State

Nebraska product recalls

73,827 recalls have nationwide distribution and so reach Nebraska. 4,580 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total: 4,580
Critical: 713
Severe: 1,345
Most recent: 2026-10-28

Of the 4,580 recalls naming Nebraska we have scored against our rubric, 713 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,345 (29%) are Severe.

Which agencies issued them

These figures cover only the 4,580 recalls whose distribution notice names Nebraska specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54426–54450 of 78407

SevereFDA (Drugs)·D-0257-2016·2015-11-25
US Compounding Recalls Hyaluronic Acid Syringes Due to Sterility Concerns
US Compounding Inc is recalling 105 syringes of Hyaluronic Acid/Lidocaine due to deficient practices that may impact sterility assurance.
Product
Hyaluronic Acid/Lidocaine (20 mg/1%/2 mL), 3 mL Single Use Syringe, For Intra-Articular Injection, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3239-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0357-2016·2015-11-25
Downing Labs Recalls EDTA Calcium Disodium Injectable Due to Sterility Concerns
Downing Labs is recalling 104 vials of EDTA Calcium Disodium Injectable because the company cannot assure the product's sterility.
Product
EDTA Calcium Disodium Injectable, 300mg/mL, 50mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0375-2016·2015-11-25
Downing Labs Recalls Dexpanthenol Injection Due to Sterility Concerns
Downing Labs, LLC is recalling 235 vials of Dexpanthenol Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide and internationally.
Product
Dexpanthenol Injection, 250mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0382-2016·2015-11-25
Downing Labs Recalls Thiotic Acid Injection Due to Sterility Concerns
Downing Labs, LLC is recalling Thiotic Acid Injection because the company cannot ensure the product is sterile. The recall affects 7 vials distributed in the US and 17 other countries.
Product
Thiotic Acid Injection, 25mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-326-2016·2015-11-25
Essential Wellness Pharma Recalls Sermorelin Injection Due to Sterility Concerns
Essential Wellness Pharma is recalling Sermorelin 1000 mcg/mL / LIDO 0.2% Injection vials because poor sterile production practices resulted in a lack of sterility assurance.
Product
sermorelin 1000 mcg/mL / LIDO 0.2% Injection, 6 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0229-2016·2015-11-25
Kanan Enterprises Recalls Sweet & Salty Mix for Undeclared Milk
Kanan Enterprises is recalling Sweet & Salty Mix products because they contain undeclared milk. The recall covers multiple package sizes sold under Choice, Speedy, and King's brands.
Product
Sweet & Salty Mix 2.75oz Tube Bag, 5oz Pillow Bag, 6.5oz Pillow Bag, 8oz Stand Up Pouch, 16oz Plastic Jar & 25lb Case. INGREDIENTS: Peanuts (Peanuts, Canola and/or Peanut oil, Salt), Chocolate Buttons***Contains Peanut. Sold under the brand names of: Choice, Speedy & King's.
Category
Food
Distribution
21 states
SevereFDA (Drugs)·D-0369-2016·2015-11-25
Downing Labs Recalls DMSO 99% Injection Due to Sterility Concerns
Downing Labs, LLC is recalling DMSO 99% Injection vials because the product lacks assurance of sterility. The recall affects 187 vials distributed in the US and internationally.
Product
DMSO 99% Injection, 50mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-316-2016·2015-11-25
Essential Wellness Recalls Methylcobalamin Syringes Due to Sterility Concerns
Essential Wellness Pharmacy is recalling Methylcobalamin 20 mg/mL prefilled syringes due to poor sterile production practices that compromised sterility assurance.
Product
Methylcobalamin 20 mg/mL PF Injection, 0.05 mL prefilled syringes, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0358-2016·2015-11-25
Downing Labs Recalls TNPRDC Injection Due to Sterility Concerns
Downing Labs, LLC is recalling 171 vials of TNPRDC Injection because the company cannot assure the sterility of the product. The recall covers all lots distributed nationwide and internationally.
Product
TNPRDC Injection, 6 mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-336-2016·2015-11-25
Essential Wellness Pharma Recalls TRIMIX SPECIAL Injection Due to Sterility Concerns
Essential Wellness Pharma is recalling TRIMIX SPECIAL Injection vials because poor sterile production practices created a lack of sterility assurance for the finished drugs.
Product
TRIMIX SPECIAL (30 mg-1 mg-10 mcg/mL) Injection, 5 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-299-2016·2015-11-25
Essential Wellness Pharma Recalls 17-Alpha Hydroxyprogesterone Injections for Sterility Concerns
Essential Wellness Pharma is recalling 17-Alpha Hydroxyprogesterone injections due to poor sterile production practices that compromised sterility assurance.
Product
17-Alpha Hydroxyprogesterone 250 mg/mL in Castor Oil Injection, 5 mL vials, Rx only, Essential Wellness PHARMACY, 4625 N. University, Peoria, IL 61614.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0266-2016·2015-11-25
US Compounding Recalls Methylprednisolone Vials Due to Sterility Concerns
US Compounding Inc is recalling 22,627 vials of Methylprednisolone PF (80 mg/mL) because deficient practices may have impacted sterility assurance.
Product
MethylPREDNISolone PF (80 mg/mL), 1 mL Single Use Vial, For IM & Regional Injection, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3119-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0281-2016·2015-11-25
US Compounding Recalls Testosterone Cypionate Vials Due to Sterility Concerns
