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. 1,055 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,055 in last 12 months

Showing 19281–19300 of 53,528 recalls

DrugMay 22, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 90 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.

The Issue: Superpotent Drug.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2020· The Harvard Drug Group

Recalled Item: Doxycycline Hyclate Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Dissolution Specification: The dissolution test at the 24 month time...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 30 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.

The Issue: Superpotent Drug.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 22, 2020· Teva Pharmaceuticals USA

Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Some bottles may contain mixed strengths of the product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 21, 2020· Vitalconnect Inc.

Recalled Item: VistaSolution Recalled by Vitalconnect Inc. Due to A healthcare provider...

The Issue: A healthcare provider (HCP) noticed a patient had a lowered historic SpO2...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System - Software Versions 3.3.3 and Recalled by...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Software Versions 3.3.3 and below Product...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS XT 7600 Integrated System Software Versions 3.5.1 and below Recalled...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System - Product Code: 6802914 Unique Recalled...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System Software Versions 3.3.3 and below...

The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2020· Philips North America, LLC

Recalled Item: Philips SureSigns VM1SpO2 Recalled by Philips North America, LLC Due to...

The Issue: Philips has identified a Philips SureSigns VM1 monitor in the possession of...

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

Class II — Potential Health HazardOngoing
DrugMay 19, 2020· Flexion Therapeutics, Inc.

Recalled Item: Zilretta (triamcinolone acetonide extended-release injectable suspension)...

The Issue: Temperature Abuse: Product was stored at room temperature longer than 6...

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

Class III — Low RiskOngoing
Refund
DrugMay 19, 2020· Wuhan Bingbing Pharmaceutical Co., Ltd.

Recalled Item: Mencaine (lidocaine 4.5% Recalled by Wuhan Bingbing Pharmaceutical Co., Ltd....

The Issue: CGMP Deviations: due to the loss of product manufacturing records and retain...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 19, 2020· American Health Packaging

Recalled Item: Doxycycline Hyclate Tablets Recalled by American Health Packaging Due to...

The Issue: Failed dissolution specification - dissolution results of 59% (spec. NLT...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 19, 2020· Wuhan Bingbing Pharmaceutical Co., Ltd.

Recalled Item: LidoPatch (lidocaine HCl 3.6% Recalled by Wuhan Bingbing Pharmaceutical Co.,...

The Issue: CGMP Deviations: due to the loss of product manufacturing records and retain...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 19, 2020· Wuhan Bingbing Pharmaceutical Co., Ltd.

Recalled Item: Maximum Strength Lidocaine Cold & Hot Patch (lidocaine 4% Recalled by Wuhan...

The Issue: CGMP Deviations: due to the loss of product manufacturing records and retain...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 19, 2020· Wuhan Bingbing Pharmaceutical Co., Ltd.

Recalled Item: LidoPro (lidocaine 4% Recalled by Wuhan Bingbing Pharmaceutical Co., Ltd....

The Issue: CGMP Deviations: due to the loss of product manufacturing records and retain...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 7 Recalled by RAYSEARCH LABORATORIES AB Due to Software error was...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 6 Service Pack 2 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 8A Service Pack 1 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software error was identified in the Pencil Beam Scanning (PBS) and Line...

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

Class II — Potential Health HazardOngoing