State

Arkansas product recalls

73,491 recalls have nationwide distribution and so reach Arkansas. 5,543 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total: 5,543
Critical: 1,029
Severe: 1,446
Most recent: 2026-10-14

Of the 5,543 recalls naming Arkansas we have scored against our rubric, 1,029 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,446 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,543 recalls whose distribution notice names Arkansas specifically. The 73,491 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23226–23250 of 79034

ModerateFDA (Drugs)·D-0508-2022·2022-02-09
Nutralox Mint Antacid Chewable Tablets Recalled for cGMP Deviations
Ultra Seal Corporation is recalling 1,486,050 packets of Nutralox Mint Antacid chewable tablets (calcium carbonate 420mg, 2-count packets) distributed nationwide due to current Good Manufacturing Practice (cGMP) deviations.
Product
Nutralox Mint Antacid (calcium carbonate 420mg) Chewable tablets, 2-count packets, Manufactured for: HARTHealth Seattle, WA 98124
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0464-2022·2022-02-09
Nasal & Sinus Decongestant Recalled for cGMP Deviations
Ultra Seal Corporation is voluntarily recalling Nasal & Sinus Decongestant packets containing phenylephrine HCl 5mg due to current good manufacturing practice (cGMP) deviations. The recall affects 3,508,200 packets distributed nationwide.
Product
Nasal & Sinus Decongestant (phenylephrine HCl 5mg) 2 tablets per packet, Mfd. for Cintas First Aid & Safety, Mason OH 45040
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0520-2022·2022-02-09
Tretinoin Capsules 10 mg Recalled for Failed Dissolution Specifications
Teva Pharmaceuticals USA is recalling Tretinoin Capsules 10 mg due to failed dissolution specifications and out-of-specification test results. Approximately 1,175 bottles distributed nationwide may not dissolve properly.
Product
Tretinoin Capsules, 10 mg, 100 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0555-0808-02
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0512-2022·2022-02-09
AYPANAL Pain Reliever Tablets Recalled for Manufacturing Deviations
Ultra Seal Corporation is recalling AYPANAL Non-aspirin Pain Reliever tablets (acetaminophen 325 mg) in 2-count packets nationwide due to Current Good Manufacturing Practice (cGMP) deviations.
Product
AYPANAL Non-aspirin Pain Reliever (acetaminophen 325 mg) tablets, 2-count packets, Dist. by Honeywell Safety Products USA, Smithfield, RI 02917
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0480-2022·2022-02-09
Cold Relief Drug Recalled for Manufacturing Deviations
Ultra Seal Corporation is recalling 227,010 packets of Cold Relief Severe Pain/Cough due to cGMP deviations. The recall affects Lot #AK9436 (expiration 01/2022) distributed nationwide.
Product
Cold Relief Severe Pain/Cough (acetaminophen 325mg, Dextromethorphan HBr 15mg, Guaifenesin 200mg, phenylephrine HCl 5mg), 2-tablet packets, Manufactured for Select Corporation, Carrollton, TX 75007
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0479-2022·2022-02-09
Lite Remfresh Melatonin Tablets Recalled for cGMP Deviations
Ultra Seal Corporation is recalling Lite Remfresh Advanced Ion-Powered Melatonin 0.5mg tablets nationwide due to cGMP (current good manufacturing practices) deviations. The recall affects 25,776 blisters in lots 19E058A and 19E058B with an expiration date of May 2022.
Product
Lite Remfresh Advanced Ion-Powered Melatonin (Melatonin 0.5mg) Tablets, 36-count blisters, Physician's Seal LLC, Boca Raton, FL 33487
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0513-2022·2022-02-09
Sinus Decongestant Nasal Tablets Recalled for cGMP Deviations
Ultra Seal Corporation is recalling 448,300 packets of SINUS DECONGESTANT (phenylephrine HCl 5mg) tablets due to current Good Manufacturing Practice (cGMP) deviations. The recall affects nationwide distribution.
Product
SINUS DECONGESTANT Nasal Decongestant (phenylephrine HCl 5mg) tablets, 2-count packets, Dist. by Honeywell Safety Products USA, Smithfield, RI 02917
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0503-2022·2022-02-09
PEPTIME Energy Caffeine Tablets Recalled for cGMP Deviations
Ultra Seal Corporation is voluntarily recalling PEPTIME Energy (caffeine 350mg) tablets due to cGMP (current good manufacturing practice) deviations. The recall affects 113,040 packets and 7,132 bottles distributed nationwide.
Product
PEPTIME Energy (caffeine 350mg) tablets, packaged in a) 6 count packets and b) 100-count bottles, Marketed by: DMD Pharmaceuticals, A Division of Dickery Consumer Products, Inc., Noblesville, IN 46060.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0516-2022·2022-02-09
REMfresh Advanced Ion-Powered Melatonin Caplets Recalled for cGMP Deviations
Ultra Seal Corporation is voluntarily recalling REMfresh Advanced Ion-Powered Melatonin 2 mg Caplets nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall affects 12-count and 36-count blister packages distributed across the United States.
Product
REMfresh Advanced Ion-Powered Melatonin (Melatonin 2 mg) Caplets, packaged in a) 12-count blisters b) 36-count blisters Physician's Seal LLC, Boca Raton, FL 33487
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0475-2022·2022-02-09
Drug recall: MidNite Sleep Health melatonin tablets, cGMP deviations
Ultra Seal Corporation is voluntarily recalling MidNite Sleep Health melatonin tablets nationwide due to current good manufacturing practice (cGMP) deviations. Approximately 2.2 million bottles are affected.
Product
MidNite Sleep Health (melatonin 1.5 mg) tablets, 30-count bottles, Distributed by: Mylan Consumer Healthcare, Inc. Morgantown, WV 26505 USA
