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 3742137440 of 53,528 recalls

Medical DeviceDecember 9, 2015· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...

The Issue: Incorrect drug dosage due to "Age Limit" and patient weight data item issue.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...

The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer WIZARD2 2-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2015· Perkinelmer

Recalled Item: Perkin Elmer ClWIZARD2 5-detector Recalled by Perkinelmer Due to The content...

The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...

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

Class II — Potential Health HazardOngoing
DrugDecember 7, 2015· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP 5 mg Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; Impurity A

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

Class III — Low RiskOngoing
Refund
FoodDecember 7, 2015· C. H. Guenther & Son, Inc.dba Morrison Milling

Recalled Item: Pioneer Sweet Corn Muffin Mix NET WT. 5 LBS 2.27 kg Recalled by C. H....

The Issue: May contain small metal fragments from wire mesh sifter.

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

Class III — Low RiskOngoing
Refund
FoodDecember 7, 2015· C. H. Guenther & Son, Inc.dba Morrison Milling

Recalled Item: HSRG Cornmeal Breader NET WT 25 LB (11.33 kg) Recalled by C. H. Guenther &...

The Issue: May contain small metal fragments from wire mesh sifter.

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

Class III — Low RiskOngoing
Refund
FoodDecember 7, 2015· C. H. Guenther & Son, Inc.dba Morrison Milling

Recalled Item: Morrison's Pancake Mix Net Wt 5 LB (2.27 kg) Recalled by C. H. Guenther &...

The Issue: May contain small metal fragments from wire mesh sifter.

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

Class III — Low RiskOngoing
Refund
FoodDecember 7, 2015· C. H. Guenther & Son, Inc.dba Morrison Milling

Recalled Item: HEB Lemon Seasonal Fish Fry Mix NET WT. 16 OZ Recalled by C. H. Guenther &...

The Issue: May contain small metal fragments from wire mesh sifter.

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

Class III — Low RiskOngoing
Refund
FoodDecember 7, 2015· C. H. Guenther & Son, Inc.dba Morrison Milling

Recalled Item: Buttermilk Pancake Mix # 1 NET WT 5 LBS (2.27kg) Recalled by C. H. Guenther...

The Issue: May contain small metal fragments from wire mesh sifter.

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

Class III — Low RiskOngoing
Refund
FoodDecember 7, 2015· C. H. Guenther & Son, Inc.dba Morrison Milling

Recalled Item: HEB Cheddar Bacon Flavored Cornbread Mix NET WT. 13.3 OZ Recalled by C. H....

The Issue: May contain small metal fragments from wire mesh sifter.

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

Class III — Low RiskOngoing
Refund