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 Aug 17, 2022
Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water beverage with other natural flavors; 1-liter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Refresco Beverages US Inc.
FDA (openFDA food enforcement)
Reported Aug 17, 2022
cobas e801 Immunoassay Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Xhibit Telemetry Receiver, Model: 96280
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2022
EkoSonic Kit 135cm, 12cm TZ The EkoSonic Endovascular Device is packaged as a kit that includes both the USC and IC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2022
The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
Dose Vital VIP Products Vital Honey With Caviar and Tongkat Ali Powder; 12 sachets-15g
High riskUsing this product could cause serious injury, illness or death — stop using it now.MKS Enterprise LLC
FDA (openFDA food enforcement)
Reported Aug 10, 2022
UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neotract Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use in the quantitative determination of iron in human serum and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
Merlin PCS 3650 programmer Model 3330 software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical, Cardiac Rhythm Management Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2022
Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack 4oz plastic bottles
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Procter & Gamble Company
4 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 3, 2022
REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, CE, R1 1 x 52 mL, R2 1 x 20 mL, A1cDL 2 x 35 mL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Bumble Bee Smoked Clams Shucked Easy Open NET WT. 3.75 oz. (106 g) Distributed By: Bumble Bee Seafoods San Diego, CA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bumble Bee Foods, LLC
FDA (openFDA food enforcement)
Reported Aug 3, 2022
Simply Nature Organic Spring Mix 16 oz. Marketside Spring Mix 11 oz. and 5 oz.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Aug 3, 2022
Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Description/Part: Simplify Disc Size 1, Ht 5/SM-5; Simplify Disc Size 1, Ht 6/SM-6; Simplify Disc Size 2, Ht 4/MD-4;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
10 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2022
SX-One MicroKnife
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sonex Health LLC
FDA (openFDA device enforcement)
Reported Jul 27, 2022
YelloPort Elite Universal Seal. For use in laparoscopic procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Surgical Innovations Ltd.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis US Corp.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Draeger Globe-Trotter and Globe-Trotter IC, Model numbers MS20508 and MS20509. neonatal transport system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical Systems, Inc.
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.