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. 2,547 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,547 in last 12 months

Showing 2542125440 of 53,528 recalls

Medical DeviceSeptember 4, 2018· CooperSurgical, Inc.

Recalled Item: Colpo-Pneumo Occluder Recalled by CooperSurgical, Inc. Due to The seal of...

The Issue: The seal of the sterile pouch may be compromised, thereby increasing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· GE Healthcare Finland Oy

Recalled Item: GE Healthcare CARESCAPE Monitor B450 Product Usage: Intended uses of...

The Issue: When multiple CARESCAPEMonitor B450 or B850 units are connected to the same...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· CooperSurgical, Inc.

Recalled Item: Retractor System Elastic Stays (Part 3314-lG Recalled by CooperSurgical,...

The Issue: There is a possibility that the seal of the sterile pouch may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Hemotherm 400CE Recalled by Cincinnati Sub-Zero Products LLC, a Gentherm...

The Issue: Potential for membrane (control panel) switch errors leading to an inability...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Vereos PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Software Correction: Software errors that may result in incorrect 4D CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· GE Healthcare Finland Oy

Recalled Item: GE Healthcare CARESCAPE Monitor B850 Product Usage: Intended uses of...

The Issue: When multiple CARESCAPEMonitor B450 or B850 units are connected to the same...

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

Class II — Potential Health HazardOngoing
DrugSeptember 4, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Tizanidine HCl Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Presence of Foreign Tablets/Capsules: Glimepiride tablet was found in a...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2018· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Synjardy (empagliflozin and metformin hydrochloride) Tablets. 5 mg/1000 mg....

The Issue: Cross Contamination With Other Products:

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Colds & Flu Response Homeopathic Formula Recalled by Beaumont Bio-med, Inc....

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Sinus Response Homeopathic Formula Recalled by Beaumont Bio-med, Inc. Due to...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Muscle & Joint Pain Relief Homeopathic Formula Recalled by Beaumont Bio-med,...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Sore Throat & Laryngitis Response Homeopathic Formula Recalled by Beaumont...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Skin Irritation & Itch Response Homeopathic Formula Recalled by Beaumont...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Allergy & Hay Fever Relief Homeopathic Formula Recalled by Beaumont Bio-med,...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· BioLyte Laboratories, LLC

Recalled Item: NeoRelief for Muscle Cramping & Restlessness Homeopathic Topical Gel...

The Issue: CGMP Deviations: finished product produced with active ingredients recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Diarrhea Response Homeopathic Formula Recalled by Beaumont Bio-med, Inc. Due...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Arthritis Pain Relief Homeopathic Formula Recalled by Beaumont Bio-med, Inc....

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 31, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: VirtuoSaph Plus Endoscopic Vessel Harvesting System Recalled by Terumo...

The Issue: The system's IFU contains a list of generators that the have been deemed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2018· GE Healthcare, LLC

Recalled Item: Dash 4000 Patient Monitoring System is used to monitor physiologic Recalled...

The Issue: The patient monitors may simultaneously restart as designed if all are...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2018· GE Healthcare, LLC

Recalled Item: Dash 5000 Patient Monitoring System is used to monitor physiologic Recalled...

The Issue: The patient monitors may simultaneously restart as designed if all are...

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

Class II — Potential Health HazardOngoing