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. 2,617 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,617 in last 12 months

Showing 1090110920 of 49,990 recalls

DrugOctober 4, 2022· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...

The Issue: Defective Container: Complaints received of vial breakage and glass flying...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 4, 2022· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...

The Issue: Defective Container: Complaints received of vial breakage and glass flying...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 3, 2022· Beckman Coulter, Inc.

Recalled Item: MicroScan autoSCAN-4 Instrument Recalled by Beckman Coulter, Inc. Due to Due...

The Issue: Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat. No. 662995)...

The Issue: Due to partial label detachment on tubes. This can cause tubes to become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Trucount Tubes (Cat. No. 663028) Recalled by Becton, Dickinson and...

The Issue: Due to partial label detachment on tubes. This can cause tubes to become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Rebiscan, Inc.

Recalled Item: Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for...

The Issue: Unable to charge the battery pack- battery packs will allow the batteries to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Trucount Tubes (Cat. No. 340334) Recalled by Becton, Dickinson and...

The Issue: Due to partial label detachment on tubes. This can cause tubes to become...

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

Class II — Potential Health HazardOngoing
DrugSeptember 30, 2022· AuroMedics Pharma LLC

Recalled Item: Fondaparinux Sodium Injection Recalled by AuroMedics Pharma LLC Due to...

The Issue: Subpotent Drug: Out of specification for assay

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2022· VistaPharm, Inc.

Recalled Item: Pyridostigmine Bromide Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: cGMP Deviations: Out of specification for assay of one of the preservative...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2022· Ingenus Pharmaceuticals Llc

Recalled Item: Flunisolide Nasal Solution Recalled by Ingenus Pharmaceuticals Llc Due to...

The Issue: Out of specification for related substances (impurities).

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 30, 2022· Boston Scientific Corporation

Recalled Item: EMBLEM MRI S-ICD Recalled by Boston Scientific Corporation Due to There is...

The Issue: There is an incorrect manufacturing date/timestamp within the software which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE DENTAL PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O Recalled by...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· Boston Scientific Corporation

Recalled Item: EMBLEM S-ICD Recalled by Boston Scientific Corporation Due to There is an...

The Issue: There is an incorrect manufacturing date/timestamp within the software which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CVC BARRIER KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE RADIOLOGY PROCEDURE PACK Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB BASIC OPHTHALMIC PACK Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB CATARACT TRAY Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE LITHOTOMY Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB PHACO PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing