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.

24901–24925 of 79052

HighFDA (Devices)·Z-2466-2021·2021-09-22
BD Alaris Infusion Pump Buerette Set Connector Valve Occlusion Issues
BD Alaris needle-free connector valves in Buerette Sets may develop occlusions, difficulty flushing, or flow issues that could delay patient therapy. The product was distributed worldwide across all US states and multiple countries.
Product
BD Alaris Pump Infusion Buerette Set Smallbore Tubing Smartsite Port (Burette) 3 SmartSite Y-Sites, REF: 2441-0006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2453-2021·2021-09-22
Configura Advance Mobility Chairs Recalled for Potential Backrest Detachment
Accora Inc is recalling multiple Configura Advance Chair models due to a potential defect where the backrest may detach, creating a fall risk for users.
Product
Configura Advance Chair, Model Number: CHAIR-0-SC1-030; Advance Chair, 100mm Castors, Std Backrest, Manual; Serial Numbers: 10001-SC1-20 to 10483-SC1-20; 10001-SC1-21 to 10224-SC1-21; 10231-SC1-21 to 10456-SC1-21; 10481-SC1-21 to 10570-SC1-21. Model Number: CHAIR-0-SC2-030…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0794-2021·2021-09-22
Oxycodone Hydrochloride Tablets Recalled for Foreign Tablet Contamination
Rhodes Pharmaceuticals is recalling Oxycodone Hydrochloride 10 mg tablets (Lot # WP5K0Y) distributed nationwide after a foreign Hydrochlorothiazide/Lisinopril tablet was found in one bottle.
Product
OXYCODONE HYDROCHLORIDE — OXYCODONE HYDROCHLORIDE (OXYCODONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2447-2021·2021-09-22
MR MAGNETOM Imaging Systems Risk Data Loss in Treatment Planning
Siemens MR MAGNETOM imaging systems may lose treatment planning data when editing structure sets after reopening a saved study, resulting in incomplete treatment plans being transmitted to planning systems.
Product
MR MAGNETOM Systems with RT Image Suite with syngo MR VA20A, VA30A and VA31A with license SW-Key CT_RT_IMA_SUITE_SYNTHETIC_CT Material Numbers: 11060815
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2464-2021·2021-09-22
Needle-Free Burette Set Valves Recalled for Occlusion and Flow Issues
BD ADD-ON Burette Set V/NV Needle-Free Valves may experience occlusions or flow issues that could delay therapy. CAREFUSION recalled 44,120 units with this defect.
Product
BD ADD-ON Burette Set V/NV Needle-Free Valve, REF: 82113E-0006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2459-2021·2021-09-22
BD Alaris Infusion Pump Buerette Sets Needle-Free Connector Valve Issues
BD Alaris Pump Infusion Buerette Sets with needle-free connector valves may experience flushing difficulties, flow issues, or occlusions that could delay therapy delivery. No illnesses or injuries have been reported.
Product
BD Alaris Pump Infusion Buerette Set 0.2 Micron Filter Smallbore Tubing SmartSite Port (Burette) SmartSite Y-Site, REF: 10015012; BD Alaris Pump Infusion Buerette Set Ball Valve Smallbore Tubing Smartsite Port (Burette) SmartSite Y-Site, REF: 10817920; BD Alaris Pump Infusion…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2448-2021·2021-09-22
Pentax Medical Colonoscopes and Upper GI Scopes Updated Reprocessing Instructions
Pentax is updating reprocessing instructions for over 28,000 colonoscopes and Upper GI scopes distributed nationwide between 2014 and 2021. Healthcare facilities should implement the updated procedures provided by the manufacturer.
Product
Colonoscope Family # 1-Pentax Video Colonoscopes (EC Family) with One Instrument Channel and a Water Jet Channel Models: EC-2990Li, EC-3490Li, EC-3890Li, EC-3490TLi, EC-3490LK, EC-3890LK, EC3890LZi, EC34-i10L, EC38-i10L; Colonoscope Family # 2-Pentax Video Colonoscopes with…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2477-2021·2021-09-22
Lyra Direct SARS-CoV-2 Assay Instructions Revised for False Negative Risk
The Lyra Direct SARS-CoV-2 assay can produce false negatives on certain PCR machines when specimens have high viral loads. Revised instructions address this diagnostic failure risk affecting approximately 81,910 kits distributed worldwide.
Product
Lyra Direct SARS-CoV-2 Assay Emergency Use Authorization- Ref: M124. The Lyra Direct SARS-CoV-2 Assay is a real-time RT-PCR assay intended for the qualitative detection of nucleic acid from SARS-CoV-2 in nasal (NS), nasopharyngeal (NP), or oropharyngeal (OP) direct swab…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2452-2021·2021-09-22
Cellex COVID-19 Antigen Test kits recalled for lacking FDA emergency use authorization
Cellex is recalling approximately 44,821 units of its qSARS-CoV-2 Antigen Rapid Test due to lack of FDA emergency use authorization. The test was distributed nationwide in California, Florida, Texas, and Wisconsin.
Product
Cellex qSARS-Cov-2 Antigen Rapid Test, 25 tests/box, submitted as EUA202955 "declined to issue"
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2454-2021·2021-09-22
Extension Set SMALLBORE Tubing with SmartSite Valves Recalled for Flushing Issues
BD Extension Set SMALLBORE Tubing with SmartSite Valves (REF: 20019E) is being recalled due to flushing difficulties, flow issues, and occlusions that could delay therapy. Over 1.4 million units distributed worldwide are affected.
Product
BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2462-2021·2021-09-22
BD Gravity Burette Set Needle-Free Connector Valves Recalled for Flow Issues
CAREFUSION is recalling BD Gravity Burette Sets with needle-free connector valves that may develop flow restrictions and blockages, potentially delaying medication delivery. Approximately 29,130 units were distributed.
Product
BD Gravity Burette Set 60 DP 3 SmartSite VALVES BALL VALVE DRIP CHAMBER, REF: 10012564
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2463-2021·2021-09-22
BD Gravity IV needle-free connector valve occlusion risk
BD Gravity IV needle-free connector valves may develop flow issues and partial or total occlusions that could delay therapy. The recall affects 24,360 units distributed worldwide.
Product
BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free Y-sites, REF: CM42500E-07; BD Gravity IV Set 3-port Closed Stopock Manifold Back Check Valve 2 Needle-Free Y-sites, REF: CS42522E-07; BD GRAVITY 10 DP V/NV CHECK VALVE 3-WAY STOPCOCK 4 Smartsite VALVES &…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2445-2021·2021-09-22
Radiation Therapy Software Risk: Data Loss in Treatment Planning
Siemens radiation therapy planning software may lose data when editing treatment structures. Incomplete structure sets could be sent to the treatment planning system, affecting treatment plan accuracy.
Product
syngo.via RT Image Suite with syngo.via VB30, VB40, VB50 and VB60- Intended for Radiation Therapy Treatment Material Number: 10496180
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2471-2021·2021-09-22
Siemens ACUSON Juniper ultrasound system recalled for intermittent power supply failure
Siemens Medical Solutions USA is recalling 15 ACUSON Juniper Diagnostic Ultrasound Systems worldwide due to intermittent power supply failures that render the devices inoperable. No injuries or illnesses have been reported.
Product
ACUSON Juniper Diagnostic Ultrasound System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2474-2021·2021-09-22
Philips Allura Xper X-ray imaging system failures at 480V power supply
Four Philips Allura Xper X-ray imaging systems may fail prematurely when powered at 480V hospital mains, causing coil overheating and reduced imaging performance.
Product
The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. This includes, e.g., peripheral, cerebral, thoracic and abdominal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2468-2021·2021-09-22
BD Needle-Free Bag Access Valves Recalled for Flow Obstruction
BD SmartSite needle-free valves may become obstructed, preventing proper fluid flow in medical infusions. The FDA recalls over 295,000 units due to risk of therapy delays.
