State

Nebraska product recalls

72,907 recalls have nationwide distribution and so reach Nebraska. 4,547 additional recalls listed Nebraska specifically in their distribution scope.

What the numbers show

Total: 4,547
Critical: 705
Severe: 1,119
Most recent: 2026-09-09

Of the 4,547 recalls naming Nebraska we have scored against our rubric, 705 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,119 (25%) are Severe.

Which agencies issued them

These figures cover only the 4,547 recalls whose distribution notice names Nebraska specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1401–1425 of 77454

SevereFDA (Devices)·Z-2254-2026·2026-06-10
BD Whitacre 25 gauge spinal trays recalled over bupivacaine quality issues
BD Spinal Trays with a Whitacre 25 G needle, catalog number 405658, are being recalled as a sub-recall of the Huons bupivacaine product recall. 150 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2252-2026·2026-06-10
BD Whitacre 24 gauge spinal trays recalled over bupivacaine quality issues
BD Spinal Trays with a Whitacre 24 G needle, catalog numbers 400868 and 405652, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,550 units affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2224-2026·2026-06-10
Ivenix infusion pumps may hide internal damage after being dropped
Ivenix Infusion System Large Volume Pumps are being recalled because dropping or jarring can loosen the touchscreen input cable, causing random touches or an unresponsive screen.
Product
Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
Category
Medical Device
Distribution
21 states
SevereFDA (Devices)·Z-2276-2026·2026-06-10
B. Braun spinal needle kits recalled over Huons bupivacaine quality issues
Spinal needle procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection are being recalled after the drug's manufacturer issued a voluntary recall. 582,030 units are affected.
Product
Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862); GOVP24BK 24G PENCAN TRAY W/ BUP & DEXTROS (332607); P24BK 24G PENCAN TRAY W/BUP & DEXTROSE (333868); P
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2251-2026·2026-06-10
BD Whitacre 22G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Whitacre needle 22 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 330 units are affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0909-2026·2026-06-10
Alfredo sauce contains dry milk powder recalled over Salmonella
Alfredo Sauce in 3 lb 7 oz sealed poly bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0039954921963
Category
Food
Distribution
41 states
SevereFDA (Devices)·Z-2278-2026·2026-06-10
Design Options spinal trays recalled over Huons bupivacaine quality issues
Design Options spinal needle anesthesia procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall.
Product
Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C 20061890 (560074), SSK S C H (560214), SSK BJC H S (ORIGINAL CUST) (560272), SSK CA P M C (ORIGINAL CUST) (560327), SSK T M H (560394), SSK S O 20070208 (
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0907-2026·2026-06-10
Cheese sauce mixes contain dry milk powder recalled over Salmonella
Cheese Sauce Mix and Creamier Cheese Sauce Mix are being recalled because they contain a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
1) Cheese Sauce Mix, 25.5 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0399549125016 2) Cheese Sauce Mix, 25 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954924308 3) Creamier Cheese Sauce Mix, 25 lb., packaged in a tied poly bag an
Category
Food
Distribution
41 states
SevereFDA (Devices)·Z-2277-2026·2026-06-10
Spinocan spinal needle kits recalled over Huons bupivacaine quality issues
Spinocan spinal needle procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall. 16,080 units affected.
Product
Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201); Spinocan 25 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333211); Spin
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0908-2026·2026-06-10
Aramark cheese sauce contains dry milk powder recalled over Salmonella
Aramark Cheese Sauce New & Improved in 25 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.
Product
Aramark Cheese Sauce New & Improved, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954925121
Category
Food
Distribution
41 states
HighFDA (Food)·H-0987-2026·2026-06-10
Andronico's sweet start catering tray does not declare walnut
The Andronico's Sweet Start Catering Tray Large, an Albertsons store-made item, is being recalled because the contains statement does not declare walnut. 14 units are affected.
Product
UPC 25047100000 ANDRONICO'S SWEET START CATERING TRAY LARGE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0556-2026·2026-06-10
