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. 975 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
975 in last 12 months

Showing 34541–34560 of 49,990 recalls

DrugMarch 9, 2016· Teva Pharmaceuticals USA

Recalled Item: Amikacin Sulfate injection USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Presence of Particulate Matter: particulate matter identified as glass in...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 9, 2016· Whole Foods Market

Recalled Item: 365 Everyday Value Mango Frozen Fruit Bars 4 Bars-4 fl. Recalled by Whole...

The Issue: Undeclared coconut

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· Hill-Rom, Inc.

Recalled Item: Liko Universal SlingBars Universal SlingBar" 350 Recalled by Hill-Rom, Inc....

The Issue: The center bolt of the sling bar, which connects the bar to the patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· Pelton & Crane / Marus / DCI Equipment / KaVo

Recalled Item: Helios HL3T and HLT Track Mounted Dental Lights Product Usage: Recalled by...

The Issue: The firm received two customer complaints local Pelton & Crane distributors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Dextrose Injection Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Aminosyn-PF (amino acids) 7% Recalled by Hospira Inc. Due to Chemical...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Dextrose Injection Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Potassium Chloride Injection 20 mEq Recalled by Hospira Inc. Due to Chemical...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Dextrose Injection Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Mannitol I.V. Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2016· Integra LifeSciences Corp.

Recalled Item: Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments...

The Issue: Reports relating to unintended patient or operator burns or operator...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Estradiol III Recalled by Roche Diagnostics Operations, Inc. Due to Due to...

The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2016· Integra LifeSciences Corp.

Recalled Item: Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments...

The Issue: Reports relating to unintended patient or operator burns or operator...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2016· MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK

Recalled Item: VERO MHI-TM2000 Linear Accelerator System --- Common Name: Medical Linear...

The Issue: In rare cases the VERO/MHI-TM2000 Operator Console could set an incorrect...

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

Class II — Potential Health HazardOngoing