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. 2,697 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,697 in last 12 months

Showing 1230112320 of 53,528 recalls

DrugJune 9, 2022· Green Pharmaceuticals, Inc.

Recalled Item: SnoreStop NasoSpray Recalled by Green Pharmaceuticals, Inc. Due to Microbial...

The Issue: Microbial contamination of non-sterile product: FDA laboratory analysis...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 9, 2022· Mayne Pharma Inc

Recalled Item: Clonidine Transdermal System Recalled by Mayne Pharma Inc Due to Defective...

The Issue: Defective Delivery System: Out of specification for release liner removal...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 9, 2022· Tomoorona LLC

Recalled Item: Qassim Mix for Coffee Recalled by Tomoorona LLC Due to The product is...

The Issue: The product is labeled to contain sodium caseinate, a milk derivative, but...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 9, 2022· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for falsely...

The Issue: There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott Laboratories

Recalled Item: Hemoglobin A1c for use with Architect Recalled by Abbott Laboratories Due to...

The Issue: There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for falsely...

The Issue: There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Randox Laboratories Ltd.

Recalled Item: Soluble Transferrin Receptors (STFR) Recalled by Randox Laboratories Ltd....

The Issue: A customer reported a problem with the reagent and calibrator. Randox...

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

Class III — Low RiskOngoing
Medical DeviceJune 9, 2022· Randox Laboratories Ltd.

Recalled Item: Soluble Transferrin Receptors Calibrator Series (STFR CAL) Recalled by...

The Issue: A customer reported a problem with the reagent and calibrator. Randox...

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

Class III — Low RiskOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolMax ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolFit ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCurve ZELTIQ Vaccum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCurve+ ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCore ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott

Recalled Item: Abbott TactiCath Sensor Enabled Recalled by Abbott Due to When connected to...

The Issue: When connected to the EnSite Precision Navigation System, an affected...

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

Class II — Potential Health HazardOngoing
FoodJune 8, 2022· Wilbur's Of Maine Chocolate Confections

Recalled Item: Wilbur's of Maine Milk Chocolate Covered Blueberries Recalled by Wilbur's Of...

The Issue: Product contains undeclared almonds.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 8, 2022· BUILT BRANDS LLC

Recalled Item: Built Bar Recalled by BUILT BRANDS LLC Due to Potential E. coli Contamination

The Issue: Banana Cream Pie Puff Protein Bars have the potential to be contaminated...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome HSI Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Precision Chronic Catheter Recalled by Covidien Llc Due to There...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Precision HSI Chronic Catheter Recalled by Covidien Llc Due to...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome H Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing