Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,666 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,666 in last 12 months

Showing 241260 of 28,355 recalls

Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT...

The Issue: To remove the software applications from certain CT systems as the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm Recalled...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Tornier, Inc

Recalled Item: TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE Recalled by...

The Issue: A specific lot of screws is incorrectly labeled. Screws are labeled as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: NAEOTOM Alpha Software applications: syngo.CT Brain Quantification syngo.CT...

The Issue: To remove the software applications from certain CT systems as the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm Recalled...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification...

The Issue: To remove the software applications from certain CT systems as the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000F Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000H Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000V Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000C Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· ICU Medical, Inc.

Recalled Item: Tego Connector: Recalled by ICU Medical, Inc. Due to Needle free access...

The Issue: Needle free access device intended as accessory to vascular access used in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Tyber Medical

Recalled Item: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column...

The Issue: The supplier manufactured anatomical left plates with an incorrect thread...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Tyber Medical

Recalled Item: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column...

The Issue: The supplier manufactured anatomical left plates with an incorrect thread...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: VANTAGE GALAN 3T Model MRT-3020/MEXL-3020 Recalled by Canon Medical System,...

The Issue: There is a potential for formation of ice occurring in the venting system of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· ICU Medical Inc.

Recalled Item: Pulsator Arterial Blood Sampling Kit Recalled by ICU Medical Inc. Due to...

The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: VANTAGE TITAN 3T Model MRT-3010/MEXL-3010 Recalled by Canon Medical System,...

The Issue: There is a potential for formation of ice occurring in the venting system of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· ICU Medical Inc.

Recalled Item: Portex Spinal Tray Recalled by ICU Medical Inc. Due to Affected lots of...

The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Vascutek, Ltd.

Recalled Item: Gelsoft Plus Recalled by Vascutek, Ltd. Due to Gelatin sealed woven...

The Issue: Gelatin sealed woven polyester prostheses devices, designed for vascular...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing