State

Arkansas product recalls

72,820 recalls have nationwide distribution and so reach Arkansas. 5,510 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total: 5,510
Critical: 1,016
Severe: 1,209
Most recent: 2026-09-02

Of the 5,510 recalls naming Arkansas we have scored against our rubric, 1,016 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,209 (22%) are Severe.

Which agencies issued them

These figures cover only the 5,510 recalls whose distribution notice names Arkansas specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

401–425 of 78330

HighFDA (Devices)·Z-2860-2026·2026-08-12
Flow Anesthesia Machines Recalled for Failure to Deliver Anesthetic Agent
The FDA is recalling Flow Anesthesia Machines because events occurred where the anesthetic agent was not delivered when the vaporizer was activated, potentially causing patients to receive insufficient anesthesia.
Product
Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530 Flow-i C40 6888540 Flow-c 6887700 Flow-e 6887900
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2898-2026·2026-08-12
United Orthopedic Recalls U2 Total Knee System Femoral Offset Bushings
United Orthopedic Corp. is recalling U2 Total Knee System femoral offset bushings due to incorrect engraved numbering that could cause incorrect implant orientation.
Product
Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 2mm and 6mm Model/Catalog Number: 9323-5312 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No, N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2839-2026·2026-08-12
Biopsy Forceps Recall: Sterile Packaging Breach Risk
Boston Scientific is recalling Radial Jaw 4 Large Capacity Biopsy Forceps due to a potential breach in the sterile barrier of device packaging, which could compromise sterility.
Product
Radial Jaw 4 Large Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial Jaw 4 LC 240cm Box 20; Outer Box UPN: M00513321; Inner Box UPN: M00513320. 2. Radial Jaw 4 LC 240cm Box 40; Outer Box UPN: M00513322; Inner Box UPN: M00513320. 3. Radial J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2878-2026·2026-08-12
GE Healthcare Portrait Core Services Software Recall Due to Software Vulnerability
GE Medical Systems Information Technologies Inc is recalling GE Healthcare Portrait Core Services SW V 1.2.0 (REF 5700592) patient monitoring systems due to a software vulnerability.
Product
GE Healthcare Portrait Core Services SW V 1.2.0, REF 5700592. patient monitoring system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2886-2026·2026-08-12
United Orthopedic Corp. Recalls Femoral Valgus Offset Adaptors for U2 Total Knee System
United Orthopedic Corp. is recalling specific femoral valgus offset adaptors used in the U2 Total Knee System due to a manufacturing defect in a component screw.
Product
Brand Name: U2 Total Knee System Product Name: Femoral valgus offset adaptor, 2mm, 4mm, 6mm, left and Femoral valgus offset adaptor, 2mm, 4mm, 6mm, right Model/Catalog Number: 9323-5335, 9323-5337, 9323-5339 and 9323-5336, 9323-5338, 9323-5340 Software Version: N/A Product De
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2883-2026·2026-08-12
Knee Prosthesis Trial Recall for Manufacturing Defect
United Orthopedic Corp. recalls U2 Total Knee System PSA Box Trial due to a manufacturing defect in a component screw that prevents proper assembly of the stem trial.
Product
Brand Name: U2 Total Knee System Product Name: PSA Box Trial, L, #1-6 and PSA Box Trial, R, #1-6 Model/Catalog Number: 9323-5511 thru 9323-5516 and 9323-5521 thru 9323-5526 Software Version: N/A Product Description: Knee femur prosthesis trial, reusable Component: No, N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2892-2026·2026-08-12
Philips Azurion interventional fluoroscopic X-ray systems recalled for potential hardware failures
Philips Azurion X-ray systems may lose imaging capability or motor functions due to unauthorized hard drives.
Product
Philips Azurion under the following System Descriptions and corresponding model numbers: 1. Azurion 3 M12; Model Numbers: 722063, 722221. 2. Azurion 3 M15; Model Numbers: 722064, 722222, 722280. 3. Azurion 5 M12; Model Number: 722227. 4. Azurion 5 M20; Model Numbers: 7222
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2863-2026·2026-08-12
Stryker Ahto Tube Set Recalled for Handpiece Leaking During Use
Stryker is recalling 41,052 Ahto Tube Sets worldwide due to reports of handpiece leaking during use.
Product
STRYKER AHTO TUBE SET WITH TIP PACKAGING, Catalog Number 0250070620
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2896-2026·2026-08-12
5-PLASMA Bivalirudin Control Model 5D-44905 Recalled Due to Stability Issues
Aniara Diagnostica LLC is recalling 5-PLASMA Bivalirudin Control (Model 5D-44905) due to stability issues that may cause degradation of measurable bivalirudin.
Product
5-PLASMA Bivalirudin Control, Model Number 5D-44905
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2838-2026·2026-08-12
Boston Scientific Radial Jaw 4 Biopsy Forceps Recalled Due to Sterile Barrier Breach Risk
Boston Scientific Corporation is recalling specific Radial Jaw 4 Standard Capacity Biopsy Forceps because there is a potential for a breach in the sterile barrier of the device packaging.
Product
Radial Jaw 4 Standard Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial Jaw 4 SC 240cm Box 20; Outer Box UPN: M00513401; Inner Box UPN: M00513400. 2. Radial Jaw 4 SC 240cm Box 40; Outer Box UPN: M00513402; Inner Box UPN: M00513400. 3. Radia
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2905-2026·2026-08-12
COAPTIUM CONNECT peripheral nerve repair device recalled due to inaccurate shelf life labeling
The FDA is recalling the COAPTIUM CONNECT peripheral nerve repair device because its shelf life was previously overstated, which could cause device failure during surgery.
Product
Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number: NCOCO3010 Software Version: N/A Product Description: In situ polymerizing peripheral nerve repair device Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2895-2026·2026-08-12
Aniara 5-PLASMA Bivalirudin Calibrator Recalled for Stability Issues
Aniara Diagnostica LLC is recalling 7 units of 5-PLASMA Bivalirudin Calibrator due to stability issues that cause degradation of measurable bivalirudin.
Product
5-PLASMA Bivalirudin Calibrator, Model Number 5D-46905
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2908-2026·2026-08-12
COAPTIUM CONNECT medical device shelf life recalibration recall
TISSIUM SA is recalling COAPTIUM CONNECT devices because their original 36-month shelf life was not supported by real-time data, requiring relabeling to a 26-month shelf life to prevent potential device failure during surgery.
Product
Brand Name: COAPTIUM CONNECT Product Name: COAPTIUM CONNECT Model/Catalog Number: NCOCO6010 Software Version: N/A Product Description: In situ polymerizing peripheral nerve repair device Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0733-2026·2026-08-12
Dicyclomine Hydrochloride Capsules Recalled for Empty Capsules
Aurobindo Pharma is recalling dicyclomine hydrochloride capsules, 10mg, due to reports of empty capsules found in the product.
Product
DICYCLOMINE HYDROCHLORIDE — DICYCLOMINE HYDROCHLORIDE (DICYCLOMINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2881-2026·2026-08-12
Siemens Tricyclic Antidepressant Calibrator/Controls Recall Lot U2
Siemens Healthcare Diagnostics is recalling Lot U2 of its Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls due to an out-of-specification sodium azide concentration. The recall affects 494 units in the US and 114 units overseas, distributed nationwide and internationally.
Product
Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls SMN 10445390 Catalog No. 7C219UL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2910-2026·2026-08-12
Blom-Singer Voice Prosthesis Recalled Due to Incorrect Labeling
Freudenberg Medical recalls 40 Blom-Singer Classic Indwelling Voice Prostheses due to labeling errors that could cause confusion about product contents.
Product
Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm REF: 1610-LF
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2882-2026·2026-08-12
Happiest Baby Recalls Pre-Loved SNOO Smart Sleeper Bassinets
Happiest Baby, Inc is recalling 4 refurbished SNOO Smart Sleeper bassinets (Model S1000) that failed to meet quality standards before distribution. The recall is being reported retroactively.
Product
Happiest Baby, Inc Pre-loved SNOO Smart Sleeper Model:S1000
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2880-2026·2026-08-12
Syva Emit Disopyramide Enzyme Immunoassay Calibrator Recalled for Sodium Azide Concentration
Siemens Healthcare Diagnostics is recalling Syva Emit Disopyramide Enzyme Immunoassay Calibrator Lot U1 due to out-of-specification sodium azide concentration.
Product
Syva Emit Disopyramide Assay Enzyme Immunoassay, Lidocaine SMN 10445370 Catalog No 6N319UL
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V523000·2026-08-10
Daimler Recalls 2024-2027 Thomas Built Buses Saf-T-Liner C2 for Fuel System Defect
Daimler Trucks North America is recalling 2024-2027 Thomas Built Buses Saf-T-Liner C2 transit buses because the fuel tank cage and fuel system mounting may be incompatible, increasing the risk of a fire during a crash.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V520000·2026-08-10
Blue Bird Recalls 2023-2027 Vision Transit Buses for Wiring Defect
Blue Bird is recalling 2023-2027 Vision Transit Buses because a damaged 12V power wire may short circuit, potentially disabling safety lights and increasing crash risk.
Product
BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V522000·2026-08-10
Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Fuel System Defect
Daimler Trucks North America is recalling 2024-2027 Thomas Built Buses Saf-T-Liner C2 school buses because incompatible fuel tank components may cause a fuel leak and fire during a crash.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V521000·2026-08-10
Marion Recalls 2025 Pumper Fire Engines Due to Display Unit Failure
Marion Body Works is recalling 2025 Pumper fire engines because a display unit may fail, preventing the activation of emergency lights and firefighting equipment.
Product
MARION — MARION PUMPER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V519000·2026-08-10
Blue Bird Recalls Vision School Buses Over Electrical Short Circuit Risk
Blue Bird is recalling certain Vision School Buses because a 12V power wire may short circuit, disrupting rear lighting or warning lights and increasing crash risk. Dealers will repair free.
Product
BLUE BIRD — BLUE BIRD VISION SCHOOL BUS, VISION SCHOOL BUS (ELECTRIC)
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-08082026-01·2026-08-08
Meat and poultry products containing recalled jalapeños may contain Salmonella
The USDA FSIS is issuing a public health alert for various meat and poultry products that contain FDA-regulated jalapeños potentially contaminated with Salmonella.
Product
FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Jalapeños That Have Been Recalled Due To Possible Salmonella Contamination
Category
Food
Distribution
Distributed nationwide
HighUSDA FSIS·015-2026·2026-08-08
City Foods, Inc. Recalls Pastrami and Corned Beef Due to Listeria Risk
City Foods, Inc. is recalling approximately 3,215 pounds of ready-to-eat pastrami and corned beef products because they may be contaminated with Listeria monocytogenes.
Product
City Foods, Inc./Bea's Best Corned Beef — City Foods, Inc. Recalls Ready-To-Eat Pastrami and Corned Beef Products Due To Possible Listeria Contamination
Category
Food
Distribution
Distributed nationwide