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. 2,507 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,507 in last 12 months

Showing 3716137180 of 53,528 recalls

Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Radial Artery Pressure Monitoring Catheter Sets and Trays The subject...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Single Lumen Central Venous Catheter Sets and Trays The subject Recalled by...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Femoral Artery Pressure Monitoring Catheter Sets and Trays The subject...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Single Lumen Pressure Monitoring Sets and Trays The subject sets Recalled by...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Synthes (USA) Products LLC

Recalled Item: Cervical Spine Locking Plate (CSLP) System Recalled by Synthes (USA)...

The Issue: DePuy Synthes is initiating a Voluntary Medical Device Recall of lot #...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

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

Class II — Potential Health HazardOngoing
FoodJanuary 6, 2016· Bearded Brothers LLC

Recalled Item: Bearded Brothers BOLD Coconut Curry Net Wt. 1.5 oz/43 g . Recalled by...

The Issue: Mold on energy bars.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 6, 2016· Bearded Brothers LLC

Recalled Item: Bearded Brothers BOLD The Greek Net Wt. 1.5 oz/43 g . Recalled by Bearded...

The Issue: Mold on energy bars.

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

Class II — Potential Health HazardOngoing
Refund