State

Arkansas product recalls

73,382 recalls have nationwide distribution and so reach Arkansas. 5,542 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total: 5,542
Critical: 1,029
Severe: 1,446
Most recent: 2026-09-23

Of the 5,542 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 5,542 recalls whose distribution notice names Arkansas specifically. The 73,382 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20026–20050 of 78924

HighFDA (Drugs)·D-1490-2022·2022-09-14
Guaifenesin and dextromethorphan liquid medication recalled for manufacturing control issues
Plastikon Healthcare LLC is recalling guaifenesin and dextromethorphan liquid medication (280,500 cups) distributed nationwide due to manufacturing control deviations in production.
Product
GUAIFENESIN AND DEXTROMETHORPHAN 100 mg-10 mg/5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152. NDC 0904-6844-70
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1492-2022·2022-09-14
CORRECTDOSE Children's Allergy Relief Recalled Due to Manufacturing Process Control Deviations
CORRECTDOSE Children's Allergy Relief (Diphenhydramine HCl 12.5 mg per 5 mL) is being recalled nationwide. The FDA determined products were manufactured under conditions with inadequate process control.
Product
CORRECTDOSE Children's ALLERGY RELIEF (Diphenhydramine HCl 12.5 mg per 5 mL), 2.04 FL. OZ (60 mL) packaged in 12- 5mL individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-302-05 UPC 8 60003 67144 3
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1484-2022·2022-09-14
Acetaminophen Oral Solution 160 mg Recalled for Manufacturing Control Deviations
Acetaminophen Oral Solution 160 mg/5 mL (290,270 cups) recalled nationwide due to CGMP manufacturing control deviations. Product was distributed to institutional healthcare facilities.
Product
Acetaminophen Oral Solution 160 mg / 5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6738-70
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1684-2022·2022-09-14
Early Bird Bleed Monitoring System Introducer fails to power on
Saranas, Inc. is recalling 953 units of the Early Bird Bleed Monitoring System Introducer Sheath Set due to a design error that prevents the device from powering on and completing self-tests. The product was distributed nationwide.
Product
Early Bird Bleed Monitoring System Introducer Sheath Set, REF: FG001-01 (6F), FG001-02 (8F)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1488-2022·2022-09-14
Diphenhydramine Solution Recalled Due to Manufacturing Control Deviations
Plastikon Healthcare LLC is recalling Diphenhydramine HCl Oral Solution nationwide due to manufacturing control deficiencies that did not meet Current Good Manufacturing Practice standards.
Product
Diphenhydramine HCl Oral Solution 12.5 mg / 5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6740-70
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1487-2022·2022-09-14
Calcium Carbonate Oral Suspension Recalled Due to Manufacturing Control Deviations
Plastikon Healthcare recalls 49,280 cups of Calcium Carbonate Oral Suspension (1250 mg/5 mL) distributed nationwide due to manufacturing process control failures during production.
Product
CALCIUM CARBONATE ORAL SUSPENSION, 1250 mg/5 mL, 5 mL cup, packaged in 10 cups per tray, 4 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-7098-94
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1661-2022·2022-09-14
Handheld ultraviolet-C germicidal wand recalled for excessive radiation
MERCHSOURCE LLC is recalling a handheld ultraviolet-C germicidal wand (model 1013622) due to excessive ultraviolet-C radiation emission. Consumers should stop using the product immediately.
Product
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1676-2022·2022-09-14
Laboratory diagnostic system may report inaccurate results during shutdown
The VITROS XT 7600 laboratory analyzer may report inaccurate test results when the system performs a shutdown. The issue affects approximately 1,148 units distributed worldwide.
Product
VITROS XT 7600 Integrated System with Version 3.7.2 and below Product Code: 6844461
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1675-2022·2022-09-14
VITROS XT 3400 Chemistry System May Produce Inaccurate Test Results
The VITROS XT 3400 Chemistry System may produce inaccurate test results during shutdown due to electrical current shifts. The FDA has classified this Class II recall, affecting 506 units distributed worldwide.
Product
VITROS XT 3400 Chemistry System with Version 3.7.2 and below Product Code: 6844458
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1683-2022·2022-09-14
Medline Chest Tube Kit Recalled for Non-Sterile Tape Component
Medline Industries is recalling Chest Tube Convenience Kits due to non-sterile tape included in the sterile portion of the kit, creating a contamination and infection risk.
Product
Medline CHEST TUBE REORDER NO: DYNJ36762A
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V685000·2022-09-14
2022 Ford Ranger Loose Fuel Line Connection Increases Fire Risk
Ford is recalling certain 2022 Ranger and Explorer models with 2.3L engines due to potentially loose fuel line connections. An improperly tightened connection may result in a fuel leak, increasing the risk of fire.
Product
FORD — FORD EXPLORER, RANGER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1480-2022·2022-09-14
FDA Recalls Milk of Magnesia USP for Manufacturing Control Deviations
Plastikon Healthcare LLC is recalling 502,600 cups of Milk of Magnesia USP due to manufacturing process control deviations. Consumers should discontinue use and consult their healthcare provider if concerned.
Product
MILK OF MAGNESIA USP, 2400 mg/30 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6846-73.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1483-2022·2022-09-14
Magnesium Hydroxide and Aluminum Hydroxide Oral Suspension Recalled for Manufacturing Control Issues
Plastikon Healthcare LLC is recalling an antacid oral suspension due to manufacturing control deviations. No illnesses have been reported.
Product
Magnesium Hydroxide 2400 mg, Aluminum Hydroxide 2400 mg, Simethicone 240 mg MAX, per 30 mL Oral Suspension, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1481-2022·2022-09-14
Milk of Magnesia Recalled for Manufacturing Process Control Issues
Plastikon Healthcare LLC is recalling Milk of Magnesia USP due to manufacturing process control deviations affecting approximately 92,200 cups distributed nationwide.
Product
MILK OF MAGNESIA USP, 2400 mg/10 mL, Magnesium Hydroxide, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6840-72.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1485-2022·2022-09-14
Acetaminophen Oral Solution Recalled Due to Manufacturing Control Deviations
Plastikon Healthcare LLC is recalling Acetaminophen Oral Solution nationwide because manufacturing quality controls were not adequately maintained. Affected product was distributed to institutional healthcare settings.
Product
Acetaminophen Oral Solution, 325 mg / 10.15 mL, 10.15 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6739-71
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1482-2022·2022-09-14
Antacid Suspension Recalled Due to Manufacturing Process Control Deviations
Plastikon Healthcare LLC is recalling multiple lots of antacid suspension because manufacturing processes were not adequately controlled. The product was distributed nationwide to institutions.
Product
Magnesium Hydroxide 1200 mg, Aluminum Hydroxide 1200 mg, Simethicone 120 mg per 30 mL, 30 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6838-73
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V683000·2022-09-13
BMW Recalls 2022 745E Hybrid Vehicles Due to Battery Fire Risk
BMW is recalling one 2022 745E hybrid vehicle because an improperly sized battery cell electrode may cause a short-circuit and increase the risk of fire.
Product
BMW — BMW 745E
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V679000·2022-09-12
Mercedes-Benz Recalls 2021 GLB 250 Vehicles Due to Electrical Fire Risk
Mercedes-Benz is recalling 2021 GLB 250 vehicles because a damaged Electronic Stability Program unit may cause an electrical short circuit, increasing the risk of fire.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLB 250
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V681000·2022-09-12
Commercial Trucks Recalled for Steering Shaft Component Failure
Daimler Trucks North America is recalling 2022-2023 Western Star 47X and 49X commercial trucks because the steering shaft's u-joint pinch bolt may detach, causing loss of steering control.
Product
WESTERN STAR — WESTERN STAR 49X, 47X
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V678000·2022-09-12
Mercedes-Benz Recalls 2022 C 300 Vehicles for Electrical Short Risk
Mercedes-Benz is recalling 2022 C 300 vehicles because moisture in the trunk may cause an electrical short in the signal acquisition module, increasing the risk of fire or crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ C 300
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V677000·2022-09-12
Farber Recalls One 2021 Freightliner XC Due to Lighting Failure Risk
Farber Specialty Vehicles is recalling one 2021 Freightliner XC because an incorrectly installed resistor can cause vehicle lighting to fail, increasing crash risk.
Product
FARBER SPECIALTY — FARBER SPECIALTY FCCC XC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V680000·2022-09-12
Mercedes-Benz Recalls GLE and GLS Models for Rear Window Trim Defect
Mercedes-Benz is recalling certain 2020-2022 GLE and GLS models because rear door window trim bars may detach, creating a road hazard.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLE 400 E, GLE 350, GLE 450, GLS 450
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V682000·2022-09-12
Spartan Fire Recalls 2022 Gladiator and MetroStar Trucks for Parking Brake Defect
Spartan Fire is recalling 2022 Gladiator and MetroStar fire trucks because the front wheel parking brake may not engage, increasing crash risk.
Product
SPARTAN FIRE — SPARTAN FIRE GLADIATOR, METROSTAR
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-09102022-01·2022-09-10
USDA Issues Public Health Alert for HelloFresh Ground Beef Due to E. Coli Risk
USDA FSIS issued a public health alert for specific HelloFresh ground beef packages linked to an E. coli O157:H7 outbreak. Consumers are urged to discard the product.
Product
FSIS Issues Public Health Alert For Specific Ground Beef In HelloFresh Meal Kits Due to Possible E. Coli O157:H7 Contamination
Category
Food
Distribution
Distributed nationwide
SevereCPSC·22771·2022-09-08
Murphy Beds Recalled Due to Serious Impact and Crush Hazards
Murphy beds sold under Ivy Bronx, Orren Ellis, Stellar Home Furniture, and Wade Logan brand names can break or detach from walls and fall, posing crush and impact hazards. The manufacturer has received 146 reports of failures with 62 injuries.
Product
Ivy Bronx, Orren Ellis, Stellar Home Furniture, and Wade Logan branded Murphy Beds
Category
Consumer Product
Distribution
Distributed nationwide