State

Minnesota product recalls

72,907 recalls have nationwide distribution and so reach Minnesota. 7,804 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,804
Critical: 1,125
Severe: 1,892
Most recent: 2026-09-09

Of the 7,804 recalls naming Minnesota we have scored against our rubric, 1,125 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,892 (24%) are Severe.

Which agencies issued them

These figures cover only the 7,804 recalls whose distribution notice names Minnesota specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1451–1475 of 80711

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-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 (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-2257-2026·2026-06-10
BD Whitacre 25G spinal trays recalled in Huons bupivacaine sub-recall
BD Spinal Trays with Whitacre needle 25 G, catalog numbers 405637 and 405707, are being recalled as a sub-recall of the Huons bupivacaine product recall. 5,940 units are affected.
Product
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.
Category
Medical Device
Distribution
Distributed nationwide
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-0883-2026·2026-06-10
JCB Flavors fiery hot 25 lb seasoning may contain Salmonella
JCB Flavors Fiery Hot seasoning, item #007415, in 25 lb bags is being recalled because the product may be potentially contaminated with Salmonella. 36 boxes are affected.
Product
#007415 Fiery Hot, Net Wt: 25 lbs. JCB Flavors, 1224 Clark Street, Watertown, WI 53094.
Category
Food
Distribution
4 states
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 (Food)·H-0885-2026·2026-06-10
JCB Flavors butter parsley seasoning may contain Salmonella
JCB Flavors Butter Parsley seasoning in 50 lb boxes is being recalled because the product may be potentially contaminated with Salmonella. Three boxes are affected.
Product
#800414/003729Butter Parsley, Net Wt: 50 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-2248-2026·2026-06-10
BD Quincke spinal trays recalled over Huons bupivacaine quality issues
BD Spinal Trays with a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 990 units are affected.
Product
BD¿Spinal Tray with BD¿Quincke 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: 405609.
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
HighFDA (Food)·H-1033-2026·2026-06-10
Albertsons nine-inch peach melba pies do not declare almond
Albertsons store-made Pie Peach Melba 9-inch is being recalled because the contains statement does not declare almond. Seven units are affected.
Product
UPC 25688000000 PIE PEACH MELBA 9IN 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-0985-2026·2026-06-10
Albertsons pistachio muffins do not declare walnut allergen
Albertsons store-made Pistachio Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 354 units are affected.
Product
UPC 22321200000 MUFFINS PISTACHIO 2CT UPC 22770600000 MUFFINS PISTACHIO 4CT 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-2297-2026·2026-06-10
BD Pyxis MedStation 4000 fingerprint scanner may overheat and burn
The BD Pyxis MedStation 4000 medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Product
BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1013-2026·2026-06-10
Albertsons seafood salad contains statement does not declare crab
Albertsons store-made seafood salad is being recalled because the contains statement does not declare crab. 114 units are affected.
Product
UPC 23625000000 FISH HOUSE PREMIUM SEAFOOD SALAD UPC 21431200000 Ready Meals SALAD SEAFOOD SS UPC 21878600000 SALAD SEAFOOD 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 (Food)·H-1047-2026·2026-06-10
Albertsons ahi poke products do not declare tuna allergen
Albertsons store-made ahi poke products, sold under three UPCs, are being recalled because the contains statement does not declare tuna. 23 units in total are affected.
Product
UPC 23952700000 POKE AHI LIMU UPC 23506700000 POKE AHI LIMU PREVIOUSLY FROZEN - CO UPC 23958200000 POKE AHI SALT & PEPPER This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scal
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2295-2026·2026-06-10
Phothera 200 phototherapy calibration certificates had outputs reversed
Phothera 200 phototherapy devices are being recalled because some Calibration and Output Certificates had the outputs reversed. 368 units are affected.
Product
Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0960-2026·2026-06-10
Albertsons white strawberry cake bars do not declare almond
Albertsons store-made Artisan White Strawberry Cake Bar is being recalled because the contains statement does not declare almond. 173 units are affected.
Product
UPC 22253500000 Cake Bar Artisan White Strawberry Small. 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-0568-2026·2026-06-10
Family Wellness antacid tablets contain small metallic particles
Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
FAMILY WELLNESS ULTRA STRENGTH ASSORTED FRUIT ANTACID — FAMILY WELLNESS ULTRA STRENGTH ASSORTED FRUIT ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-1029-2026·2026-06-10
Albertsons sliced loaf platter does not declare walnut allergen
Albertsons store-made Platter Loaf Sliced, 20 count, is being recalled because the contains statement does not declare walnut. 20 units are affected.
Product
UPC 22650200000 PLATTER LOAF SLC 20CT 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-0974-2026·2026-06-10
Albertsons Dubai chocolate croissants do not declare pistachio
Albertsons store-made Dubai Chocolate Croissants, 2 count, are being recalled because the contains statement does not declare pistachio. 92 units are affected.
Product
UPC 25678000000 CROISSANTS DUBAI CHOCOLATE 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-1019-2026·2026-06-10
Albertsons chicken caesar salad does not declare anchovy allergen
Albertsons store-made chicken caesar salad is being recalled because the contains statement does not declare anchovy. 328 units are affected.
Product
UPC 24512800000 SALAD CHICKEN CAESAR UPC 29854600000 Kitchen SALAD CHICKEN CAESAR 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-2309-2026·2026-06-10
Sharpoint microsurgical knives labeled 2.2mm actually measure 3.0mm
Sharpoint 2.2 mm angled double-bevel microsurgical knives are being recalled because 3.0 mm knives were labeled and packaged as 2.2 mm. 1,818 units affected.
Product
Sharpoint 2.2MM, ANGLED, DOUBLE- BEVEL Model/Catalog Number: 72-2231 Microsurgical Knife
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2289-2026·2026-06-10
Philips Azurion 7B20/15 systems may show unusable dark fluoroscopy images
Philips Azurion 7B20/15 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable. 156 units affected.
Product
Philips Azurion 7B20/15, Model Numbers: 722068, 722226 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 (Devices)·Z-2284-2026·2026-06-10
Philips Azurion 3M12 Roadmap Pro may produce unusable dark images
Philips Azurion 3M12 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 3M12, Model Numbers: 722063, 722221 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-0905-2026·2026-06-10
Second Nature Keto Crunch mix may contain undeclared cashews and pistachios
Second Nature Keto Crunch Smart Mix is being recalled because the product may contain undeclared allergens, specifically cashews and pistachios, along with dried cherries.
Product
SECOND NATURE KETO CRUNCH SMART MIX, 10-ounce retail-sized plastic pouch, UPC 077034013405, 6-10oz units per case.
Category
Food
Distribution
Distributed nationwide