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. 2,591 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,591 in last 12 months

Showing 1512115140 of 49,990 recalls

DrugJune 8, 2021· Bausch Health Companies, Inc.

Recalled Item: Phytonadione Tablets Recalled by Bausch Health Companies, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodJune 8, 2021· Beechnut Nutrition

Recalled Item: Beech-Nut brand Single Grain Rice Baby Cereal Recalled by Beechnut Nutrition...

The Issue: Product may contain elevated levels of inorganic arsenic (above 100ppb)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: 728333 Spectral CT 7500 -Computed Tomography X-ray system Recalled by...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: 728332 IQon Spectral CT-Computed Tomography X-ray system Recalled by Philips...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: 728327 Ingenuity CT Upgrades-Computed Tomography X-ray system Recalled by...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: 728306 Brilliance iCT-Computed Tomography X-ray systems 728305 Brilliance...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2021· Philips North America Llc

Recalled Item: Model 728321/728323 CT5000 Ingenuity Plus/Pro/Premium-Computed Tomography...

The Issue: When setting patient weight unit preferences to pounds, SynchRight P3T...

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

Class II — Potential Health HazardOngoing
DrugJune 4, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications: due to presence of ATV cyclo...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodJune 4, 2021· Bomunity Ltd Co

Recalled Item: Paximune Dietary Supplement Contains Bovine Proteins that help Promote...

The Issue: Potential to be contaminated with bacteria

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 4, 2021· Simpleware Product Group, SYNOPSYS NORTHERN EUROPE

Recalled Item: Simpleware ScanIP software. For transfer of imaging information from a...

The Issue: A issue (bug) has been identified with the interface and image software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2021· Simpleware Product Group, SYNOPSYS NORTHERN EUROPE

Recalled Item: Simpleware ScanIP medical software. For transfer of imaging information from...

The Issue: A issue (bug) has been identified with the interface and image software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2021· Eight Medical International BV

Recalled Item: Recirculator 8.0s Disposable Lavage Kit (product code number 8100) Recalled...

The Issue: The patient may be exposed to potential aluminum ion release during warming...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Driveline Extension Cable Recalled by Heartware, Inc. Due to...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX Powered Plus Stapler-intended for transection Recalled by...

The Issue: Mislabeled: Labeled on the package as 60mm contains 45mm devices

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Outflow Graft Recalled by Heartware, Inc. Due to Medtronic is...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Accessories Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Driveline Extension Cable Recalled by Heartware, Inc. Due to...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2021· Heartware, Inc.

Recalled Item: HeartWare HVAD Pump Implant Kit Recalled by Heartware, Inc. Due to Medtronic...

The Issue: Medtronic is stopping the distribution and sale of the HVAD System due to a...

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

Class I — Serious Health HazardOngoing