State

Arkansas product recalls

73,596 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: 1,027
Severe: 1,448
Most recent: 2026-10-14

Of the 5,543 recalls naming Arkansas we have scored against our rubric, 1,027 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,448 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,543 recalls whose distribution notice names Arkansas specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28276–28300 of 79139

HighFDA (Devices)·Z-0520-2021·2020-12-09
K2M Recalls Yukon Anti-Torque Alignment Tubes Due to Manufacturing Defect
K2M, Inc. is recalling four Yukon Anti-Torque Alignment Tubes from Lot KTGG because shafts do not pass through the inner cannula, potentially delaying surgery.
Product
Yukon OCT Spinal System Yukon Anti-Torque Alignment Tube - Product Usage: The Anti-Torque Alignment Tube (the Alignment Tube ) provides counter rotation to reduce the torque applied to the anatomy when the size 15 Torque limiting shaft (the shaft is used to tighten the Yukon…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0499-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Product
Olympus Ultrasound Endoscope, Model Number: GF-UCT140-AL5 - Product Usage: used with other supporting equipment for endoscopic real-time ultrasound imaging and endoscopic surgery within the gastrointestinal tract.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0503-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Product
Olympus Ultrasound Endoscope, Model number: GF-UMQ130 - Product Usage: used with an Olympus Endoscopic Ultrasound Center, EVIS Video System Center, light source, documentation equipment, video monitor, Endo-Therapy accessories and other ancillary equipment for endoscopic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0500-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Updated Cleaning Instructions
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Product
Olympus Ultrasound Endoscope, Model number: GF-UCT180 - Product Usage: used with an Olympus universal endoscopic ultrasound center or a diagnostic system (ALOKA CO. LTD), video system center, light source, documentation equipment, monitor, EndoTherapy accessories and other…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0528-2021·2020-12-09
CME America Recalls Neofeed Syringe Pumps Due to Motor Wear and Cracks
CME America is recalling 4,182 Neofeed syringe pumps because motor wear may cause under-infusion without alarms and cracks may allow cleaning fluids to damage hardware.
Product
CME America T-Syringe Pump - Neofeed - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21043·2020-12-09
Spirit Halloween Recalls Children's Flashlights Due to Fire and Burn Hazards
Spirit Halloween is recalling about 6,100 children's flashlights because the batteries can overheat, posing fire and burn hazards.
Product
Children's flashlights
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0498-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Infection Risk Mitigation
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Product
Olympus Ultrasound Endoscope, Model number: GF-UCT140P-AL5 - Product Usage: used with other supporting equipment for endoscopic real-time ultrasound imaging and endoscopic surgery within the gastrointestinal tract.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21048·2020-12-09
Washington Shoe Company Recalls Western Chief Toddler Rain Boots Due to Choking Hazard
Washington Shoe Company is recalling Western Chief toddler light-up rain boots because rivets on the handles can detach, posing a choking hazard to children.
Product
Western Chief toddler light-up rain boots
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0532-2021·2020-12-09
Canon Flat Panel Monitor Recall Due to Cable Breakage Risk
Canon Medical System is recalling 14 CAS-930A Flat Panel Monitors because the cable may break during procedures, potentially causing delays or vessel damage.
Product
CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Canon Interventional Angiography System, Model numbers: Infinix-8000C and Infinix-8000H - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V761000·2020-12-09
2021 BMW vehicles recalled for defective 48-Volt battery connections
BMW is recalling certain 2021 model vehicles due to improper assembly of the 48-Volt battery and starter-generator connection, which can increase electrical resistance and fire risk. Dealers will inspect and replace the connection if necessary.
Product
BMW — BMW X5, 530I, X6, X7
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21049·2020-12-09
GrillBlazer Recalls Propane Torch Guns Due to Fire Hazard
GrillBlazer is recalling Su-VGun and GrillGun propane torch guns because propane gas can leak, posing a fire hazard. No injuries have been reported.
Product
Su-VGun and GrillGun propane torch guns
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·21045·2020-12-09
Burley Recalls Dash X FM Child Bicycle Seats Due to Crash Hazard
Burley is recalling Dash X FM child bicycle seats because the reclining plate can detach, making the seat unstable and causing a crash hazard.
Product
Dash® X FM child bicycle seats
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0530-2021·2020-12-09
CME America T-Syringe Pump T34 Recalled for Motor Wear and Hardware Cracks
CME America is recalling 4,182 T-Syringe Pump T34 units because motor wear may cause silent under-infusion and cleaning fluids may crack hardware.
Product
CME America T-Syringe Pump - T34 - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20E090000·2020-12-09