Ascend amlodipine and olmesartan tablets failed dissolution specifications
Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, are being recalled after failing dissolution specifications, with olmesartan medoxomil content below specification.
Product
AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0560-2026·2026-06-10
Good Neighbor Pharmacy antacid tablets contain small metallic particles
Good Neighbor Pharmacy Extra Strength Antacid, calcium carbonate 750 mg chewable tablets, is being recalled because of the presence of small metallic particles.
Product
GOOD NEIGHBOR PHARMACY ANTACID — GOOD NEIGHBOR PHARMACY ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0981-2026·2026-06-10
Cream cheese filled banana nut muffins do not declare walnut
Albertsons store-made Muffins Banana Nut Cream Cheese Filled 2 count are being recalled because the contains statement does not declare walnut. Nine units are affected.
Product
UPC 25312600000 MUFFINS BANANA NUT CREAM CHEESE FILLED 2CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0978-2026·2026-06-10
Albertsons sub sandwich tray does not declare pistachio allergen
Albertsons store-made Kitchen Tray Sub Sandwich is being recalled because the contains statement does not declare pistachio. 13 units are affected.
Product
UPC 29259700000 KITCHEN TRAY SUB SANDWICH SS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-1020-2026·2026-06-10
Albertsons chicken strip salad does not declare almond allergen
Albertsons store-made Kitchen Salad Chicken Strip is being recalled because the contains statement does not declare almond. 55 units are affected.
Product
UPC 29433900000 Kitchen SALAD CHICKEN STRIP This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2288-2026·2026-06-10
Philips Azurion 7B12 Roadmap Pro may produce unusable dark images
Philips Azurion 7B12/12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Product
Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0971-2026·2026-06-10
Albertsons oatmeal raisin cookies do not declare almond allergen
Albertsons store-made Oatmeal Raisin Cookies, 10 count, are being recalled because the contains statement does not declare almond. 62 units are affected.
Product
UPC 26911700000 COOKIES OATMEAL RAISIN 10CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2301-2026·2026-06-10
BD Pyxis Mini Main cabinets may overheat at fingerprint scanner
BD Pyxis Mini Main medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 709 units affected.
Product
BD Pyxis Mini Main REF: 349 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1072-2026·2026-06-10
Albertsons sweet chili salmon salad omits salmon and walnut declarations
Albertsons store-made Fresh Berry & Sweet Chili Salmon Salad is being recalled because the contains statement does not declare salmon and walnut. Four units are affected.
Product
UPC 21478000000 Ready Meals SALAD FRESH BERRY & SWEET CHILI Salmon SS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2275-2026·2026-06-10
PhaseOne antimicrobial solution sprayer springs may corrode into the product
PhaseOne Antimicrobial Solution is being recalled because the stainless steel spring inside the sprayer can corrode, releasing trace metallic elements into the solution.
Product
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1046-2026·2026-06-10
Albertsons premium broccoli salad does not declare cashew allergen
Albertsons store-made Ready Meals Salad Premium Broccoli is being recalled because the contains statement does not declare cashew. 90 units are affected.
Product
UPC 21600500000 READY MEALS SALAD PREMIUM BROCCOLI SS This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0561-2026·2026-06-10
Good Neighbor Pharmacy 1000 mg antacid tablets contain metallic particles
Good Neighbor Pharmacy Extra Strength Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
ULTRA STRENGTH ANTACID ASSORTED FRUIT — ULTRA STRENGTH ANTACID ASSORTED FRUIT (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2296-2026·2026-06-10
Avanta administration tube sets may not engage the flow control valve
Avanta Multi-Patient Administration Tube Sets are being recalled because supplier changes created a fit issue, so the stopcock cannot be reliably engaged with the Contrast Flow Control Valve.
Product
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1017-2026·2026-06-10
Albertsons apple waldorf salad does not declare walnut allergen
Albertsons store-made Apple Waldorf Salad is being recalled because the contains statement does not declare walnut. 33 units are affected.
Product
UPC 21633500000 READY MEALS SALAD APPLE WALDORF SS UPC 29824500000 Kitchen SALAD APPLE WALDORF FS UPC 27169500000 Kitchen SALAD APPLE WALDORF LRG UPC 27170300000 Kitchen SALAD APPLE WALDORF MED UPC 27169300000 Kitchen SALAD APPLE W
Category
Food
Distribution
Distributed nationwide