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.

11701–11725 of 29163

  • SevereFDA (Food)·F-1569-2019·2019-07-24

    ADM Recalls H&R Flour Due to Potential E. coli O26 Presence

    ADM is recalling H&R Flour 50lb bags due to potential E. coli O26 presence. The product was distributed to retailers and food service locations in multiple states.

    Product
    H&R Flour (Hotel and Restaurant) 50lb bags Product Codes 706220
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1558-2019·2019-07-24

    Perrigo Recalls Parent's Choice Infant Formula Due to Metal Fragments

    Perrigo Company PLC is recalling specific lots of Parent's Choice Advantage Infant Formula because the product may contain metal fragments.

    Product
    Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron, 35 oz, 922 g, with UPC: 078742022468
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1977-2019·2019-07-24

    FDA Recalls Advincula Delineator Uterine Manipulator Due to Cracking Risk

    CooperSurgical is recalling 213 units of the Advincula Delineator Uterine Manipulator because the soft cup may crack during use, posing a risk of lacerations.

    Product
    Advincula Delineator with Ultem Plastic Soft Cup size 2.5 cm; Part No. AD750SC-KE25 The Advincula Delineator Uterine Manipulator is a single-use disposable device designed specifically for Total Laparoscopic Hysterectomy (TLH), Laparoscopic Assisted Vaginal Hysterectomy…
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Food)·F-1554-2019·2019-07-24

    Sprouts Organic Cut Leaf Spinach Recalled for Listeria

    Sprouts Farmers Market is recalling Organic Cut Leaf Spinach because testing revealed the presence of Listeria monocytogenes.

    Product
    Sprouts Farmers Market Organic Cut Leaf Spinach, Net Wt 16 Oz (1 lb), 453 g, Manufactured exclusively for Sprouts Farmers Market, Phoenix, AZ UPC 8 74875 00991 4, packaged in plastic bags, 12 bags per case.
    Category
    Food
    Distribution
    19 states
  • SevereFDA (Food)·F-1570-2019·2019-07-24

    ADM Recalls Dellalo HG Pizza Flour Due to Potential E. coli O26

    ADM is recalling Dellalo HG Pizza Flour 50lb bags due to the potential presence of E. coli O26. The product was distributed in Pennsylvania.

    Product
    Dellalo HG Pizza Flour 50lb bags Product Code 845212 Lot#: 8344BF
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1568-2019·2019-07-24

    ADM Recalls Gigantic Flour Due to Potential E. coli O26 Presence

    ADM is recalling Gigantic Flour 50lbs (Lot 8346BF) due to the potential presence of E. coli O26. The product was distributed to various retailers and commercial bakeries.

    Product
    Gigantic Flour 50lbs Product Code 701220 Lot #: 8346BF
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1576-2019·2019-07-24

    Commander Flour Bl is recalled due to potential E. coli O26 contamination

    A flour product (Commander Flour Bl, Product Code 704060) manufactured by ADM Chicago is being recalled because there is a potential presence of E. coli O26.

    Product
    Commander Flour Bl, En, Br, Mt Product Code 704060
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1943-2019·2019-07-24

    Datascope CS300 Intra-Aortic Balloon Pump Recalled for Battery Maintenance Issues

    Datascope Corp. is recalling CS300 Intra-Aortic Balloon Pumps because improper battery maintenance may result in less than minimum run time.

    Product
    CS300 Intra-Aortic Balloon Pump, English, 110V; 0998-00-3023-53 For cardiovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1580-2019·2019-07-24

    ADM Recalls Gold Medal Flour Due to Potential E. coli O26 Presence

    ADM is recalling Gold Medal Flour Mt Bulk Product Code 805046 due to the potential presence of E. coli O26. The product was distributed to commercial bakeries and food service operators.

    Product
    Gold Medal Flour Mt Bulk Product Code 805046
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1768-2019·2019-07-24

    CareFusion Recalls Alaris Pump Model 8100 Due to Bezel Plastic Weakening

    CareFusion is recalling Alaris Pump Model 8100 units manufactured between April 2011 and June 2017 because the bezel plastic may weaken, potentially causing infusion errors.

    Product
    Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. The following products are affected by this recall as they are pumps or pump assemblies with bezels manufactured between April 2011 and June 2017 with the FR-110 plastic.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1556-2019·2019-07-24

    Weaver Popcorn Recalls Cheddar Popcorn Due to Salmonella Concern

    Weaver Popcorn Co. is recalling specific lots of cheddar popcorn due to a concern of possible Salmonella contamination.

    Product
    Cheddar popcorn, bulk, packaged in metalized film, Net Wt. 4.85 lbs., Item No. 107065
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1942-2019·2019-07-24

    Datascope CS100 Intra-Aortic Balloon Pump Recalled for Battery Maintenance Issues

    Datascope Corp. is recalling CS100 Intra-Aortic Balloon Pumps because improper battery maintenance may result in less than the minimum run time of operating power.

