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. 1,008 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,008 in last 12 months

Showing 37421–37440 of 53,528 recalls

DrugDecember 9, 2015· Lucy's Weight Loss (dba. Waisted With Lucy)

Recalled Item: Pink Bikini capsules Recalled by Lucy's Weight Loss (dba. Waisted With Lucy)...

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
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 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
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 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 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 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 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· 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 7, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM systems Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Possible installation error of the quench lines of superconducting magnets,...

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
Medical DeviceDecember 7, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Coil overheating...

The Issue: Coil overheating can occur when the device is used in Mode 2 setup. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue with the...

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

Class II — Potential Health HazardOngoing
FoodDecember 7, 2015· C. H. Guenther & Son, Inc.dba Morrison Milling

Recalled Item: Champs Chicken Batter Mix Net Wt. 25 lbs. (11.33 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: Krispy Krunchy Chicken Fish Fry Net Weight 5 Lbs. (2.27kg) 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: Hartz Krispy Chicken 'N' Rolls Milk Dip Net Wt 20 LBS (9.07 kg) Recalled by...

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