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. 2,623 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,623 in last 12 months

Showing 94419460 of 49,990 recalls

Medical DeviceApril 10, 2023· Wright Medical Technology, Inc.

Recalled Item: stryker ORTHOLOC 3Di Fusion Plate MTP Right Recalled by Wright Medical...

The Issue: Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2023· Wright Medical Technology, Inc.

Recalled Item: stryker ORTHOLOC 3Di Fusion Plate MTP Right Recalled by Wright Medical...

The Issue: Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion...

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

Class II — Potential Health HazardOngoing
DrugApril 7, 2023· Methapharm Inc

Recalled Item: Pantoprazole sodium for Injection 40 mg*/vial Recalled by Methapharm Inc Due...

The Issue: CGMP Deviations; The impacted product and lot number was inadvertently...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 7, 2023· Mondi Lamex Serbia

Recalled Item: Savor Imports IQF Whole Raspberries Recalled by Mondi Lamex Serbia Due to...

The Issue: Potential contamination with Hepatitis A

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 7, 2023· Cytrellis Biosystems, Inc.

Recalled Item: Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring...

The Issue: Irregular core patterns could cause potential overlap of cores at the 8%...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2023· Cook Incorporated

Recalled Item: Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray Recalled by...

The Issue: There were reports from customers that the tracheostomy in the sets and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 7, 2023· Cook Incorporated

Recalled Item: Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set Recalled by...

The Issue: There were reports from customers that the tracheostomy in the sets and...

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

Class I — Serious Health HazardOngoing
DrugApril 6, 2023· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Simvastatin USP Recalled by PD-Rx Pharmaceuticals, Inc. Due to CGMP deviations.

The Issue: CGMP deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2023· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Glimepiride USP Recalled by PD-Rx Pharmaceuticals, Inc. Due to CGMP deviations.

The Issue: CGMP deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2023· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Montelukast Sodium USP Recalled by PD-Rx Pharmaceuticals, Inc. Due to CGMP...

The Issue: CGMP deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2023· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Simvastatin USP 20 mg Recalled by PD-Rx Pharmaceuticals, Inc. Due to CGMP...

The Issue: CGMP deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2023· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Simvastatin USP 40 mg Recalled by PD-Rx Pharmaceuticals, Inc. Due to CGMP...

The Issue: CGMP deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2023· Pharma Nobis LLC

Recalled Item: Fast Acting Earwax Removal System (carbamide peroxide) Recalled by Pharma...

The Issue: CGMP Deviations: active ingredient may be subpotent before the labeled...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 6, 2023· Karl Storz Endoscopy

Recalled Item: Metal Tray Recalled by Karl Storz Endoscopy Due to Metal sterilization trays...

The Issue: Metal sterilization trays used to encase and protect medical devices during...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· Elekta, Inc.

Recalled Item: Elekta Unity Image-Guided Radiation Therapy System containing an MR gradient...

The Issue: There is a low possibility that an electrical connector in the MR gradient...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· 3M Company - Health Care Business

Recalled Item: 3M Attest Steam Chemical Integrators Recalled by 3M Company - Health Care...

The Issue: 3M Attest Steam Chemical Integrators with dates of manufacture between...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· Fisher Wallace Laboratories Inc.

Recalled Item: Fisher Wallace Stimulator Models FW-100 and FW-200 Recalled by Fisher...

The Issue: If the batteries are installed incorrectly, the product may overheat,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· Hiossen Inc.

Recalled Item: ET III Nano-HA fixture System ET NH Dental Implant Model Recalled by Hiossen...

The Issue: Mis-labeled length of the dental implant on the Recall Implant's package....

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2023· 3M Company - Health Care Business

Recalled Item: 3M Attest Steam Chemical Integrators Recalled by 3M Company - Health Care...

The Issue: 3M Attest Steam Chemical Integrators with dates of manufacture between...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES (Med ES Main) Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to an automated dispensing cabinet software issue, when a medication...

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

Class II — Potential Health HazardOngoing