US Compounding Inc is recalling 2,524 vials of Testosterone cypionate, USP due to deficient practices that may impact sterility assurance.
Product
Testosterone cypionate, USP (250 mg/mL), 10 mL Multi-Dose Vial, For Deep IM Injection Only, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72653, NDC 62295-2131-07
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0247-2016·2015-11-25
US Compounding Recalls Dapiprazole Ophthalmic Vials Due to Sterility Concerns
US Compounding Inc is recalling 2,984 bottles of compounded Dapiprazole ophthalmic vials nationwide due to deficient practices that may impact sterility assurance.
Product
Dapiprazole (Diluent+Powder) 0.5% in 5 mL vial, For topical ophthalmic use, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-0201-99
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0258-2016·2015-11-25
US Compounding Recalls Hyaluronidase PF Vials Due to Sterility Concerns
US Compounding Inc is recalling 1,096 vials of Hyaluronidase PF (150 units/mL) nationwide due to deficient practices that may impact sterility assurance.
Product
Hyaluronidase PF (150 units/mL) in 1 mL Single-Use Vial, Not for IV Use, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3239-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0280-2016·2015-11-25
US Compounding Recalls Succinylcholine Chloride Syringes Due to Sterility Concerns
US Compounding Inc is recalling 1,590 syringes of Succinylcholine Chloride because deficient practices may have impacted sterility assurance.
Product
Succinylcholine Chloride (200 mg/10 mL), 10 mL Single Use Syringe (20 mg/mL), For IV use, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72653, NDC 62295-3292-07
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0362-2016·2015-11-25
Downing Labs Recalls TNPDR Injection Buffered Due to Sterility Concerns
Downing Labs, LLC is recalling 481 vials of TNPDR Injection Buffered because the company cannot ensure the product is sterile. The recall covers all lots distributed nationwide and internationally.
Product
TNPDR Injection Buffered, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0374-2016·2015-11-25
Downing Labs Recalls DMAE Injection Due to Sterility Concerns
Downing Labs, LLC is recalling DMAE Dimethylaminoethanol Injection due to a lack of assurance of sterility. The recall affects 16 vials distributed nationwide and internationally.
Product
DMAE Dimethylaminoethanol Injection, 100mg/mL, 30mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0347-2016·2015-11-25
Downing Labs Recalls Vitamin D3 Injectable Due to Sterility Concerns
Downing Labs, LLC is recalling Vitamin D3 Injectable, 10,000 U/mL, 10mL vials due to a lack of assurance of sterility. The product was distributed nationwide and internationally.
Product
Vitamin D3 Injectable, 10,000 U/mL, 10mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0377-2016·2015-11-25
Downing Labs Recalls Zinc Sulfate Injection Due to Sterility Concerns
Downing Labs, LLC is recalling 74 vials of Zinc Sulfate Injection due to a lack of assurance of sterility. The product was distributed nationwide and internationally.
Product
Zinc Sulfate (Elemental) Injection, 10mg/mL, 30 mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0264-2016·2015-11-25
US Compounding Recalls Methylcobalamin Vials Due to Sterility Assurance Concerns
US Compounding Inc is recalling 265 vials of Methylcobalamin injection due to deficient practices that may impact sterility assurance.
Product
Methylcobalamin (12.5 mg/mL), 2.5 mL Multi-Dose Vial, For IM or SC Injection, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3251-04.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0250-2016·2015-11-25
US Compounding Recalls Dexamethasone Sodium Phosphate Vials Due to Sterility Concerns
US Compounding Inc is recalling 235 vials of Dexamethasone Sodium Phosphate PF due to deficient practices that may impact sterility assurance.
Product
Dexamethasone Sodium Phosphate PF (10 mg/mL), 2 mL Single Use Vial, For IV or IM Use Only, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3227-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0343-2016·2015-11-25
Downing Labs Recalls MICML TRNDPPC Injection Due to Sterility Concerns
Downing Labs, LLC is recalling MICML TRNDPPC Injection (Preserved) 10mL vials because the company cannot ensure the product is sterile.
Product
MICML TRNDPPC Injection (Preserved) 10mL vial, Rx only, Downing Labs, LLC 4001 McEwen Rd, Suite 110, Dallas TX, 754244, 1-800-914-7435
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0291-2016·2015-11-25
US Compounding Recalls Vancomycin Ophthalmic Preparations Due to Sterility Concerns
US Compounding Inc is recalling 494 syringes of Vancomycin Ophthalmic PF due to deficient practices that may impact sterility assurance.
Product
Vancomycin Ophthalmic PF 0.5 mL (5 mg/0.5 mL (10 mg/mL), 1 mL syringe, For Topical Ophthalmic Use, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-0209-64
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0228-2016·2015-11-25
Kanan Enterprises Recalls Mountain Mix for Undeclared Milk
Kanan Enterprises is recalling Mountain Mix trail mix products because they contain undeclared milk. The products were distributed to 21 states and Canada.
Product
Mountain Mix 2oz bag, 7oz pouch, 10oz pouch, 17oz tin, 28oz pouch & 25lb bag. INGREDIENTS: Raisins, Peanuts (Peanuts, Peanut and/or Canola Oil, Salt), Choco Buttons (Sugar, Partially Hydrogenated Vegetable Oil [Contains One or More of the Following: Palm Kernel***Produced in a…
Category
Food
Distribution
21 states