Ford F-250 and F-350 pickup trucks recalled for potential steering lock-up
Icon Vehicle Dynamics is recalling Ford F-250 and F-350 pickup trucks sold with its centerline stabilizer kit. The foam ring in the shock assembly may block piston ports, causing steering to lock up and increasing crash risk.
Product
FORD — FORD F-350 SD, F-250 SD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0504-2021·2020-12-09
Olympus Ultrasound Endoscope Recall for Infection Risk
Olympus is recalling ultrasound endoscopes to reduce the risk of patient infections by adding a new inspection step to the cleaning instructions.
Product
Olympus Ultrasound Endoscope, Model number: GF-UM160 - Product Usage: used for diagnostic ultrasound imaging or fluid flow analysis of the human body.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0515-2021·2020-12-09
Capnostream 35 Portable Respiratory Monitor Recalled for False Temperature Display
Covidien LLC is recalling 3,217 Capnostream 35 Portable Respiratory Monitors because they may display a false 'Temperature Exceeds Limits' message and shut down without an alarm.
Product
Capnostream 35 Portable Respiratory Monitor, Product numbers PM35MN02, PM35MN01, PM35MN05, DLPM35MN02 - Product Usage: use during both no motion and motion conditions and for patients who are well or poorly perfused.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0112-2021·2020-12-09
Golden State Medical Supply Recalls Aripiprazole Tablets for Dissolution Concerns
Golden State Medical Supply is recalling Aripiprazole 15 mg tablets due to potential out-of-specification dissolution limits.
Product
ARIPIPRAZOLE TABLETS, 15 mg, 30-count. bottles, Rx Only, GSMS Incorporated, Manufactured by: Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS, Incorporated, Camarillo, CA 93012 USA, NDC #60429-449-30
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0511-2021·2020-12-09
ICU Medical Recalls IV Administration Sets with Incorrect Filter Assemblies
ICU Medical is recalling 1,100 units of smallbore IV administration sets due to incorrect filter assemblies. The products were distributed nationwide.
Product
REF MC330209 6' (15 cm) Appx 0.09 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, 0.2 Micron Filter, 1.2 Micron Filter, 3 Clamps (Blue, Yellow, White), Rotating Luer - Product Usage: The intravascular administration set is a single use, sterile, non-pyrogenic device, which…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0522-2021·2020-12-09
Chromsystems Recalls MassChrom Cortisol Saliva Control Level I Vials
Chromsystems is recalling 880 vials of MassChrom Cortisol, Cortisone Saliva Control Level I because the control lots may not meet stability criteria, potentially causing increased patient results.
Product
MassChrom Cortisol, Cortisone Saliva Control Level I, Order No. 0349 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0519-2021·2020-12-09
Bausch & Lomb Recalls Toric Intraocular Lenses Due to Missing Axis Marks
Bausch & Lomb is recalling 31 MX60ET toric intraocular lenses because they may be missing toric axis marks, which are necessary for proper surgical placement.
Product
MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric Model MX60ET - Product Usage: The lens is intended for placement in the capsular bag.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0114-2021·2020-12-09
Harvard Drug Group Recalls Aripiprazole Tablets for Dissolution Failure
The Harvard Drug Group is recalling 841 cartons of Aripiprazole Tablets, 15 mg, because the product failed to meet dissolution specifications.
Product
Aripiprazole Tablets, USP, 15 mg, 30 tablets per unit dose carton, Rx Only, Manufactured by: Apotex, Inc, Toronto, Ontario Canada M9L 1T9, Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 USA, NDC 0904-6512-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0524-2021·2020-12-09
ROi CPS Recalls Labor and Delivery Kits Due to Labeling Error
ROi CPS LLC is recalling 220 labor and delivery kits because of an incorrect expiration date on the label.
Product
Regard - Product Usage: Obstetric Gynecologic specialized manual instrument. Labor and delivery kits.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0508-2021·2020-12-09
BD Ultra-Fine Pen Needles Recalled for Incorrect US Labeling
Becton Dickinson is recalling 2.8 million BD Ultra-Fine Pen Needles because US cartons are missing specific compatibility information.
Product
BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for parenteral administration of a drug from a cartridge contained in a drug pen injector Catalog Number: 320122
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0521-2021·2020-12-09
Chromsystems Saliva Calibrator Set Recalled for Stability Issues
Chromsystems is recalling 6PLUS1 Multilevel Saliva Calibrator Sets because they may not meet stability criteria, potentially causing increased cortisone results in patient samples.
Product
6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva, Order No. 73039 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0523-2021·2020-12-09
Chromsystems Recalls MassChrom Cortisol and Cortisone Saliva Control Level II Kits
Chromsystems is recalling MassChrom Cortisol, Cortisone Saliva Control Level II kits because control lots may not meet stability criteria, potentially causing increased results for patient cortisone samples.
Product
MassChrom Cortisol, Cortisone Saliva Control Level II, Order No. 0350 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.
Category
Medical Device
Distribution
Distributed nationwide