Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,507 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,507 in last 12 months

Showing 3648136500 of 53,528 recalls

Medical DeviceMarch 9, 2016· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient...

The Issue: Panorama Central Station including the work station View Station, View...

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

Class II — Potential Health HazardOngoing
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
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
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: 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: 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
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· 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· 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
FoodMarch 8, 2016· Welle Pty Ltd

Recalled Item: The Super Elixir By WelleCo Australia Alkalising Greens 150g/5.3 oz net...

The Issue: Welle Pty Ltd is recalling Wellco Super Elixir pouches because of potential...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 7, 2016· Prayon Inc.

Recalled Item: Phosphoric Acid Recalled by Prayon Inc. Due to Potential contamination with...

The Issue: Potential contamination with trace levels of 1-methylethyl benze (more...

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

Class III — Low RiskOngoing
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 II Elecsys and cobas e analyzers 190 Recalled by Roche Diagnostics...

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