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 48,122 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Mar 6, 2019
Draco Enzymatic Deep-Cleaning Pads, Product Number HY0305Z Product Usage: Multi-tiered enzymatic detergent contains…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Madison Polymeric Engineering
FDA (openFDA device enforcement)
Reported Mar 6, 2019
The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is intended to be used for radiologic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems USA Com
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle screw fixation is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet Spine Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2019
AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2019
Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Feb 20, 2019
COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chicago Bar Company LLC Rxbar
18 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
Hemotherm CE Dual Reservoir Cooler/Heater, Model No. 400CE Product Usage: The HEMOTHERM¿ Model 400CE Dual Reservoir…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products LLC, a Gentherm Company
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Culinary Secrets, Butterscotch Instant Pudding Mix, Net Wt. 28 OZ, Marketed by Independent Marketing Alliance, Houston,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Diamond Crystal Brands, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Organic Sunflower Butter, Net Wt. 16 oz. (453g) Packaged under the following brand names: 1. Thrive Market, UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oskri Corp.
19 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
Parent's Choice Toddler Next Stage¿ Milk Drink Powder Natural Milk Flavor With Other Natural Flavors, Stage 3, 1 Year…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PBM Nutritionals, LLC
FDA (openFDA food enforcement)
Reported Feb 13, 2019
ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 13, 2019
BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature Sensing Infection Control Foley Catheter with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Medical Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Gold Medal Unbleached All Purpose Flour. Net Wt 5 lb. (2.26kg). UPC 16000-19610. Distributed By General Mills Sales,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.General Mills, Inc.
FDA (openFDA food enforcement)
Reported Feb 13, 2019
Henry Schein CU 1000 Halogen Curing Light, Catalog 900-4542. - Product Usage: Curing light for use in dentistry. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Handpiece Headquarters
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
12 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Chicago's Pizza Base Mix, Manufactured Exclusively for Chicago's Pizza, Greenfield, IN packaged in 30 lb bags.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pizza Blends, LLC
9 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 13, 2019
Product: ABL800 FLEX with Crea. The ABL800 with Crea is available in the following configurations: ABL817, ABL827 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Feb 6, 2019
Cell Saver 5/5+ Bowl Set, 70ml, Product ID: 0291E-00, 0291A-00 Indications for Use: The Haemonetics Cell Saver 5/5+…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haemonetics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 6, 2019
Calix Lumbar Spinal Implant System: 22mm x 10mm x 7mm PLIF ASSY PC, REF X034-0172PC 22mm x 10mm x 8mm PLIF ASSY PC, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xtant Medical Inc.
FDA (openFDA device enforcement)
Reported Jan 30, 2019
Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seasoned with Red & Green Peppers. NET WT 15.25 oz. (432 g);…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Research Center - Walnut Creek
FDA (openFDA food enforcement)
Reported Jan 30, 2019
Perfusion Pack, Rx only, Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA
FDA (openFDA device enforcement)
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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.