State

Arkansas product recalls

72,919 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 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2576–2600 of 78432

HighFDA (Food)·H-0639-2026·2026-04-08
Dumpling Party Tray Products Recalled for Glass Fragments
JFE Franchising Inc is recalling three dumpling products due to possible glass fragments. Affected products include Dumpling Party Tray (20pcs and 40pcs) Vegetable varieties and Cheetos Flamin Hot Loaded Dumpling Vegetable.
Product
" Dumpling Party Tray (20pcs) Vegetable 13 oz 011110661173 " Dumpling Party Tray (40pcs) Vegetable 26 oz 011110661180 " Cheetos Flamin Hot Loaded Dumpling Vegetable 6oz 011110663474
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-1761-2026·2026-04-08
Burlington Medical leg wraps may lose radiation attenuation over time
Burlington Medical is recalling leg wraps because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
Product
Burlington Medical, Leg Wraps.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1672-2026·2026-04-08
Philips Allura Xper FD20/15 OR Table X-ray may not start
Philips is recalling the Allura Xper FD20/15 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/15 OR Table; System Code: 722059;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0638-2026·2026-04-08
Dumpling and Loaded Dumpling Vegetable products recalled for glass contamination
JFE Franchising Inc is recalling Dumpling Vegetable and Loaded Dumpling Vegetable products due to the presence of glass fragments. The products were distributed across multiple U.S. states.
Product
" Dumpling Vegetable 4.5 oz 011110658067 " Loaded Dumpling Vegetable 5.7 oz 011110696953
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-1708-2026·2026-04-08
Medline endoscopy kits contain recalled Olympus biopsy valves shedding fragments
Medline is recalling BAL and ENDO kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1691-2026·2026-04-08
Medline ENFit G-tube connector kits may leak from dimensional defect
Medline is recalling kits containing ENFit G-tube connectors because the connectors were not made to required dimensional specifications and may not form a proper seal.
Product
Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT 2. SKU ENFITDISCKIT ENFIT DISCHARGE KIT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1706-2026·2026-04-08
Medline bronchoscopy packs contain recalled Olympus biopsy valves shedding fragments
Medline is recalling three bronchoscopy convenience kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Medline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK, DYKE2096 2. NON MB BRONCHOPSCOPY CCH LH PK, DYNJT6182 3. PULMONARY BRONCH PACK, DYNDA2861A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1752-2026·2026-04-08
Paradigm REAL-Time Veo pump delivery varies with pump height changes
Medtronic is recalling Paradigm REAL-Time Veo insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
Paradigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1694-2026·2026-04-08
Olympus SOLTIVE Premium laser power supply may fail producing smoke
Olympus is recalling SOLTIVE Premium SuperPulsed Laser Systems because a potential defect in the 24V power supply module may render the system inoperable and produce smoke or a burning smell.
Product
Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS Model/Catalog Number: TFL-PLS containing TFL-CPLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1762-2026·2026-04-08
Burlington Medical half aprons may lose radiation attenuation over time
Burlington Medical is recalling half aprons because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
Product
Burlington Medical, Half Aprons.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1749-2026·2026-04-08
Paradigm REAL-Time insulin pump delivery varies with pump height
Medtronic is recalling Paradigm REAL-Time insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1711-2026·2026-04-08
Medline anterior hip pack contains recalled Olympus biopsy valves
Medline is recalling the Anterior Hip Pack because it contains recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
MEDLINE ANTERIOR HIP PACK DYNJ64672B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1743-2026·2026-04-08
MiniMed 640G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 640G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1747-2026·2026-04-08
MiniMed 620G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 620G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 620G Insulin Pump (MMT-1750)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1665-2026·2026-04-08
Philips Allura Xper FD20 OR Table X-ray may not start
Philips is recalling the Allura Xper FD20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1670-2026·2026-04-08
Philips Allura Xper FD20/20 OR Table X-ray may not start
Philips is recalling the Allura Xper FD20/20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/20 OR Table; System Code: 722039;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0415-2026·2026-04-08
Rugby and Walgreens lubricant eye drops recalled over sterility assurance
K.C. Pharmaceuticals is recalling Sterile Eye Drops Soothing Tears, sold as Rugby Lubricating Eye Drops and Walgreens Lubricant Eye Drops, for lack of assurance of sterility.
Product
STERILE EYE DROPS SOOTHING TEARS (polyethylene glycol 400 0.4% and propylene glycol 0.3%), 0.5 OZ 0.5 fl oz (15 mL) bottles; a) Rugby LUBRICATING EYE DROPS, Distributed by: Rugby Laboratories, Livonia, MI 48152, NDC 0536-1219-94; b) Walgreens, Lubricant Eye Drops, DISTRIBUTED BY
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1703-2026·2026-04-08
VOLT bone taps swapped between lots carry the incorrect thread
The 2.4 VOLT Tap Cortex Screw is being recalled after a full lot swap with the VOLT Locking Screw Tap left the bone taps with an incorrect thread.
Product
2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1739-2026·2026-04-08
MiniMed 670G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 670G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0409-2026·2026-04-08
Quality Choice irritation relief eye drops recalled over sterility assurance
Quality Choice Eye Drops Irritation Relief, containing tetrahydrozoline HCl and zinc sulfate, are being recalled for lack of assurance of sterility. 182,424 bottles are affected.
Product
QUALITY CHOICE EYE DROPS IRRITATION RELIEF — QUALITY CHOICE EYE DROPS IRRITATION RELIEF (TETRAHYDROZOLINE HCL, ZINC SULFATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1745-2026·2026-04-08
MiniMed 720G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 720G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1661-2026·2026-04-08
Philips Allura Xper FD10 X-ray may not start from foot switch
Philips is recalling the Allura Xper FD10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0421-2026·2026-04-08
Prazosin hydrochloride further lots recalled over nitrosamine impurity levels
A further quantity of Prazosin Hydrochloride tablets is being recalled after detection of the nitrosamine impurity N-nitroso-prazosin impurity C above acceptable limits.
Product
PRAZOSIN HYDROCHLORIDE — PRAZOSIN HYDROCHLORIDE (PRAZOSIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1679-2026·2026-04-08
Philips Azurion 5 M12 X-ray may not start from foot switch
Philips is recalling the Azurion 5 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 5 M12; System Code: (1)722227, (2)722231;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1659-2026·2026-04-08
Philips Allura Xper FD10C X-ray may not start from foot switch
Philips is recalling the Allura Xper FD10C because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD10C; System Code: 722001;
Category
Medical Device
Distribution
Distributed nationwide