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 2844128460 of 53,528 recalls

Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: CINtec PLUS Cytology Kit (CE-IVD) Recalled by Ventana Medical Systems Inc...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: OptiView Amplification Kit (250 Test) Recalled by Ventana Medical Systems...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: OptiView DAB IHC Detection Kit Recalled by Ventana Medical Systems Inc Due...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: ultraView SISH Detection Kit Recalled by Ventana Medical Systems Inc Due to...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

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

Class I — Serious Health HazardOngoing
DrugDecember 18, 2017· Osmotica Pharmaceutical Corp

Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugDecember 18, 2017· Osmotica Pharmaceutical Corp

Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
FoodDecember 18, 2017· Gel Spice Co, Inc.

Recalled Item: Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) Recalled by Gel...

The Issue: Gel Spice, Inc. is recalling three beef flavored bouillon cube products...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2017· Gel Spice Co, Inc.

Recalled Item: Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) Recalled by Gel...

The Issue: Gel Spice, Inc. is recalling three beef flavored bouillon cube products...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2017· Meijer Distribution, Inc

Recalled Item: Meijer Michigan Harvest Salad 10 Oz retail unit in plastic Recalled by...

The Issue: Sliced apples within the products being potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2017· Meijer Distribution, Inc

Recalled Item: Meijer Sharable Waldorf Salad 16 Oz retail unit in plastic Recalled by...

The Issue: Sliced apples within the products being potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2017· Meijer Distribution, Inc

Recalled Item: Meijer Fresh Cranberry Apple Stuffing Starter 18.9 Oz retail unit Recalled...

The Issue: Sliced apples within the products being potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 18, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G....

The Issue: Package integrity failure observed during routine shift package integrity...

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

Class II — Potential Health HazardOngoing