State

Arkansas product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24826–24850 of 79052

ModerateFDA (Devices)·Z-2495-2021·2021-09-29
Ad-Tech TECH ATTACH Cable Recalled for Incorrect Label Information
Ad-Tech Medical recalled its Lightweight TECH ATTACH Cable due to incorrect labels on affected units. The cables are designed to connect electrodes to third-party monitors and stimulators.
Product
Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0813-2021·2021-09-29
Sirolimus Tablets Recalled for Failed Impurities and Degradation Specifications
American Health Packaging is recalling Sirolimus 1 mg tablets (Lot #1000789, expiring 10/31/2022) distributed nationwide because they failed impurities and degradation specifications.
Product
SIROLIMUS — SIROLIMUS (SIROLIMUS)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0823-2021·2021-09-29
Drug Recall: Chlorzoxazone Tablets Due to Manufacturing Deviations
Glenmark Pharmaceuticals is recalling 1,800 bottles of Chlorzoxazone Tablets USP 375 mg nationwide due to current Good Manufacturing Practice (CGMP) deviations. The recall was initiated on August 27, 2021.
Product
Chlorzoxazone Tablets USP 375 mg 100 Tablets Rx Only NDC 68462-724-01 Manufactured by: Glenmark Pharmaceuticals Inc., USA 4147 Goldmine Road Monroe, NC 28110 Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0828-2021·2021-09-29
Betadine Povidone-Iodine Solution Swabstick recalled for subpotent drug
Avrio Health L.P. is recalling Betadine Solution Swabstick in single and three-count packages nationwide because the product is subpotent—meaning it contains less active ingredient than specified. Consumers should stop using affected lots and consult their healthcare provider if needed.
Product
BETADINE — BETADINE (POVIDONE-IODINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0808-2021·2021-09-29
Chantix Varenicline Tablets Recalled for Nitroso Impurity
Pfizer is recalling Chantix (varenicline) tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit, a manufacturing deviation.
Product
Chantix (varenicline) tablets 0.5mg/1mg, 56 Tablets, Rx only, Distributed by Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, Made in Ireland, NDC 00069-0471-03. carton containing one blister pack of 11 0.5 mg tablets and one blister pack containing 42.1 mg tablets.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2496-2021·2021-09-29
Ad-Tech TECH ATTACH Cable Recalled Due to Incorrect Labeling
Ad-Tech Medical Instrument Corporation is recalling TECH ATTACH Cables due to incorrect labeling. The cables connect electrodes to third-party monitors and stimulators.
Product
Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0824-2021·2021-09-29
Chlorzoxazone 750 mg Tablets Recalled Due to CGMP Deviations
Glenmark Pharmaceuticals is recalling Chlorzoxazone 750 mg tablets nationwide due to current good manufacturing practice (CGMP) deviations. The voluntary recall affects 4,752 bottles with five affected lot numbers.
Product
Chlorzoxazone Tablets USP 750 mg 100 Tablets Rx Only NDC 68462-725-01 Manufactured by: Glenmark Pharmaceuticals Inc., USA 4147 Goldmine Road Monroe, NC 28110 Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0814-2021·2021-09-29
Promethazine Syrup Plain Recall Due to Microbial Contamination
Morton Grove Pharmaceuticals is recalling Promethazine Syrup Plain 6.25 mg/5 mL in 1-pint bottles due to potential microbial contamination in liquid sugar batches used during manufacturing.
Product
Promethazine Syrup Plain, 6.25 mg/5 mL (Promethazine Hydrochloride Syrup, USP), 1 Pint (473 mL), Rx Only, Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054; Manuractured By: Morton Grove Pharmaceuticals, Inc, Morton Grove, IL 60053. NDC: 60432-608-16
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0810-2021·2021-09-29
Chantix Varenicline Tablets Recalled for N-Nitroso Impurity
Pfizer is recalling specific lots of Chantix (varenicline) 1 mg tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit. The affected lots were distributed nationwide.
Product
CHANTIX — CHANTIX (VARENICLINE TARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0816-2021·2021-09-29
Valproic Acid Oral Solution recalled for microbial contamination
Morton Grove Pharmaceuticals is recalling Valproic Acid Oral Solution (250 mg/5 mL) due to potential microbial contamination in liquid sugar batches used during manufacturing.
Product
Valproic Acid Oral Solution USP, (250 mg/5 mL), 1 Pint (473 mL), Rx Only, Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054; Manuractured By: Morton Grove Pharmaceuticals, Inc, Morton Grove, IL 60053. NDC: 60432-621-16
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0825-2021·2021-09-29
Zonisamide Capsules Recalled for Manufacturing Deviations
Glenmark Pharmaceuticals is recalling Zonisamide Capsules 50 mg nationwide due to manufacturing deviations. The recall affects approximately 15,936 bottles across multiple lots with expiration dates in May 2022.
Product
ZONISAMIDE — ZONISAMIDE (ZONISAMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2486-2021·2021-09-29
Microbiologics SARS-CoV-2 Process Control Pellets Recalled for Product Specification Issue
Microbiologics Inc is recalling 218 units of SARS-CoV-2 process control pellets (catalog HE0062S) used to validate diagnostic tests. The FDA Class II recall involves product composition regarding RNA transcript content.
Product
SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use as an external, non-viable control material to evaluate the performance of nucleic acid tests that detect SARS-CoV-2 virus.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0821-2021·2021-09-29
Glenmark Naproxen Sodium Tablets recalled for CGMP deviations
Glenmark Pharmaceuticals is recalling 9,552 bottles of Naproxen Sodium Tablets USP 275 mg nationwide due to CGMP (current Good Manufacturing Practice) deviations identified at the manufacturing facility.
Product
NAPROXEN SODIUM — NAPROXEN SODIUM (NAPROXEN SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0811-2021·2021-09-29
Chantix (Varenicline) Tablets Recalled for Impurity Above FDA Limits
Pfizer is recalling Chantix (varenicline) 1 mg tablets distributed nationwide due to the presence of N-nitroso-varenicline impurity above the FDA's acceptable interim intake limit. Affected lots have expiration dates from September 2021 to December 2023.
Product
Chantix (varenicline) tablets 1 mg, Carton containing 4 blister packs of 14 tablets each,, Rx only, Distributed by Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, Made in Ireland, NDC 0069-0469-03. EXPIRATION DATE: September 2021 June 2023
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0826-2021·2021-09-29
Zonisamide Capsules Recalled by Glenmark Due to CGMP Deviations
Glenmark Pharmaceuticals Inc., USA is voluntarily recalling Zonisamide Capsules USP 100 mg nationwide due to CGMP (Current Good Manufacturing Practice) deviations. The recall affects multiple lot numbers distributed from August 2021.
Product
ZONISAMIDE — ZONISAMIDE (ZONISAMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0822-2021·2021-09-29
Glenmark Naproxen Sodium 550 mg Tablets Recalled for CGMP Deviations
Glenmark Pharmaceuticals is recalling specific lots of Naproxen Sodium 550 mg tablets nationwide due to manufacturing deviations. The firm initiated the voluntary recall on August 27, 2021.
Product
NAPROXEN SODIUM — NAPROXEN SODIUM (NAPROXEN SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2487-2021·2021-09-29
SARS-CoV-2 Process Control Swab Recalled Due to Plasmid DNA Contamination
Microbiologics Inc is recalling its SARS-CoV-2 Process Control (Swab) because certain lot numbers were contaminated with plasmid DNA containing SARS-CoV-2 sequences. The affected product was distributed in the United States and internationally.
Product
SARS-CoV-2 Process Control (Swab) - Product Usage: intended for use as an external, non-viable control material to evaluate the performance of nucleic acid tests that detect SARS-CoV-2 virus.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·21V753000·2021-09-28
Tiffin Wayfarer RV Water Tank Mounting Defect Increases Crash Risk
Tiffin Motorhomes is recalling 2018-2022 Wayfarer RVs because the rear water tank mounting bolts can fail, causing the tank to fall onto the exhaust pipe. This affects vehicle stability and increases crash risk.
Product
TIFFIN — TIFFIN WAYFARER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V755000·2021-09-28
2022 Thor Motor Coach Rize Motorhomes Recalled for LP Gas Line Rupture Risk
Thor Motor Coach is recalling 2022 Rize and Scope motorhomes due to an LP gas line that may be too short and improperly installed. A gas leak from a ruptured line could cause a fire.
Product
THOR MOTOR COACH — THOR MOTOR COACH RIZE, SCOPE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V767000·2021-09-28
Entegra Class A Motorhomes Recalled for Fuel Hose Leak Fire Risk
Entegra Coach is recalling certain 2021-2022 Anthem, Aspire, and Reatta XL Class A motorhomes with Cummins diesel engines due to fuel hoses that may leak and pose a fire risk. Owners should contact Entegra customer service at 1-800-283-8267 for free replacement.
Product
ENTEGRA — ENTEGRA ANTHEM, REATTA XL, ASPIRE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V754000·2021-09-28
Thor Motor Coach Omni motorhomes recalled for LP gas line fire hazard
Thor Motor Coach is recalling 2021-2022 Omni and Magnitude motorhomes due to an LP gas line routing defect. The line may be incorrectly routed through the rear suspension leaf springs, potentially causing a gas leak and fire risk.
Product
THOR MOTOR COACH — THOR MOTOR COACH OMNI, MAGNITUDE, redundant MAGNITUDE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V757000·2021-09-28
Rosenbauer Recalls Fire Trucks Due to Improperly Crimped Lifting Cables
Rosenbauer America is recalling specific 2020-2022 fire trucks because improperly crimped lifting cables may detach, causing the generator set to fall and increasing injury risk.
Product
ROSENBAUER — ROSENBAUER COMMANDER, COMMERCIAL HV507, PANTHER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V756000·2021-09-28
Thor Motor Coach Recalls 2021-2022 Venetian Motorhomes for Awning Defect
Thor Motor Coach is recalling 2021-2022 Venetian motorhomes because improperly installed patio awnings may separate while driving, increasing crash risk.
Product
THOR MOTOR COACH — THOR MOTOR COACH VENETIAN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V752000·2021-09-27
Spartan K3 and K4 Recalled for Power Steering Pump Defect
Shyft Group is recalling 2020-2022 Spartan K3 and K4 RVs because a machining defect may cause the power steering pump shaft seal to break, resulting in a loss of power steering assist.
Product
SPARTAN — SPARTAN K4, K3
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V617000·2021-09-27
Toyota Recalls 2019-2020 Yaris Models for Fuel Pump Defect
Toyota is recalling 2019-2020 Yaris vehicles because a fuel pump impeller may crack, potentially causing engine stalls and increasing crash risk.
Product
TOYOTA — TOYOTA YARIS
Category
Vehicle
Distribution
Distributed nationwide