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. 2,451 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,451 in last 12 months

Showing 2720127220 of 28,355 recalls

Medical DeviceSeptember 20, 2012· Sorin Group USA, Inc.

Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Brivo XR 285 Mobile general purpose radiographic imaging...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Captiva Spine, Inc

Recalled Item: CapLOX II Final Torque Driver Recalled by Captiva Spine, Inc Due to Captiva...

The Issue: Captiva Spine recalled their CapLOX II Final Torque Driver, Indicator due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 220amx Mobile general purpose radiographic imaging...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Sorin Group USA, Inc.

Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima 200amx Mobile general purpose radiographic imaging of...

The Issue: It was discovered GE Healthcare has become aware of a firmware issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Advanced Sterilization Products

Recalled Item: STERRAD NX Cassettes Recalled by Advanced Sterilization Products Due to...

The Issue: Advanced Sterilization Products is recalling three lots of STERRAD NX System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Medline Industries Inc

Recalled Item: Medline Total Knee CDS Recalled by Medline Industries Inc Due to The Back...

The Issue: The Back Table Cover component in the custom pack was placed in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA ML Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...

The Issue: Horiba Medical is recalling ABX PENTRA ML because they have confirmed an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware that patient mismatch without a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Double Roller Pump 85 Recalled by Sorin Group USA, Inc. Due to Sorin...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Cure Medical LLC

Recalled Item: Male Recalled by Cure Medical LLC Due to The firm initiated the product...

The Issue: The firm initiated the product recall because labeling on some of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: Sorin C5 Perfusion System Recalled by Sorin Group USA, Inc. Due to Sorin...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Mast Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Single Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Trumpf Medical Systems, Inc.

Recalled Item: Helion and Xenion surgical lights Recalled by Trumpf Medical Systems, Inc....

The Issue: Incidents regarding fractures of the front joint of the spring arm have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Mast Roller Pump 85 Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by...

The Issue: The low contrast pins in the Image Quality (IQ) phantom deteriorates over...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Elekta, Inc.

Recalled Item: MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR)...

The Issue: A patient was seriously mistreated after a user made and saved an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Instratek, Incorporated

Recalled Item: Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The...

The Issue: Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger...

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

Class II — Potential Health HazardOngoing