags Due to Sterility Concerns

    Lincare, Inc. is recalling Fluorouracil IV bags compounded by United Medical IV Center because the sterility of the product is not assured.

    Product
    Fluorouracil 4600mg / D5W 292 mL, Qty: 1 292 mL Bag, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1199-2015·2015-07-08

    Lincare Recalls Cefepime HCl IV Bags Due to Sterility Concerns

    Lincare, Inc. is recalling Cefepime HCl IV bags compounded by United Medical IV Center because the sterility of the product is not assured.

    Product
    Cefepime HCl, CEFEPIME 850 mg NS 50mL AccuFlo, Qty: 12 50 mL Bags, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·15V435000·2015-07-08

    Ditch Witch T14MV Trailer Recall for Brake Wiring Defect

    Charles Machine Works is recalling 2014-2015 Ditch Witch T14MV trailers due to a wiring defect that may prevent brakes from applying during a breakaway.

    Product
    DITCH WITCH — DITCH WITCH T14MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1892-2015·2015-07-08

    Palindrome HSI Chronic Catheter Kit Recalled for Antimicrobial Specification Failure

    Covidien LLC is recalling Palindrome HSI Chronic Catheter Kits because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 internationally.

    Product
    Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 28cm Item Code: 8888145049
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1194-2015·2015-07-08

    Lincare Recalls Pfizerpen-G IV Bags Due to Sterility Concerns

    Lincare, Inc. is recalling Pfizerpen-G IV bags compounded by United Medical IV Center because the sterility of the product is not assured.

    Product
    Pfizerpen-G 4.2 MU / SW 240 mL AccuFlo, Packaged in 2 240 mL Bags, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1954-2015·2015-07-08

    ViewRay Treatment Planning Software Recalled for Location Calculation Failure

    ViewRay is recalling Treatment Planning and Delivery System Software version 3.6 because it fails to determine new patient locations if imaging is not enabled.

    Product
    Treatment Planning and Delivery System Software version 3.6. ViewRay. Indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated.
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Drugs)·D-1157-2015·2015-07-08

    Lincare Recalls TPN 3:1 Bags Due to Sterility Concerns

    Lincare, Inc. is recalling TPN 3:1 bags compounded by United Medical IV Center because the sterility of the product is not assured.

    Product
    TPN 3:1, 1800 ml Bags, Qty: 2, Base Formula NaCl 0.9%, Dextrose 70%, Travasol 10%, Intralipid 20%, Water; Electrolytes K Phos, Mag Sulfate, KCL, Ca Gluconate; Vitamins, trace elements and medications Multitrace-4, Multi Vitamin, Rx Only. Compounded by: United Medical IV Center…
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1497-2015·2015-07-08

    Snoqualmie Blood Orange Sorbet Recalled for Listeria Risk

    Snoqualmie Gourmet Ice Cream is recalling Blood Orange Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 3-gallon tubs.

    Product
    Blood Orange Sorbet, sold under Snoqualmie brand. Product is sold in 3 gallon plastic tubs. No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1181-2015·2015-07-08

    Lincare Recalls Vancomycin Syringes Due to Sterility Assurance Concerns

    Lincare, Inc. is recalling Vancomycin HCL 250mg syringes compounded by United Medical IV Center in Arkansas because the sterility of the product is not assured.

    Product
    VANCOMYCIN HCL 250mg / NS 6mL syringe, Packaged in 6 mL Syringes, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·15V431000·2015-07-07

    Dodge Journey Recall: Engine Cover May Detach and Cause Fire

    Chrysler is recalling 2011-2015 Dodge Journey vehicles because the engine cover may detach and contact the exhaust manifold, increasing the risk of a vehicle fire.

    Product
    DODGE — DODGE JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·098-2015·2015-07-07

    Bassett and Walker Recalls Beef Lips Lacking Import Inspection

    Bassett & Walker International is recalling approximately 1,540 pounds of beef lip products produced in Australia that were not inspected at the U.S. point of entry.

    Product
    Bassett and Walker International, Inc. Recall Beef Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V429000·2015-07-06

    Entegra Recalls 2015-2016 Cornerstone Motorhomes Due to Brake Hose Rubbing

    Entegra is recalling 2015-2016 Cornerstone motorhomes because rear jack plates may rub against the brake air hose, potentially reducing braking performance and increasing crash risk.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V428000·2015-07-06

    Prevost Recalls 2015 X3-45 Coaches Due to Front Hub Carrier Defect

    Prevost is recalling 68 model year 2015 X3-45 Commuter Coaches because front hub carriers may leak or crack, potentially causing loss of vehicle control.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·097-2015·2015-07-03

    Lombardi Brothers Meats Recalls Beef Products Due To E. Coli O157:H7

    Lombardi Brothers Meats is recalling approximately 26,975 pounds of steak and ground beef products due to possible E. coli O157:H7 contamination.

    Product
    Lombardi Brothers Meats Recalls Steak and Ground Beef Products Due To Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    4 states