Nebraska FDA Recalls — Food, Drug, and Medical Device (Past 90 Days)
Source: U.S. Food and Drug Administration (FDA) · openFDA Enforcement API · trailing 90-day window
65
Total active
25
Food
20
Drug
20
Medical Device
What "class" means
The FDA assigns every recall one of three classes based on the severity of harm if a person uses the product:
Class I
Reasonable probability of serious adverse health consequences or death. Stop using immediately and follow return instructions.
Class II
Use may cause temporary or medically reversible adverse effects. Probability of serious harm is remote.
Class III
Not likely to cause adverse health effects — usually quality, labeling, or minor purity issues.
🥗 Food Recalls
Jul 7, 2026
H-1180-2026
Organic Moringa Powder; 15kg/bag (bulk); Product code: GJ96
Recalled by Green Jeeva LLC
Moringa Powder ingredient positive for salmonella
Jul 7, 2026
H-1187-2026
Man Fon Inc. Won Ton Wrappers Extra Thin; Net Wt. 10 oz; UPC# 757168 977315, Keep Refriger
Recalled by Man Fon, Inc.
Undeclared colors: Yellow#5, and Yellow#6.
Jul 7, 2026
H-1188-2026
Wonton Wrappers packed into clear flexible plastic bag and sold as 40 units (16oz bags)/ca
Recalled by Man Fon, Inc.
No labeling. Undeclared wheat and colors: Yellow#5, Yellow#6.
Jul 2, 2026
H-1181-2026
Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 1
Recalled by Frutas y Hortalizas del Sur S.A.
Potential E. coli O145:H28 Contamination
Jul 1, 2026
H-1179-2026
Brooklyn Roasting Company Pasteurized Cold Brew Concentrate; 2.5gal; bag in a box distribu
Recalled by Brooklyn Roasting Works LLC
Ambient storage of the product may lead to Clostridium botulinum toxin formation.
Jun 25, 2026
H-1185-2026
1. TNVitamins 100% Organic Moringa Capsules 1,200 mg 2. TNVitamins 100% Organic Moring
Recalled by Total Nutrition Inc
Contaminated with Salmonella
Jun 24, 2026
H-1149-2026
Fresh to You Burger Chicken Fillet, SKU 10150, Net wt. 5oz. Product is refrigerated. UPC 1
Recalled by Fresh & Ready Foods LLC
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Fillet sandwich. Raw breaded chic
Jun 24, 2026
H-1148-2026
Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is
Recalled by Fresh & Ready Foods LLC
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw b
Jun 24, 2026
H-1186-2026
Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wrapper, 12 p
Recalled by GELLERT GLOBAL GROUP
Undeclared Allergen (Fish)
Jun 23, 2026
H-1143-2026
Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough, 8-oz pouch 12 cookies per po
Recalled by Bear Stewart Co
undeclared soy
Jun 23, 2026
H-1144-2026
Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER; NET WEIGHT: 15 KGS; packaged
Recalled by Trafa Pharmaceutical Inc.
Potential contamination with Salmonella
Jun 23, 2026
H-1150-2026
High Valley Orchard Chocolate Covered Raisins, net wt. 15oz. per package, each case contai
Recalled by Lehi Valley Trading Company, Inc
Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packag
Jun 21, 2026
H-1174-2026
Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place so
Recalled by AMY'S KITCHEN INC.
Potential for spoilage.
Jun 18, 2026
H-1175-2026
OLA-OLA POUNDED GROUNDNUTS (INTWILO) NET WT. 32 oz., 2 lbs. (0.907 kg) Distributed by: Yu
Recalled by Fayus Inc.
Undeclared peanuts
Jun 18, 2026
H-1154-2026
Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48
Recalled by General Mills James Ford Bell Technical Center
Potential foreign material (glass)
Jun 18, 2026
H-1155-2026
Pillsbury Bread Rolls, Kaiser Roll Dough. 144 units / 2.5oz each. Net Wt. 22.5 lb (10.2k
Recalled by General Mills James Ford Bell Technical Center
Potential foreign material (glass)
Jun 17, 2026
H-1129-2026
MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 o
Recalled by MARS SNACKING
Potential contamination with plastic material
Jun 17, 2026
H-1135-2026
Vista MAX; Dietary Supplement, 90 Capsules. Serving Size: 4 Capsules; Distributed by: Visi
Recalled by Provision Health Corp. dba PH Labs
Dietary supplement product Vista MAX contains undeclared Yellow#5.
Jun 17, 2026
H-1134-2026
Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Capsules. Se
Recalled by Provision Health Corp. dba PH Labs
Dietary supplement product Ocular Plus contains undeclared Yellow#5.
