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. 2,462 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,462 in last 12 months

Showing 4332143340 of 53,528 recalls

Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM PERMANENT CAUTERY SPATULA Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Elekta, Inc.

Recalled Item: MOSAIQ Product Usage: MOSAIQ is an oncology information system used Recalled...

The Issue: A problem can exist in MOSAIQ resulting in the display of incorrect numeric...

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

Class II — Potential Health HazardOngoing
FoodOctober 31, 2014· Nature's Way Purewater Systems, Inc.

Recalled Item: ESSENTIA Hydration Perfected Purified Water and Electrolytes Recalled by...

The Issue: Product may contain mold.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2014· Accuray Incorporated

Recalled Item: CyberKnife Robotic Radiosurgery System with the first generation IRIS...

The Issue: Software upgrade to correct potential safety issue related to CyberKnife...

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

Class II — Potential Health HazardOngoing
DrugOctober 30, 2014· Baxter Healthcare Corp.

Recalled Item: Heparin Sodium in 0.9% Sodium Chloride Injection Recalled by Baxter...

The Issue: Subpotent Drug: Heparin raw material was found to have low potency

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 30, 2014· Alcon Research, Ltd.

Recalled Item: INFINITI VISION SYSTEM ULTRASOUND FMS. Single-use fluid management system....

The Issue: Alcon is conducting a medical device recall due to the possible presence of...

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

Class II — Potential Health HazardOngoing
FoodOctober 29, 2014· Mt. Olive Pickle Company Inc

Recalled Item: Mt. Olive Recalled by Mt. Olive Pickle Company Inc Due to Product may...

The Issue: Product may contain glass fragments.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 29, 2014· Radiometer America Inc

Recalled Item: Crea A and B membranes Recalled by Radiometer America Inc Due to Negative...

The Issue: Negative drift on QC during in-use lifetime of CREA membranes can be observed.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2014· Respironics California Inc

Recalled Item: Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit...

The Issue: If the power supply fan mounting screws are installed incorrectly, the ends...

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

Class II — Potential Health HazardOngoing
FoodOctober 28, 2014· Marathon Ventures Inc

Recalled Item: Macadamia nuts in various formats: (1.) Western Family Macadamia Diced Nuts...

The Issue: Macadamia nuts may have possible contamination with Salmonella florida.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 28, 2014· Cooper Vision Caribbean Corp.

Recalled Item: Soft Contact Lens Recalled by Cooper Vision Caribbean Corp. Due to Portions...

The Issue: Portions of the lots may contain units with an incorrect lens axis condition.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Inspiration system: Product Usage: mammography exams Recalled by...

The Issue: It was determined that if the Mammomat Inspiration system is not secured to...

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

Class II — Potential Health HazardOngoing
FoodOctober 27, 2014· Kent Precision Foods Group, Inc.

Recalled Item: Chicken flavored broth base and seasoning Recalled by Kent Precision Foods...

The Issue: Orrington Farms Chicken Flavored Broth Base & Seasoning, Low Sodium labels...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 27, 2014· Straumann USA, LLC

Recalled Item: Drill set long Recalled by Straumann USA, LLC Due to Drill set may contain...

The Issue: Drill set may contain incorrect drill.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2014· ArthroCare Medical Corporation

Recalled Item: Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger...

The Issue: Potential breach of sterile barrier due to defective product tray.

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

Class II — Potential Health HazardOngoing