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. 2,544 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,544 in last 12 months

Showing 3060130620 of 53,528 recalls

Medical DeviceJune 5, 2017· Angiodynamics, Inc.

Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...

The Issue: The firm is recalling product that has the potential to not function during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: COMP PRIMARY STEM 8MM MINI Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Angiodynamics, Inc.

Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...

The Issue: The firm is recalling product that has the potential to not function during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: Lateral Troch Plate Full Crimp - 254mm Recalled by Zimmer Biomet, Inc. Due...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Zimmer Biomet, Inc.

Recalled Item: CER BIOLOXD OPTION HD 32MM Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Possibility that the patient label inside the product box was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2017· Angiodynamics, Inc.

Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...

The Issue: The firm is recalling product that has the potential to not function during...

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

Class II — Potential Health HazardOngoing
DrugJune 5, 2017· Bristol-myers Squibb Company

Recalled Item: EliquisTablets 5mg Recalled by Bristol-myers Squibb Company Due to Labeling:...

The Issue: Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 5, 2017· Apothecary By Design

Recalled Item: Progesterone Injection in Olive Oil With Benzyl Alcohol 10% Recalled by...

The Issue: Lack of Processing Controls: The metal container closure adheres to the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2017· G & W Laboratories, Inc.

Recalled Item: G & W Clobetasol Propionate Ointment 0.05% Recalled by G & W Laboratories,...

The Issue: Failed impurities/degradation specifications: This product is being recalled...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim 5 Elite Recalled by St. Jude Medical, Inc. Due to The firm...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· C.R. Bard, Inc.

Recalled Item: BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension Recalled...

The Issue: Customer complaint of a cut in the side of the leg bag, indicating a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim 7 Elite Recalled by St. Jude Medical, Inc. Due to The firm...

The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2017· Sterilmed Inc

Recalled Item: St. Jude Medical. Agilis NxT Steerable Introducer: B1-Directional Recalled...

The Issue: Inadequate seal due to lack of adhesive glue

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

Class I — Serious Health HazardOngoing
FoodJune 2, 2017· Star Snacks Co., Llc.

Recalled Item: Southern Grove Cashew Halves & Pieces with Sea Salt Recalled by Star Snacks...

The Issue: The firm received notification from a consumer finding a glass fragment in...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2017· Schnucks Markets Corporate Office

Recalled Item: Schnucks Bakery Recalled by Schnucks Markets Corporate Office Due to The...

The Issue: The scale label generated for cake slices at the store level fails to...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 1, 2017· Schnucks Markets Corporate Office

Recalled Item: 1) Schnucks Bakery Recalled by Schnucks Markets Corporate Office Due to The...

The Issue: The scale label generated for cake slices at the store level fails to...

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

Class I — Serious Health HazardOngoing
Refund