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0492-2022·2022-02-09
Drug Recall: PAINAID Tablets for Manufacturing Deviations
Ultra Seal Corporation is recalling approximately 2.3 million packets of PAINAID pain relief tablets nationwide due to cGMP (current Good Manufacturing Practice) deviations in manufacturing processes.
Product
PAINAID (acetaminophen 110 mg, aspirin 162mg, caffeine 32.4 mg, salicylamide 152mg) 2 tablet packets, Dist. by ZEE Medical Distributors, LLC Mason, OH 45040
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0500-2022·2022-02-09
Magnacal Calcium Carbonate Tablets Recalled for cGMP Deviations
Ultra Seal Corporation is recalling MAGNACAL calcium carbonate 420 mg tablets (Lot #AK9768, expiration 08/2022) nationwide due to current Good Manufacturing Practice (cGMP) deviations. The voluntary recall was initiated on January 24, 2022.
Product
MAGNACAL (calcium carbonate 420 mg), 2 tablet packets, Manufactured for: Afassco Inc. Minden, NV 89423
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0522-2022·2022-02-09
Prescription Drug Recall: Mimvey Mislabeling by Teva Pharmaceuticals
Teva Pharmaceuticals USA is recalling Mimvey (estradiol and norethindrone acetate) tablets nationwide due to mislabeling. The recall affects 6,430 cartons distributed throughout the USA.
Product
MIMVEY — MIMVEY (ESTRADIOL AND NORETHINDRONE ACETATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0521-2022·2022-02-09
Mimvey Estradiol/Norethindrone Prescription Drug Mislabeling Recall
Teva Pharmaceuticals USA is recalling Mimvey (estradiol and norethindrone acetate) tablets nationwide due to mislabeling on certain cartons. The recall affects 218,174 cartons distributed in the United States.
Product
MIMVEY — MIMVEY (ESTRADIOL AND NORETHINDRONE ACETATE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V066000·2022-02-08
Mercedes-Benz Metris Recall for Brake Fluid Reservoir Mounting Defect
Daimler Vans USA is recalling 2016-2021 Mercedes-Benz Metris vehicles because the brake fluid reservoir may detach, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ METRIS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V068000·2022-02-08
Tiffin motorhomes have improperly secured buss bars increasing fire risk
Tiffin is recalling 2018-2022 Allegro and Allegro Breeze motorhomes where an improperly secured electrical buss bar can cause the DC Distribution Panel to overheat and potentially start fires. Dealers will replace the buss bar with a cable for free.
Product
TIFFIN — TIFFIN ALLEGRO, ALLEGRO BREEZE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V067000·2022-02-08
Holiday House Travel Trailers Propane Regulator Failure Risk
Holiday House is recalling certain 2019–2021 travel trailers equipped with defective Winntec propane regulators that may fail and increase propane pressure, raising fire risk in gas appliances.
Product
HOLIDAY HOUSE — HOLIDAY HOUSE 24TB, 27RQ, 18RB
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V065000·2022-02-07
Roadtrek Recreational Vehicles Recalled for Unattached Propane Lines
Roadtrek is recalling certain 2021-2022 recreational vehicles because the propane line may not be attached to the water heater. An unattached propane line can allow gas to enter the vehicle, increasing the risk of a fire.
Product
ROADTREK — ROADTREK ZION SRT, ZION SLUMBER, ZION, PLAY SLUMBER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V064000·2022-02-07
Audi Recalls 2022 Q3 Vehicles for Rearview Camera Software Error
Audi is recalling 2022 Q3 vehicles because a software error may prevent the rearview camera from displaying an image when reversing, increasing crash risk.
Product
AUDI — AUDI Q3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V063000·2022-02-04
Tesla Model Y Boombox Feature May Obscure Pedestrian Warning System
Tesla is recalling certain 2020-2022 Model Y vehicles because the Boombox feature can obscure the Pedestrian Warning System sounds, creating a collision risk. Tesla will disable the Boombox in Drive, Neutral, and Reverse modes via software update.
Product
TESLA — TESLA MODEL 3, MODEL X, MODEL Y, MODEL S
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V062000·2022-02-04
Triumph Recalls 2022 Trident 660 Motorcycles Due to Side Stand Defect
Triumph is recalling 2022 Trident 660 motorcycles because the side stand may bend under weight, causing the bike to become unstable while parked.
Product
TRIUMPH — TRIUMPH TRIDENT 660
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V056000·2022-02-03
Hyundai Recalls Vehicles Due to ABS Module Fire Risk
Hyundai is recalling specific 2014-2019 models because a faulty ABS module could cause an electrical short and engine compartment fire.
Product
HYUNDAI — HYUNDAI TUCSON, SANTA FE, SANTA FE SPORT, SANTA FE XL
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V061000·2022-02-03
Honda Recalls 2021 CBR1000RR-R Fireblade SP Motorcycles for Fire Risk
Honda is recalling 2021 CBR1000RR-R Fireblade SP motorcycles because an overheating exhaust pipe could melt the oil cooler pipe, causing a leak that increases the risk of fire or crash.
Product
HONDA — HONDA CBR1000RR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V060000·2022-02-03
Altec Recalls 2021 Aerial Devices Due to Unintended Boom Movement
Altec is recalling 2021 AH125 aerial devices because a defective component may cause the boom to move unexpectedly, increasing injury risk.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22E006000·2022-02-03
Nexxpro Recalls X.R2 Motorcycle Helmets Due to Impact Protection Defect
Nexxpro is recalling specific X.R2 motorcycle helmets because they may not adequately protect the wearer in a crash. Owners will receive free replacements.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide