State

Arkansas product recalls

73,478 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 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22051–22075 of 79021

HighFDA (Devices)·Z-1028-2022·2022-05-11
Evans Wedge Orthopedic Surgical Instrument Recalled for Parts Mixed During Rework
restor3d Inc. is recalling 9 units of Evans Wedge Disposable Trials orthopedic surgical instruments because parts from different lots were mixed during a manufacturing rework and relabeling process.
Product
Evans Wedge Disposable Trials, Large Footprint, 8mm Thickness (Model: 6101-22200818). Orthopedic manual surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1021-2022·2022-05-11
In Vitro Diagnostic Estradiol Test Recalled for Falsely Elevated Results
Siemens Healthcare Diagnostics is recalling Atellica IM Enhanced Estradiol (eE2) 500T diagnostic kits that produce falsely elevated test results in plasma specimens, which could lead clinicians to misinterpret patient results.
Product
Atellica IM Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995562 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0838-2022·2022-05-11
Losartan Potassium tablets recalled for AZIDO impurity above limits
Lupin Pharmaceuticals recalls Losartan Potassium tablets for CGMP deviations with AZIDO impurity above limits. The recall affects 657,336 bottles distributed nationwide; no illnesses reported.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V323000·2022-05-11
Nova Bus Recalls LFS and LFS Artic Buses Due to Signal Confusion
Nova Bus is recalling 2016-2020 LFS and 2013-2022 LFS Artic buses because a text message board duplicates stop and turn signals, increasing crash risk.
Product
NOVA BUS — NOVA BUS LFS ARTIC, LFS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1029-2022·2022-05-11
Robotic-Assisted Medical Device Recalled Due to Software Defect
The FDA is recalling the VELYS Robotic-Assisted Solution Base due to a software defect in version 1.5.1 related to Daylight Saving Time changes. The defect can cause system errors requiring restart, potentially delaying patient treatment.
Product
VELYS Robotic-Assisted Solution Base Product No.: 451570100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1024-2022·2022-05-11
Siemens ADVIA Centaur Estradiol Test Recalled for Falsely Elevated Results
Siemens Healthcare is recalling all lots of the ADVIA Centaur Enhanced Estradiol diagnostic test because plasma specimens can produce falsely elevated results, potentially leading clinicians to misinterpret patient results.
Product
ADVIA Centaur Enhanced Estradiol (eE2) 500T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10491445 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1020-2022·2022-05-11
Estradiol diagnostic test kits recalled for falsely elevated results
Siemens Atellica IM Enhanced Estradiol test kits can produce falsely elevated results in plasma specimens, potentially leading to misinterpretation of patient hormone measurements. Approximately 2,044 units worldwide are affected.
Product
Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10995561 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1025-2022·2022-05-11
Estradiol Diagnostic Device Recalled for Falsely Elevated Test Results
An estradiol diagnostic device has been recalled because it produces falsely elevated test results in plasma specimens. These inaccurate results could cause clinicians to misinterpret patient test results.
Product
ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro diagnostic use in the quantitative detection of estradiol SMN: 10697757 All lots
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0834-2022·2022-05-11
Losartan Potassium Tablets Recalled for Excessive Azido Impurity
Macleods Pharma is recalling Losartan Potassium Tablets due to CGMP deviations with azido impurity levels exceeding acceptable limits. The recall affects 5.6 million tablets distributed nationwide.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0831-2022·2022-05-11
Drug recall: Vancomycin HCl injection bags for manufacturing deviations
SCA Pharmaceuticals has recalled Vancomycin HCl 1.5g injection bags due to manufacturing process deviations. The product was distributed nationwide.
Product
Vancomycin HCl 1.5 g in 0.9% Sodium Chloride, 500 mL bags, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-0924-44
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0851-2022·2022-05-11
Erythromycin Topical Gel Recalled Due to Manufacturing Quality Deviations
McKesson Corporation is recalling Erythromycin Topical Gel USP 2% due to CGMP deviations. The manufacturer discontinued its stability study program, prompting a nationwide recall of all products within their expiration date.
Product
Erythromycin Topical Gel USP, 2%, Net Wt 60 g tube, Rx only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310 Distributed by: McKesson Corporation dba Sky Packaging 4971 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-053-68
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0846-2022·2022-05-11
Lidocaine Oral Topical Solution Recalled Due to Failed Viscosity Specification
Akorn, Inc. is recalling 66,744 bottles of Lidocaine Hydrochloride Oral Topical Solution, USP 2% (Lot #370978) nationwide because the product's viscosity was below the required specification.
Product
Lidocaine Hydrochloride Oral Topical Solution, USP (Viscous) 2%, 100 mL per bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701, NDC 50383-775-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1026-2022·2022-05-11
Cervical Cage Trial Kit Recalled for Incorrect Size Labeling
restor3d Inc. is recalling 14 units of its Non-Sterile Double Ended Trial Kit because the product was labeled as Small Footprint when it is actually Medium. The lot was distributed nationwide across seven states.
Product
Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the Cervical Cage. The kit includes 3 trials. Orthopedic manual surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0829-2022·2022-05-11
Norepinephrine Injection Recalled Nationwide for Manufacturing Quality Deviations
SCA Pharmaceuticals recalled 120 bags of Norepinephrine 8mg injection nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The voluntary recall was initiated April 25, 2022.
Product
Norepinephrine 8mg in 0.9% Sodium Chloride 250 mL bag, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-078-40
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0842-2022·2022-05-11
Losartan Potassium and Hydrochlorothiazide Tablets Recalled for Impurity
Lupin Pharmaceuticals is recalling Losartan Potassium and Hydrochlorothiazide 100 mg/25 mg tablets nationwide due to AZIDO impurity levels above acceptable limits. Patients should consult their healthcare provider about their medication.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0837-2022·2022-05-11
Losartan Potassium and Hydrochlorothiazide Tablets Recalled Due to AZIDO Impurity Contamination
Macleods Pharma USA is recalling Losartan Potassium and Hydrochlorothiazide tablets due to AZIDO impurity levels exceeding acceptable manufacturing standards. The prescription blood pressure medication was distributed nationwide.
Product
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0830-2022·2022-05-11
Drug recall: fentanyl and bupivacaine injectable solution manufacturing deviations
SCA Pharmaceuticals voluntarily recalled 424 bags of fentanyl and bupivacaine injectable solution due to manufacturing control deviations. The product was distributed nationwide in the United States.
Product
Fentanyl 2mcg/ml and Bupivacaine 0.125% in 0.9% Sodium Chloride 100 mL bags, Rx only, SCA Pharmaceuticals Windsor, CT 06095, NDC 70004-0231-32
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V320000·2022-05-10
Land Rover Recalls 2022 New Range Rovers for Front Crash Sensor Defect
Jaguar Land Rover is recalling 2022 New Range Rovers because improperly tightened fasteners may cause front crash sensors to malfunction, affecting air bag deployment.
Product
LAND ROVER — LAND ROVER NEW RANGE ROVER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V318000·2022-05-10
Braxton Creek Recalls 2022 Travel Trailers Due to LP Gas Leak Risk
Braxton Creek RV is recalling 2022 Free Solo, Bushwhacker, and Bushwhacker Plus travel trailers because cracked LP gas fittings may cause a leak and fire.
Product
BRAXTON CREEK — BRAXTON CREEK BUSHWACKER, BUSHWACKER PLUS, FREE SOLO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V319000·2022-05-10
2022 Rivian R1T front passenger seat airbag may not deactivate for children
Certain 2022 Rivian R1T vehicles have a malfunctioning occupant classification system that fails to deactivate the front passenger airbag when a child or child seat is present, increasing injury risk during a crash.
Product
RIVIAN — RIVIAN R1T
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V313000·2022-05-09
2023 Winnebago Ekko RV Recalled for Cracked LP Gas Fittings
Winnebago is recalling 2021-2023 Ekko recreational vehicles because quick disconnect fittings in the LP gas system may crack, potentially causing a gas leak that could lead to fire.
Product
WINNEBAGO — WINNEBAGO EKKO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V316000·2022-05-09
Custom Fire Recalls Spartan Emergency Vehicles Due to Axle Defect
Custom Fire is recalling 2021-2022 Spartan emergency vehicles because a rear axle part may fracture, potentially causing the parking brake to engage unexpectedly and increasing crash risk.
Product
CUSTOM FIRE — CUSTOM FIRE SPARTAN METROSTAR, SPARTAN METROSTAR RT, SPARTAN GLADIATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V315000·2022-05-09
Mercedes-Benz Recalls Vehicles Due to Brake Booster Corrosion Risk
Mercedes-Benz is recalling 2006-2012 ML, GL, and R-Class vehicles because moisture in the brake booster can cause corrosion, leading to reduced brake performance or failure.
Product
MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ R350, ML350, AMG ML63, GL320
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V314000·2022-05-09
Mercedes-Benz Recalls 2021 GLB 250 for Rear Axle Sensor Defect
Mercedes-Benz is recalling 2021 GLB 250 vehicles because a rear axle sensor linkage may be improperly installed, potentially causing headlight glare that increases crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLB 250
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V317000·2022-05-09
2020-2021 Tesla Model 3: Swapped Camera Terminals Impair Collision Detection
Tesla recalls 2020-2021 Model 3 and 2021 Model Y vehicles due to incorrectly installed camera cable terminals that cause swapped camera views, impairing collision detection and automatic emergency braking.
Product
TESLA — TESLA MODEL Y, MODEL 3
Category
Vehicle
Distribution
Distributed nationwide