Jun 17, 2026
H-1130-2026
MorningStar Farms Hot & Spicy Sausage Patties, 100% Plant Protein Vegan Sausage Patties, N
Recalled by MARS SNACKING
Potential contamination with plastic material
Jun 14, 2026
H-1125-2026
FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. (255g) UPC 797565011830 INGREDIENTS: DA
Recalled by Western Mixers Produce & Nuts, Inc.
Undeclared peanuts.
Jun 12, 2026
H-1177-2026
Vintage Roots Root Beer Syrup, packaged in glass bottle. Net Wt. 8oz. (236.6 mL). Distribu
Recalled by Vintage Roots LLC
Unapproved food additive: sassafras bark.
Jun 12, 2026
H-1137-2026
a.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0
Recalled by NARA ORGANICS INC
Product may be contaminated with Clostridium botulinum.
Jun 10, 2026
H-1147-2026
Alabama Banana Pudding Marshmallow, 4 ounce 16 pieces of individual marshmallows packaged
Recalled by Wondermade LLC
Foreign material: small metal pieces
Jun 9, 2026
H-1136-2026
Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic bag, UPC 60
Recalled by Fry Pie Factory LLC
Undeclared allergen (milk) and process deviation (product not held under refrigeration as required)
💊 Drug Recalls
Jul 15, 2026
D-0727-2026
Naropin (ropivacaine hydrochloride Injection, USP), 0.5%, 100 mg per 20 mL (5 mg per mL),
Recalled by Fresenius Kabi USA, LLC
Presence of Particulate Matter: Hair was found in products
Jul 15, 2026
D-0728-2026
Xylocaine (lidocaine HCl Injection, USP), 1%, 200 mg per 20 mL (10 mg per mL), 25 Multiple
Recalled by Fresenius Kabi USA, LLC
Presence of Particulate Matter: Hair was found in products
Jul 15, 2026
D-0726-2026
Lidocaine HCl Injection, USP, 2%, 100 mg per 5 mL (20 mg per mL), 25 Single Dose Vials, 5
Recalled by Fresenius Kabi USA, LLC
Presence of Particulate Matter: Hair was found in products
Jul 15, 2026
D-0729-2026
Xylocaine (lidocaine HCl Injection, USP), 1%, 500 mg per 50 mL (10 mg per mL), 25 Multiple
Recalled by Fresenius Kabi USA, LLC
Presence of Particulate Matter: Hair was found in products
Jul 15, 2026
D-0725-2026
Glycopyrrolate Injection, USP, 1 mg per 5 mL (0.2 mg per mL), 25 x 5 mL fill in a 6.5 mL
Recalled by Fresenius Kabi USA, LLC
Presence of Particulate Matter: Hair was found in product
Jul 14, 2026
D-0713-2026
Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use
Recalled by Asclemed USA Inc.
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Jul 13, 2026
D-0716-2026
Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 90, 0.2
Recalled by Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Jul 13, 2026
D-0722-2026
Rohto Cooling Eye Drops Cool Relief (naphazoline hydrochloride 0.012%, polysorbate 80 0.2%
Recalled by Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Jul 13, 2026
D-0719-2026
Rohto Cooling Eye Drops Digi Eye (hypromellose 0.35%, tetrahydrozoline HCl 0.05%), Sterile
Recalled by Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Jul 13, 2026
D-0720-2026
Rohto Cooling Eye Drops Dry Aid (povidone 0.68%, propylene glycol 0.3%), Sterile, 0.34 FL
Recalled by Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Jul 13, 2026
D-0717-2026
Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 80 0.2%
Recalled by Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Jul 13, 2026
N/A
Glycopyrrolate Oral Solution, 1 mg/5 mL, delivers 5 mL, Rx only, Pkg: Precision Dose, Inc,
Recalled by Precision Dose Inc.
Due to an out-of-specification result for an unidentified impurity detected during routine stability testing.
