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.
Showing 27441–27460 of 53,528 recalls
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Stockert Heater-Cooler System 3T Recalled by LivaNova USA Due to Firm...
The Issue: Firm is notifying customers that the Deep-Cleaning Service is now available...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets USP Recalled by Sun Pharmaceutical...
The Issue: Presence of Foreign Substance:Sun Pharma is recalling one (1) lot of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimension Gentamicin Flex reagent cartridge Recalled by Siemens Healthcare...
The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Gentamicin Flex reagent cartridge Recalled by Siemens...
The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroAire SmartRelease Endoscopic System Recalled by MicroAire Surgical...
The Issue: The Instructions for Use (IFU) is incorrect with regards to sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLISTA StandOP (model 600) surgical lights shipped from October 2012...
The Issue: Potential keypad failure on VOLISTA StandOP Surgical Lights.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smoked Salmon Spread 5 lb. bulk units Recalled by Superior Foods Company Due...
The Issue: Superior Foods Company is voluntarily recalling a specific lot of Smoked...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Wheat Chocolate Animal Cookies Recalled by NatureBox, Inc. Due to...
The Issue: While packing from a bulk bin of whole wheat chocolate animal cookies, 2...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mitragyna Speciosa Leaf Powder-GREEN Horn Recalled by Viable Solutions, LLC...
The Issue: Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mitragyna Speciosa Leaf Powder-Thai Maeng Da Recalled by Viable Solutions,...
The Issue: Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa...
The Issue: Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only...
The Issue: Failed Dissolution Specification: Low dissolution outside of specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLAST Bandage Recalled by Tactical Medical Solutions, Inc. Due to Blast...
The Issue: Blast Bandages (part# BLAST) with Lot# 0617 were not terminally sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators Recalled by...
The Issue: There is a potential for the cord to spark and cause a fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Euphoric Premium Male Performance Enhancer capsules Recalled by Epic...
The Issue: Marketed Without An Approved NDA/ANDA: product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Southwestern Gourmet Butter Popcorn Grand Canyon Foods Recalled by Grand...
The Issue: An FDA inspection revealed products that contained Yellow 5 and soy lecithin...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southwestern Gourmet Prickly Pear Popcorn Grand Canyon Foods Recalled by...
The Issue: An FDA inspection revealed products that contained Yellow 5 and soy lecithin...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...
The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...
Recommended Action: Do not consume. Return to store for a refund or discard.