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. 2,697 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,697 in last 12 months

Showing 1236112380 of 53,528 recalls

DrugJune 3, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Tablet/Capsule Specification; oversized tablet found in a bottle

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 3, 2022· Prairie City Bakery

Recalled Item: Prairie City Bakery Peanut Butter Chocolate Chip Ooey Gooey Butter Recalled...

The Issue: Salmonella. Product contains recalled Jif peanut butter as ingredient.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 3, 2022· Abbott Laboratories

Recalled Item: Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Peach Mango...

The Issue: These products are being recalled due to the potential of leakage from the...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 3, 2022· Abbott Laboratories

Recalled Item: Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Raspberry...

The Issue: These products are being recalled due to the potential of leakage from the...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 3, 2022· Abbott Laboratories

Recalled Item: Pedialyte***Replaces Electrolytes***Great for Kids and Adults***Strawberry...

The Issue: The third party contract manufacturer used a dextrose ingredient derived...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 3, 2022· Ambu Inc.

Recalled Item: Ambu VivaSight 2 DLT Recalled by Ambu Inc. Due to Firm has received...

The Issue: Firm has received complaints on the device concerning leak/rupture of either...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2022· Stryker Neurovascular

Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...

The Issue: Microcatheter product label on the carton is missing the microcatheter...

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

Class II — Potential Health HazardOngoing
FoodJune 2, 2022· Wilton Industries Inc

Recalled Item: Wilton Rainbow Sprinkles Mix net wt 5.92 oz. item number 710-0-0627 Recalled...

The Issue: Milk contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 2, 2022· Wilton Industries Inc

Recalled Item: Wilton Rainbow Chip Crunch Sprinkles net wt 5.25 oz. item 710-5364 Recalled...

The Issue: Milk contamination

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 2, 2022· GE Healthcare, LLC

Recalled Item: Service manuals for the CT Recalled by GE Healthcare, LLC Due to As a result...

The Issue: As a result of unclear guidance in the service manual, the table can drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2022· Surgical Innovations Ltd

Recalled Item: YelloPort Elite Universal Seal. For use in laparoscopic procedures. Recalled...

The Issue: There is the potential that YelloPort Elite Universal Seals packaging may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2022· Breas Medical, Inc.

Recalled Item: Vivo 45LS Ventilator- intended to provide continuous or intermittent...

The Issue: A forced shutdown of one of the processors did not generate a watch dog...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2022· Wright Medical Technology, Inc.

Recalled Item: Stryker INFINITY Resect Guide for INBONE Talus Recalled by Wright Medical...

The Issue: The instrument is incorrectly color coded.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2022· CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD.

Recalled Item: DVR Anatomic Recalled by CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD. Due to...

The Issue: One lot of DVRASL plates were incorrectly etched and may have been placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2022· Skytron, Div. The KMW Group, Inc

Recalled Item: Product Name: GCX Channel Mounting Accessory Model/Catalog Number:...

The Issue: Under certain circumstances, the mounting screws may loosen or pull out from...

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

Class II — Potential Health HazardOngoing
FoodJune 1, 2022· Taylor Farms Retail Inc

Recalled Item: Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk...

The Issue: Undeclared allergen (peanuts) from incorrect master pack. Salad kit contains...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 1, 2022· GE Healthcare, LLC

Recalled Item: GE Healthcare Aisys CS2 Anesthesia System Recalled by GE Healthcare, LLC Due...

The Issue: There is a potential reversal of the O2 and air cylinder pressure transducer...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2022· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9B SP1. For radiation treatment planning. Recalled by RAYSEARCH...

The Issue: An issue with propagation of treatment course information from RayStation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Ventana Medical Systems Inc

Recalled Item: Ventana HE 600 System Recalled by Ventana Medical Systems Inc Due to There...

The Issue: There is a potential for fluid leak inside the Ventana HE 600 instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Spectranetics Corporation

Recalled Item: Philips Laser System Recalled by Spectranetics Corporation Due to The...

The Issue: The LAS-100 Laser system may detect an inoperable hardware component during...

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

Class II — Potential Health HazardOngoing