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. 2,768 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,768 in last 12 months

Showing 24212440 of 53,528 recalls

DrugMay 21, 2025· Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado)

Recalled Item: Semaglutide/Cyanocobalamin Injectable Recalled by Thrive Health and...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2025· Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado)

Recalled Item: Tirzepatide Injections Recalled by Thrive Health and Wellness, LLC, dba...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2025· Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado)

Recalled Item: Nicotinamide adenine dinucleotide (NAD+): 100mg/mL Recalled by Thrive Health...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2025· Umary-USA.com

Recalled Item: UNAVY ACIDO HIALURONICO Recalled by Umary-USA.com Due to Undeclared Ingredients

The Issue: Marketed without approved NDA/ANDA- Laboratory analysis found product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 21, 2025· Umary-USA.com

Recalled Item: UMOVY ACIDO HIALURONICO Recalled by Umary-USA.com Due to Undeclared Ingredients

The Issue: Marketed without approved NDA/ANDA- Laboratory analysis found product to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: BD Insyte Autoguard Winged Shielded IV Catheter Recalled by Becton Dickinson...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· BIGFOOT BIOMEDICAL

Recalled Item: Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen...

The Issue: Due to a software/firmware issue diabetes management system may provide a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Jolife AB

Recalled Item: LUCAS 2 Recalled by Jolife AB Due to Due to demonstration units of chest...

The Issue: Due to demonstration units of chest compression system being provided to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Covidien

Recalled Item: Newport HT70 Ventilator Recalled by Covidien Due to Ventilator Printed...

The Issue: Ventilator Printed Circuit Board Assembly may have two separate capacitors...

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

Class I — Serious Health HazardOngoing
FoodMay 20, 2025· JFE FRANCHISING INC

Recalled Item: Yaki Noodle Bowl 12 oz 63912389254 Ebi Vermicelli Bowl 13oz Recalled by JFE...

The Issue: Cucumbers have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2025· JFE FRANCHISING INC

Recalled Item: Cucumber with Ranch - 9 oz 63912395020 Cucumber Recalled by JFE FRANCHISING...

The Issue: Cucumbers have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2025· JFE FRANCHISING INC

Recalled Item: Bibimbap Bowl 13 oz 63912389259 Recalled by JFE FRANCHISING INC Due to...

The Issue: Cucumbers have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund