Recalls distributed in Indiana
These notices name Indiana in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
4,253 stored notices name Indiana, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Jul 14, 2021
Beech-Nut brand Single Grain Rice Baby Cereal; NET WT. 8 OZ (227g); INGREDIENTS: Rice flour, sunflower lecithin;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beechnut Nutrition
FDA (openFDA food enforcement)
Reported Jul 14, 2021
FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Heart Valves Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems, Kappa Freie Leichtkette (Human) kit for Roche cobas…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit, REF: PXVJ356, Pressure Monitoring Set, RX Only, CE, Sterile EO,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and PET/CT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Lyra SARS-CoV-2 Assay (M120) in vitro diagnostic test reagent
High riskUsing this product could cause serious injury, illness or death — stop using it now.Quidel Corporation
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Synaptive Trackable Suction Set Standard and Malleable
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synaptive Medical Inc.
FDA (openFDA device enforcement)
Reported Jun 30, 2021
Econocare Plus Waffle Overlay- Intended for use as a medical device to aid in the prevention and treatment of pressure…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.EHOB, Inc.
FDA (openFDA device enforcement)
Reported Jun 30, 2021
inLight Medical LED Pads used with Polychromatic light technology system
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Inlightened Partners LLC
FDA (openFDA device enforcement)
Reported Jun 30, 2021
reSET Mobile App, iOS and Android, provides cognitive behavioral therapy, as part of substance abuse treatment.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pear Therapeutics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 23, 2021
The Better-Bladder (BB), part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass circuits. Model: BB14
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Circulatory Technology Inc.
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Medtronic HY10Z48R2, Ctr., Custom Pack HY10Z48R2 Adult ECC 1/4, Custom Perfusion System, Sterile, Rx.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
24 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 23, 2021
BulkFoods.com brand dehydrated chopped celery in 1lb and 5lb plastic bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Natural Foods Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 23, 2021
Olde Thompson Organic Ground Coriander 1.5oz. in glass jar with flip-top lid. Sun Harvest Organic Coriander 1.5oz in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olde Thompson, LLC
FDA (openFDA food enforcement)
Reported Jun 23, 2021
OSSUR MIAMI J SELECT COLLAR - Product Usage: is intended to provide gross immobilization to the cervical spine. REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Atec Insignia Anterior Cervical Plate System, REF 136-0116, Insignia, ACP, 1-Level, 16 mm, Rx Only, Non-Sterile, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
28 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
ExacTrac Dynamic software, Model 20910-01B ETD Positioning and Monitoring Installer 1.0.2 - Product Usage: intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Jun 16, 2021
DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer semi-constrained cemented prosthesis. Part Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Jun 16, 2021
COVID-19 Self-Test Kit *** INNOVA *** 7T
High riskUsing this product could cause serious injury, illness or death — stop using it now.Innova Medical Group, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Normand Remisol Advance Data Manager is a software device that interfaces between laboratory information systems (LIS)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Normand-Info S.A.S.U.
FDA (openFDA device enforcement)
Reported Jun 16, 2021
WishBone Medical Plate and Screw System - Screw, Fixation, Bone, Washer, Bolt Nut. Part Number: PK-SMC0635NL-TI-US,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wishbone Medical, Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Indiana recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.