Jul 13, 2026
D-0718-2026
Rohto Cooling Eye Drops Optic Glow (naphazoline hydrochloride 0.03%, povidone 0.5%, propyl
Recalled by Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Jul 13, 2026
D-0715-2026
Rohto Cooling Eye Drops ALL-IN-ONE (hypromellose 0.2%, tetrahydrozoline HCL 0.05%, zinc su
Recalled by Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Jul 13, 2026
D-0721-2026
Rohto Cooling Eye Drops Dry Aid (povidone 0.68%, propylene glycol 0.3%), Sterile, TWIN PAC
Recalled by Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Jul 12, 2026
D-0709-2026
Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 10 Tablets (10 x 1) unit dose bliste
Recalled by Major Pharmaceuticals
Subpotent Drug
Jul 12, 2026
D-0711-2026
Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg), 10 Tablets (10 x 1) unit dose blis
Recalled by Major Pharmaceuticals
Subpotent Drug
Jul 12, 2026
D-0703-2026
Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 100 Tablets (10 x 10 unit dose blist
Recalled by Major Pharmaceuticals
Subpotent Drug
Jul 12, 2026
D-0702-2026
Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 100 Tablets (10 x 10 unit dose blist
Recalled by Major Pharmaceuticals
Subpotent Drug
Jul 12, 2026
D-0710-2026
Levothyroxine Sodium Tablets, USP, 125 mcg (0.0125 mg), 10 Tablets (10 x 1) unit dose blis
Recalled by Major Pharmaceuticals
Subpotent Drug
🩺 Medical Device Recalls
Jul 6, 2026
Z-2761-2026
Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual disp
Recalled by Olympus Corporation of the Americas
Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.
Jun 29, 2026
Z-2725-2026
Rapid Refill Continuous Injection System, UPN M00566001
Recalled by Boston Scientific Corporation
Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe lo
Jun 29, 2026
Z-2775-2026
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Recalled by KENT IMAGING, INC.
The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a
Jun 23, 2026
Z-2759-2026
Hotline Fluid Warming Set, single use device, is designed to warm blood and intravenous fl
Recalled by ICU Medical Inc.
ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due t
Jun 18, 2026
Z-2760-2026
Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended
Recalled by Ferno-Washington Inc
Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly
Jun 18, 2026
Z-2771-2026
Boston Scientific TheraSphere 360 Y-90 Management Platform, Model Number M00139509001; Rad
Recalled by Boston Scientific Corporation
Software anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculat
Jun 16, 2026
Z-2768-2026
Ventriculostomy Kit, REF: 46154
Recalled by Medtronic Neurosurgery
Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit en
Jun 16, 2026
Z-2758-2026
P28 PHANTON INTRAMEDULLARY NAIL SYSTEM, Phantom Hindfoot TTC/TC Ball Tipped Guide Rod, SIZ
Recalled by Paragon 28, Inc.
Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging.
Jun 15, 2026
Z-2778-2026
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Recalled by Medtronic MiniMed, Inc.
For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct hig
Jun 15, 2026
Z-2644-2026
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer;
Recalled by Accuray Incorporated
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operat
Jun 15, 2026
Z-2776-2026
Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4
Recalled by Olympus Corporation of the Americas
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation)
Jun 15, 2026
Z-2640-2026
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer;
Recalled by Accuray Incorporated
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operat
Jun 11, 2026
Z-2746-2026
ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of
Recalled by Tosoh Bioscience Inc
The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated I
Jun 10, 2026
Z-2755-2026
FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into th
Recalled by Boston Scientific Corporation
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with
Jun 10, 2026
Z-2753-2026
FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percut
Recalled by Boston Scientific Corporation
Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for us
Jun 10, 2026
Z-2682-2026
ABIOMED Impella CP Set, Pump Set Code 0048-0003, containing BIOMED Impella Introducer, 14
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
Jun 10, 2026
Z-2750-2026
FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401; Percut
Recalled by Boston Scientific Corporation
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter infor
Jun 10, 2026
Z-2685-2026
ABIOMED Impella CP Introducer Kit 14 Fr, 13 cm, Pump Set Code 0052-0038, containing Kit, 1
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
Jun 10, 2026
Z-2683-2026
ABIOMED Impella CP Introducer Kit 14 Fr, 13 and 25 cm, Pump Set Code 1000550, containing K
Recalled by Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr an
Jun 10, 2026
Z-2751-2026
FARASTAR Pulsed Field Ablation Generator, Product ID M004PFCE61M401; Percutaneous Cardiac
Recalled by Boston Scientific Corporation
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter infor
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Subscribe at FDA.gov ↗What you can do
- Check the official FDA recall search at fda.gov/safety/recalls for the most current list.
- If you have a recalled product: stop using it, photograph the package + lot number for your records, and follow the return/refund instructions on the FDA enforcement record.
- For prescription drug recalls: do not stop a medication on your own — call your doctor or pharmacist first. They may swap to a different manufacturer's version of the same drug.
- For Class I food recalls: throw out the product. Don't donate it. Wipe down shelves and surfaces that touched it.
- Also check non-FDA recalls: USDA meat/poultry and CPSC consumer products (toys, appliances, etc.).
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