State

Arkansas product recalls

72,907 recalls have nationwide distribution and so reach Arkansas. 5,513 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total: 5,513
Critical: 1,018
Severe: 1,210
Most recent: 2026-09-09

Of the 5,513 recalls naming Arkansas we have scored against our rubric, 1,018 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,210 (22%) are Severe.

Which agencies issued them

These figures cover only the 5,513 recalls whose distribution notice names Arkansas specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1476–1500 of 78420

HighFDA (Food)·H-0980-2026·2026-06-10
Albertsons banana nut muffins do not declare walnut allergen
Albertsons store-made Banana Nut Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 434 units are affected.
Product
UPC 22454900000 MUFFINS BANANA NUT 2CT UPC 22120200000 MUFFINS BANANA NUT 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 (Drugs)·D-0574-2026·2026-06-10
GoodSense antacid chewable tablets contain small metallic particles
GoodSense Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of a foreign substance: small metallic particles in the chewable tablets.
Product
GOODSENSE EXTRA STRENGTH ANTACID — GOODSENSE EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0565-2026·2026-06-10
CareOne extra strength calcium antacid tablets contain metallic particles
CareOne Extra Strength Calcium Antacid, calcium carbonate 750 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
EXTRA STRENGTH ANTACID — EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0573-2026·2026-06-10
H-E-B extra strength antacid tablets contain small metallic particles
H.E.B Extra Strength Calcium Carbonate Antacid Tablets, 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
HEB EXTRA STREGTH ANTACID — HEB EXTRA STREGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0993-2026·2026-06-10
Albertsons cocktail tray does not declare almond allergen
An Albertsons store-made cocktail tray is being recalled because the contains statement does not declare almond.
Product
UPC 29133000000 TRAY COCKTAIL 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-0562-2026·2026-06-10
Casey's extra strength antacid tablets contain small metallic particles
Casey's Extra Strength Antacid, calcium carbonate 750 mg chewable tablets, is being recalled because of the presence of small metallic particles in the tablets.
Product
Extra strength Antacid Calcium Carbonate 750 mg, chewable tablets, 96-count bottle, DISTRIBUTED BY CASEY'S MARKETING COMPANY, ANKENY, IA 50521, UPC: 0 98437 24361 9.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2274-2026·2026-06-10
Ivenix infusion pump cassette loading levers may break
The Large Volume Pump of the Ivenix Infusion System is being recalled because of the potential for the Cassette Loading Lever to break. 18,444 installed bases are affected.
Product
The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.
Category
Medical Device
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 (Drugs)·D-0579-2026·2026-06-10
TopCare ultra strength antacid tablets contain small metallic particles
TopCare Health Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
TOPCARE ULTRA STRENGTH ANTACID ASSORTED FRUIT — TOPCARE ULTRA STRENGTH ANTACID ASSORTED FRUIT (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2292-2026·2026-06-10
Arvis Hip and Knee 3.0 trackers may show wear and corrosion
Arvis Hip & Knee 3.0 Instrument Sets are being recalled because the V-Block Assembly and Trackers A, B, C and E may show early wear or corrosion on the exposed magnet face.
Product
Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1016-2026·2026-06-10
Albertsons Waldorf salad does not declare walnut allergen
Albertsons store-made Ready Meals Salad Waldorf is being recalled because the contains statement does not declare walnut. 82 units are affected.
Product
UPC 21163600000 Ready Meals SALAD WALDORF 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 (Food)·H-0991-2026·2026-06-10
Albertsons 16-inch Italian sampler tray does not declare almond
An Albertsons store-made 16-inch Italian sampler tray is being recalled because the contains statement does not declare almond. Nine units are affected.
Product
UPC 29153000000 SAMPLER TRAY ITALIAN 16 INCH 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-2293-2026·2026-06-10
Arvis Hip and Knee 2.0 trackers may show wear and corrosion
Arvis Hip & Knee 2.0 Instrument Sets are being recalled because the Impactor V-Block Assembly and Trackers may show early wear or corrosion on the exposed magnet face.
Product
Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2287-2026·2026-06-10
Philips Azurion 5M20 Roadmap Pro may produce unusable dark images
Philips Azurion 5M20 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 5M20, Model Numbers: 722228 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 (Drugs)·D-0566-2026·2026-06-10
CareOne ultra strength antacid tablets contain small metallic particles
CareOne Ultra Strength Calcium 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 BERRIES — ULTRA STRENGTH ANTACID ASSORTED BERRIES (CALCIUM CARBONATE)
Category
Drug
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 (Drugs)·D-0564-2026·2026-06-10
Market Basket ultra strength antacid tablets contain small metallic particles
Market Basket Antacid, calcium carbonate 1000 mg ultra strength, is being recalled because of the presence of small metallic particles in the chewable tablets.
Product
MARKET BASKET ANTACID Calcium Carbonate 1000 mg, ULTRA STRENGTH, 72 Tablets, Distributed by: De Moules Supermarkets, Inc.,Tewksbury, Mass 01875, UPC 0 49705 83149 6.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0578-2026·2026-06-10
TopCare extra strength antacid tablets contain small metallic particles
TopCare Health Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
TOPCARE EXTRA STRENGTH ANTACID — TOPCARE EXTRA STRENGTH ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0995-2026·2026-06-10
Albertsons imitation crab and shrimp salad does not declare pollock
Albertsons store-made Imitation Crab and Shrimp Salad is being recalled because the contains statement does not declare pollock. 82 units are affected.
Product
UPC 23285300000 IMITATION CRAB AND SHRIMP SALAD 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-0576-2026·2026-06-10
Equaline extra strength antacid tablets contain small metallic particles
Equaline Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Product
EQUALINE EXTRA STRENGTH ASSORTED BERRY ANTACID — EQUALINE EXTRA STRENGTH ASSORTED BERRY ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0555-2026·2026-06-10
Enovachem duloxetine capsules exceed the nitrosamine acceptable intake limit
Duloxetine DR Capsules, 30 mg, relabeled by Enovachem are being recalled over CGMP deviations and N-nitroso-duloxetine above the FDA acceptable intake limit.
Product
DULOXETINE — DULOXETINE (DULOXETINE)
Category
Drug
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 (Devices)·Z-2308-2026·2026-06-10
Stapes prosthesis pistons carry an incorrect functional length on labeling
Titanium/fluoroplastic piston stapes prostheses are being recalled because the device labeling states an incorrect functional length. Seven units are affected.
Product
TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis
Category
Medical Device
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 (Drugs)·D-0557-2026·2026-06-10
Kirkland Signature ultra strength antacid tablets contain metallic particles
Kirkland Signature Ultra Strength Antacid, calcium carbonate 1000 mg, made by Guardian Drug Company for Costco, is being recalled over small metallic particles in the tablets.
Product
KIRKLAND ULTRA STREGTH ANTACID 171AB — KIRKLAND ULTRA STREGTH ANTACID 171AB (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide