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. 2,455 recalls have been distributed to Indiana in the last 12 months.
Showing 53501–53520 of 53,528 recalls
Recalled Item: popchips¿ Sea Salt & Vinegar Recalled by Sonora Mills Foods Due to The firm...
The Issue: The firm received ingredient lactic acid from Kerry Ingredients and Flavors...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cheddar Mini Rice Snacks under the following brand names: Fred Meyer...
The Issue: The firm received ingredient lactic acid from Kerry Ingredients and Flavors...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: popchips¿ Cheddar Potato Recalled by Sonora Mills Foods Due to The firm...
The Issue: The firm received ingredient lactic acid from Kerry Ingredients and Flavors...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TSX-301A/2 Aquilion One CT System. The TSX-30IAl2 is a whole Recalled by...
The Issue: The SureStart function may not operate in the usual manner, and you may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXCELART Vantage Recalled by Toshiba American Medical Systems Inc Due to The...
The Issue: The status display in the sequence queue window may not change from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Impactor - Dorado IBC Recalled by SpineFrontier, Inc. Due to During...
The Issue: During two separate occasions an impactor plate on the handle broke off...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To...
The Issue: The outer jacket is receding away from the black sensor prematurely.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI PET/CT System Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: The reason for this inspection is to determine if the Spindle Block Servo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PT Link Waterbath Recalled by Dako North America Inc. Due to Dako is...
The Issue: Dako is recalling the PT Link Waterbath because of a possible electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba CT systems Recalled by Toshiba American Medical Systems Inc Due to...
The Issue: The systems all have a similar table control board. It has been found that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wildcat Creek Farms Country Style Butter Flavored Popcorn Salt Recalled by...
The Issue: Possible undeclared allergens. Milk, eggs, yellow #5, yellow #6 and red 40.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics...
The Issue: The power to the Esprit Display's Backlight is interrupted, causing the GUI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HiRes 90K devices with Helix Electrodes Model CI 1400-02H The Recalled by...
The Issue: Advanced Bionics is recalling the the HiRes 90K cochlear implant with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leflunomide tablets Recalled by Apotex Corp. Due to Subpotent (Single...
The Issue: Subpotent (Single Ingredient Drug): Distribution of product that did not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leflunomide tablets Recalled by Apotex Corp. Due to Subpotent (Single...
The Issue: Subpotent (Single Ingredient Drug): Distribution of product that did not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Radiological Image Processing System The system is an aid to Recalled by GE...
The Issue: The FluoroTrak Spinal Navigation Application on the OEC 9900 EliteNAV could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC MiniView 6800 Mobile Recalled by GE OEC Medical Systems, Inc Due to...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroView 2800 Recalled by GE OEC Medical Systems, Inc Due to Please be aware...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800 Plus Digital Recalled by GE OEC Medical Systems, Inc Due to Please...
The Issue: Please be aware that this is not a new recall. The firm has taken action;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cannulaide Recalled by Beevers Manufacturing & Supply, Inc. Due to...
The Issue: Cannulaide model CA 101 was recalled because the firm discovered this model...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.