Product
BD SmartSite Bag Access Device Needle-Free Valve, REF: 2300E; BD Bag access Device with 1 Check Valve And Needle Free Valve, REF: 2309E-0006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2475-2021·2021-09-22
Philips Allura Xper Imaging System Overheating and Malfunction Recall
Philips Allura Xper imaging systems may fail early when supplied with 480V, causing coil overheating and burning smell. When the system fails, X-ray imaging capability is reduced to emergency mode only.
Product
The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. This includes, e.g., peripheral, cerebral, thoracic and abdominal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2451-2021·2021-09-22
FDA Recalls Luminex Verigene Enteric Pathogen Test Kits for False Positive Results
Luminex Corporation is recalling 4,579 Verigene EP Amplification Reagent Kit Test units worldwide due to potential for false positive results. Affected kits distributed across the United States, Austria, France, Greece, Japan, and Turkey may produce incorrect test results.
Product
Verigene EP Amplification Reagent Kit Test
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2458-2021·2021-09-22
BD needle-free connector valves may occlude or restrict fluid flow
BD Burette Gravity Set needle-free connector valves may fail to flush or develop blockages, potentially delaying patient therapy. Lot 21015553 consists of approximately 630 units distributed worldwide.
Product
BD BURETTE GRAVITY SET 60 DROP 2 Smartsite VALVES VENTED/NONVENTED, REF: 42163E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2461-2021·2021-09-22
BD SmartSite Bag Access Device Recalled for Valve Occlusion Issues
CAREFUSION is recalling BD SmartSite Bag Access Device needle-free connector valves due to potential occlusions and flow issues that could delay therapy delivery.
Product
BD SmartSite Bag Access Device, REF: 2300E-0500; BD BAG ACCESS DEVICE CHECK VALVE SmartSite VALVE, REF: 2309E
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V735000·2021-09-22
2020-2021 Ford Explorer and Lincoln vehicles rearview camera display failure
Ford and Lincoln are recalling 228,297 vehicles with 360-degree cameras because the rearview camera image may fail to display, reducing rear visibility and increasing crash risk.
Product
FORD — FORD, LINCOLN EXPLORER, AVIATOR, CORSAIR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V734000·2021-09-22
2022 Toyota Prius engine control software may disable hybrid system
Toyota is recalling 2022 Prius and Prius Prime vehicles whose Engine Control Unit software may falsely trigger shutdown of the hybrid system, causing loss of drive power. Contact Toyota at 1-800-331-4331 for a free software update.
Product
TOYOTA — TOYOTA PRIUS PRIME, PRIUS
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2481-2021·2021-09-22
Leica BOND Primary Antibody CDX2 Recalled for Performance Specification Issue
Leica Microsystems recalls BOND Ready-To-Use Primary Antibody CDX2 (PA0375, Lot 69909) because the product may not perform as specified in its instructions for use. The recall affects 237 units distributed nationwide.
Product
BOND Ready-To-Use Primary Antibody CDX2 (EP25), REF PA0375
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0801-2021·2021-09-22
Glycopyrrolate Injection Recalled for Failed Impurities and Degradation Specifications
Meitheal Pharmaceuticals is recalling Glycopyrrolate Injection, USP 4mg per 20mL in 20mL multi-dose vials due to failed impurities and degradation specifications. The recall affects specific lots distributed nationwide in the USA and India.
Product
Glycopyrrolate Injection, USP 4mg per 20mL, 20 mL Multi-Dose Vials, Rx only, Mfd for Meitheal Pharmaceuticals, Chicago, IL 60631. NDC 71288-408-21
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0802-2021·2021-09-22
Betamethasone Dipropionate Lotion recalled for unknown impurity
Akorn, Inc. is recalling Betamethasone Dipropionate Lotion USP (Augmented), 0.05%, due to an unknown impurity found in the product that exceeds specification limits. The affected lots were distributed nationwide.
Product
Betamethasone Dipropionate Lotion USP (Augmented), 0.05%, packaged in a) 30 mL bottle (NDC 61748-480-30), b) 60 mL bottle (NDC 61748-480-60), Rx only, Manufactured by: Hi-Tech Pharmacal Co. Inc., Amityville,NY 11701
Category
Drug
Distribution
Distributed nationwide