    Product
    CS100 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3013-55 For cardiovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V544000·2019-07-24

    Toyota and Lexus Recall Vehicles for Brake Booster Pump Failure

    Toyota is recalling specific 2019-2020 hybrid and luxury vehicles because a brake booster pump failure may disable stability control and braking assist.

    Product
    TOYOTA — TOYOTA, LEXUS RAV4 HYBRID, UX HYBRID, LC500, PRIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1563-2019·2019-07-24

    ADM Recalls Bulk Gold Medal Flour Due to Potential E. coli O26

    ADM is recalling 191,000 pounds of bulk Gold Medal Flour due to potential E. coli O26. The product was distributed to commercial bakeries and food service locations.

    Product
    Gold Medal Flour Product Code: 805046 Bulk flour
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1564-2019·2019-07-24

    Recall of Pillsbury Hi Gluten Flour due to E. coli risk

    ADM is recalling Pillsbury Hi Gluten Flour because of potential E. coli O26 contamination. The affected flour was distributed to food service in New York and Pennsylvania.

    Product
    Pillsbury BALANCER HI GLUTEN FLOUR BLEACHED BROMATED ENRICHED 50 LB bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1939-2019·2019-07-24

    Datascope Cardiosave Hybrid Intra-Aortic Balloon Pump Recalled for Labeling Defects

    Datascope Corp. is recalling 6,197 Cardiosave Hybrid Intra-Aortic Balloon Pumps worldwide due to inadequate labeling regarding battery maintenance.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), 0998-00-0800-53 For cardiovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1978-2019·2019-07-24

    CooperSurgical Recalls Advincula Delineator Uterine Manipulator Due to Potential Cracking

    CooperSurgical is recalling 213 units of the Advincula Delineator Uterine Manipulator because the soft cup may crack during use, posing a risk of lacerations.

    Product
    Advincula Delineator with Ultem Plastic Soft Cup size 3.0 cm; Part No. AD750SC-KE30 The Advincula Delineator Uterine Manipulator is a single-use disposable device designed specifically for Total Laparoscopic Hysterectomy (TLH), Laparoscopic Assisted Vaginal Hysterectomy…
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Food)·F-1557-2019·2019-07-24

    Commercial Creamery Recalls White Cheddar Cheese Blend Due to Salmonella Risk

    Commercial Creamery Company of Idaho is recalling White Cheddar 5906-KD because it may be contaminated with Salmonella. The product was distributed in Iowa and Indiana.

    Product
    White Cheddar 5906-KD is a non-GMO White Cheddar Cheese Blend dried cheese powder. Product was shipped in bulk bags, net wt 50 lbs. The product label is read in parts: "***WHITE CHEDDAR BLEND 5906KD *** Net Wt. 50 lbs. ***INGREDIENTS: CHEDDAR CHEESE (Pasteurized Milk, Salt…
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-1578-2019·2019-07-24

    ADM Recalls Bulk Flour Due to Potential E. coli O26 Presence

    ADM is recalling bulk flour products due to the potential presence of E. coli O26. The affected flour was distributed to retailers and commercial bakeries in multiple states.

    Product
    Springup Flr Enr, Mt Bulk Flour Product Code 703020
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·19172·2019-07-24

    Porter-Cable Table Saws Recalled by CPSC Due to Fire Hazard

    Chang Type is recalling Porter-Cable 10-inch table saws sold at Lowe's because the motors can overheat and cause fires. No injuries have been reported.

    Product
    Porter-Cable 10" Table Saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1944-2019·2019-07-24

    Datascope CS300 Intra-Aortic Balloon Pump Recalled for Battery Maintenance Issues

    Datascope Corp. is recalling CS300 Intra-Aortic Balloon Pumps because improper battery maintenance may result in less than the minimum required operating power.

    Product
    CS300 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3023-55 For cardiovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1487-2019·2019-07-24

    Pfizer Recalls Milrinone Lactate Injection Bags Due to Sterility Concerns

    Pfizer is recalling specific lots of Milrinone Lactate Injection bags because they may leak, compromising sterility.

    Product
    Milrinone Lactate Injection 200 mcg (0.2 mg)/mL* in 5% Dextrose Injection, 20 mg/100 mL, 100 mL bag, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-2776-23, Barcode (01)00304092776233.
    Category
    Drug
    Distribution
    2 states
  • SevereNHTSA·19V541000·2019-07-23

    BMW Recalls 2019 X5 and X7 Models for Loose Wheel Bolts

    BMW is recalling 2019 X5 xDrive50i and X7 xDrive40i vehicles because left-side wheel bolts may loosen, increasing the risk of a crash.

    Product
    BMW — BMW X7, X5
    Category
    Vehicle
    Distribution
    Distributed nationwide