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. 2,598 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,598 in last 12 months

Showing 1276112780 of 49,990 recalls

DrugMarch 15, 2022· Teligent Pharma, Inc.

Recalled Item: Fluocinonide Topical Solution USP Recalled by Teligent Pharma, Inc. Due to...

The Issue: cGMP deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 15, 2022· Teligent Pharma, Inc.

Recalled Item: Econazole Nitrate Cream Recalled by Teligent Pharma, Inc. Due to cGMP...

The Issue: cGMP deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 15, 2022· Teligent Pharma, Inc.

Recalled Item: Gentamicin Sulfate Cream USP Recalled by Teligent Pharma, Inc. Due to cGMP...

The Issue: cGMP deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 15, 2022· Baxter Healthcare Corporation

Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...

The Issue: This correction is due to software anomalies occurring during use. If the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Baxter Healthcare Corporation

Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...

The Issue: This correction is due to software anomalies occurring during use. If the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Baxter Healthcare Corporation

Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...

The Issue: This correction is due to software anomalies occurring during use. If the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: TETRACAINE 1% Tetracaine HCI Injection Recalled by Vitae Enim Vitae...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: PHENOBARBITAL Sodium Injection Recalled by Vitae Enim Vitae Scientific, Inc....

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: PHENOBARBITAL Sodium Injection Recalled by Vitae Enim Vitae Scientific, Inc....

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: PAPAVERINE HYDROCHLORIDE Injection Recalled by Vitae Enim Vitae Scientific,...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Phenylephrine HCl Injection 50 mg per 250 mL in 0.9% Sodium Chloride...

The Issue: Defective container

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Epinephrine Injection 8 mg per 250 mL in 0.9% Sodium Chloride Recalled by...

The Issue: Defective container

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Norepinephrine Bitartrate Injection 8 mg per 250 mL in 0.9% Sodium Chloride...

The Issue: Defective container

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Norepinephrine Bitartrate Injection 16 mg per 250 mL added to Recalled by...

The Issue: Defective container

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

Class II — Potential Health HazardOngoing
Refund