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. 2,725 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,725 in last 12 months

Showing 1020110220 of 53,528 recalls

DrugFebruary 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Norepinephrine Bitartrate in 0.9% Sodium Chloride Injection Recalled by...

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
DrugFebruary 22, 2023· Nephron Sterile Compounding Center LLC

Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...

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
DrugFebruary 21, 2023· Padagis US LLC

Recalled Item: Evamist (estradiol transdermal spray) Recalled by Padagis US LLC Due to...

The Issue: Failed Content Uniformity Specifications: The Spray Content Uniformity (SCU)...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 40 mg (160 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 0.5 mg per 5 mL (100 mcg/mL) Recalled by Denver Solutions,...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 1mg per 10mL (100 mcg/mL) 10 mL syringes Recalled by...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 21, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Phenylephrine HCl 20 mg (80 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV...

The Issue: CGMP DEVIATIONS

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 21, 2023· Chukar Cherry Company Inc.

Recalled Item: Chukar Cherries Cherry Bombs Bits 'n Pieces Recalled by Chukar Cherry...

The Issue: undeclared hazelnuts

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 21, 2023· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...

The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...

The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Biosense Webster, Inc.

Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...

The Issue: Incorrect labeling; specifically, the product name, lot number and product...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Biosense Webster, Inc.

Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...

The Issue: Incorrect labeling; specifically, the product name, lot number and product...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Lysis Beads Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Preat Corp

Recalled Item: Neodent GM X 6mm Engaging Titanium Base Recalled by Preat Corp Due to...

The Issue: Engaging titanium base contains a dimensional condition that allows vertical...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Reagent RVD with RVD Enhancer: a) 1 mL Recalled by Entopsis , Inc....

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis BCSNano (1mL) Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Support: a) 1 mL Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Reagent RVD-RT Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Activator: a) 1.5mL Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Reagent Buccal Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing