The Recall Desk

State

Minnesota product recalls

73,824 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,851
Critical
1,137
Severe
2,246
Most recent
2026-11-04

Of the 7,851 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,246 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51476–51500 of 81675

  • CriticalFDA (Food)·F-0087-2017·2016-10-19

    NatureBox Dark Cocoa Nom Noms Recalled for Undeclared Peanut Allergen

    NatureBox is recalling Dark Cocoa Nom Noms because some bags may contain peanut butter but do not list peanuts on the label.

    Product
    Dark Cocoa Nom Noms 4.5oz. (128g) UPC: 8 54557 00533 5 Lot 16083 Product is shipped directly to customers per individual order or to corporate customers in 20 x 4.5 oz. bags cases. Ingredients: Rolled Oats, Almonds. For address freshness (Grape juice, rice dextrin)…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0094-2017·2016-10-19

    B. Braun Recalls 5% Dextrose Injection Due to Fungal Contamination

    B. Braun Medical Inc. is recalling 57,408 units of 5% Dextrose Injection USP due to non-sterility caused by fungal contamination from leaking containers.

    Product
    5% Dextrose Injection USP, 100mL in a 150 mL PAB container, Rx only, B. Braun Medical Inc. Irvine, CA 92614-5895 USA, NDC 00264-1510-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0047-2017·2016-10-19

    Quaker Quinoa Granola Bars Recalled Due to Listeria Risk

    The Quaker Oats Company is recalling Quaker Quinoa Granola Bars because sunflower kernels used in their production were linked to a Listeria monocytogenes recall.

    Product
    Quaker Quinoa Granola Bars, chocolate nut medley packaged in a multi colored box with brown lettering. Wrapper UPC: 000 30000 00243 8
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0022-2017·2016-10-19

    Diocto Liquid Stool Softener Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Diocto Liquid stool softener bottles due to positive findings of Burkholderia cepacia contamination.

    Product
    Diocto Liquid (docusate sodium) 50 mg/5 mL Stool Softener Laxative, One Pint (473 mL) bottles, Dist by: Rugby Laboratories, Livonia, MI --- NDC 0536-0590-85
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0048-2017·2016-10-19

    Quaker Quinoa Granola Bars Recalled Due to Listeria Risk

    The Quaker Oats Company is recalling Quaker quinoa granola bars because they were made with sunflower kernels contaminated with Listeria monocytogenes.

    Product
    Quaker quinoa granola bars, yogurt fruit and nut flavor packaged in a multi colored box with brown lettering. Wrapper UPC: 000 30000 00195 0
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0049-2017·2016-10-19

    Pharmedium Recalls Heparin Sodium Syringes Due to Subpotency and Stability Concerns

    Pharmedium Services, LLC is recalling 350 syringes of Heparin Sodium Injection USP because confirmed subpotency and stability data do not support the expiry date.

    Product
    HEPARIN Sodium Inj. USP, 3,000 USP Heparin Units per 3 mL Total Volume in a syringe, NOT FOR LOCK FLUSH, 1,000 Heparin USP Units per mL, Rx only, PharMEDium, Product code 2K1926.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0016-2017·2016-10-19

    Leiter's Compounding Recalls Moxifloxacin Intravitreal Injection Due to Sterility Concerns

    Leiter's Compounding is recalling Moxifloxacin intravitreal injections because they were produced using recalled filters, raising concerns about sterility.

    Product
    Moxifloxacin 1 mg/mL in Sterile Balanced Salt Solution (BSS) Intravitreal Injection, 1 mL Total Volume in a 2 mL Vial, Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-003-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0007-2017·2016-10-19

    Cabela's Maple Nut Candies Recalled for Undeclared Peanut Allergen

    Rucker's Wholesale & Service Co. is recalling Cabela's Maple Nut candies because the label fails to list peanuts, a major allergen.

    Product
    Cabela's classic candies Maple nut packaged in 2.7 oz. clear plast ice bag with brown label attached with brown lettering.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0049-2017·2016-10-19

    Nature's Power Solutions Acidophilus Blend Recalled for Undeclared Milk

    Complete Packaging & Manufacturing is recalling Nature's Power Solutions Acidophilus Blend dietary supplements because they contain undeclared milk, a major food allergen.

    Product
    Dietary Supplement Acidophilus Blend, 90 capsules, Product No. E-420, packaged in 225cc HDPE white bottle, room temp, sold individually
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0055-2017·2016-10-19

    Publix Maple Walnut Strip Danish Recalled for Metal Shavings

    Gold Standard Baking is recalling Publix Maple Walnut Strip Danishes due to the presence of small metal shavings.

    Product
    Publix Maple Walnut Strip Danish | Count, 1 | NET WT 14.00 oz | Distributed by Publix Supermarkets, Inc., Lakeland, FL 33802
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0034-2017·2016-10-19

    Pharmedium Recalls Fentanyl Citrate Injection Due to Subpotency and Stability Issues

    Pharmedium Services, LLC is recalling specific lots of fentanyl citrate injection because confirmed subpotency and stability data do not support the expiry date.

    Product
    fentaNYL Citrate Injection, 50 mcg per mL, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3153.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0096-2017·2016-10-19

    Hospira Recalls Marcaine Injection Due to Sterility and Potency Issues

    Hospira is recalling 15 vials of Marcaine 0.25% injection because a glass defect allowed water to enter, compromising sterility and reducing drug potency.

    Product
    MARCAINE — MARCAINE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0011-2017·2016-10-19

    Leiter's Compounding Recalls Brilliant Blue G Injection Due to Sterility Concerns

    Leiter's Compounding is recalling Brilliant Blue G injections because they were produced using recalled filters, raising concerns about sterility.

    Product
    Brilliant Blue G 0.025% in 0.9% Sodium Chloride (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-008-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0067-2017·2016-10-19

    Publix Cherry Strip Danish Recalled for Metal Shavings

    Gold Standard Baking is recalling Publix Cherry Strip Danishes due to the presence of small metal shavings.

    Product
    Publix Cherry Strip Danish | Count, 1 | NET WT 15.00 oz | Distributed by Publix Supermarkets, Inc., Lakeland, FL 33802. UPC: 002-19562-00000
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0006-2017·2016-10-19

    HeartWare HVAD Pump Recalled for Foreign Material in Driveline Connector

    HeartWare is recalling 344 HVAD pumps worldwide because foreign material in the driveline connector could cause electrical faults.

    Product
    HeartWare Ventricular Assist System (HVAD), US product: Model No.: 1103; and International Product: Model No.: 1104XX. Product Usage: For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart…
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Drugs)·D-0057-2017·2016-10-19

    Pharmedium Recalls Ketamine HCl Injection Due to Potential Loss of Potency

    Pharmedium Services, LLC is recalling 54 syringes of ketamine HCl injection because stability data does not support the expiration dates, posing a risk of reduced drug potency.

    Product
    ketamine HCl Injection, 50 mg per mL (100 mg per 2 mL), 2 mL Total Volume in a syringe, Rx only, PharMEDium, For IV Use, Product code 2R3500.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0014-2017·2016-10-19

    FDA Recalls Lidocaine and Phenylephrine Injection Due to Sterility Concerns

    Leiter's Compounding is recalling Lidocaine HCl and Phenylephrine HCl injection vials because they were produced using recalled filters, raising concerns about sterility.

    Product
    Lidocaine HCl 1% - Phenylephrine HCl 1.5% in Sterile Water for Injection (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-002-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0081-2017·2016-10-19

    Pharmedium Recalls Morphine Sulfate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 25 syringes of morphine sulfate 2 mg/mL due to stability data that does not support the expiry date, posing a risk of potential loss of potency.

    Product
    morphine Sulfate, 2 mg per mL, in 0.9% Sodium Chloride, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2T6455.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0068-2017·2016-10-19

    Publix Guava Strip Danish Recalled for Metal Shavings

    Gold Standard Baking is recalling Publix Guava Strip Danishes due to the presence of small metal shavings.

    Product
    Publix Guava Strip Danish | Count, 1 | NET WT 15.00 oz | Distributed by Publix Supermarkets, Inc., Lakeland, FL 33802. UPC: 002-19562-00000
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0064-2017·2016-10-19

    Gold Standard Baking Recalls Strawberry Cheese Danish Due to Metal Shavings

    Gold Standard Baking is recalling The Bakery Strawberry Cheese Danish because of the presence of small metal shavings. The product was distributed nationwide by Walmart.

    Product
    The Bakery Strawberry Cheese Danish | Net Wt 14 OZ (397g) | Distributed By WAL-MART Stores, Inc, Bentonville, AR 72716 | UPC: 078742100401
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0052-2017·2016-10-19

    Pharmedium Recalls Hydromorphone Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 450 syringes of Hydromorphone HCl because stability data does not support the expiry dates, posing a risk of loss of potency.

    Product
    HYDROmorphone HCl, 1 mg per mL, in 0.9% Sodium Chloride, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2T6165
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0018-2017·2016-10-19

    Leiter's Compounding Recalls Vancomycin Injection Due to Sterility Concerns

    Leiter's Compounding is recalling Vancomycin 10 mg/mL injection vials because they were produced using recalled filters, raising concerns about sterility.

    Product
    Vancomycin 10 mg/mL in 0.9% Sodium Chloride (Injection) 1 mL Total Volume in a 2 mL Vial (Preservative Free), Compounded by Leiter's Compounding, San Jose, CA --- NDC 70360-005-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0077-2017·2016-10-19

    Pharmedium Recalls Morphine Sulfate Syringes Due to Stability Data Concerns

    Pharmedium Services, LLC is recalling 935 syringes of morphine sulfate because stability data does not support the expiry dates, posing a risk of reduced potency.

    Product
    morphine Sulfate, 0.5 mg per mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3119.
    Category
    Drug
    Distribution
    Distributed nationwide