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 2682126840 of 53,528 recalls

Medical DeviceJune 27, 2018· Elekta Instrument AB

Recalled Item: Leksell GammaPlan 11.1 Product Usage: Leksell GammaPlan is a computer-based...

The Issue: The margin tool in Leksell GammaPlan 11.1 systematically overestimates...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Gantry rotation or...

The Issue: Gantry rotation or proton irradiation can be allowed even if apertures or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Single Detector (Stitching Patient Support) 712020 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Recalled by Philips Medical Systems Gmbh, DMC Due to The...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Out-of-specification results for the Enalapril Diketopiperazine degradation...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2018· Genicon, Inc.

Recalled Item: Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: Recalled by...

The Issue: Genicon is providing updated IFU labeling to users to provide clarity on how...

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

Class II — Potential Health HazardOngoing
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Red Maeng Da Recalled by World Organix, LLC Due to...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Kratom+CBD CBD infused Maeng Da Recalled by World Organix,...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Gold Series Ultra Enhanced Indo Recalled by World Organix,...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Recalled by World Organix, LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· MAJOR PHARMACEUTICALS

Recalled Item: Enalapril Maleate Tablets Recalled by MAJOR PHARMACEUTICALS Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Sub-recall because this...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2018· MAJOR PHARMACEUTICALS

Recalled Item: Enalapril Maleate Tablets Recalled by MAJOR PHARMACEUTICALS Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Sub-recall because this...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 26, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood parameter monitoring system 500 H/SAT Recalled by Terumo...

The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2018· Encore Medical, Lp

Recalled Item: Instrument trays used to store AltiVate Small Shell Trials (FA Recalled by...

The Issue: A black, aluminum oxide coating may appear on the tray after cleaning. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Monitor with one Blood Parameter Module and one HSat Probe Recalled by...

The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...

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

Class II — Potential Health HazardOngoing