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 18, 2021
Covidien Sonicision Reusable Generator-converts electrical power from the battery pack to ultrasonic energy to drive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Edwards PediaSat Oximetry Catheter Kit, REF: XT3515KTP, Exterior Diameter 5.5F (1.83 mm), Usable Length 15 cm, Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Zyprexa Intramuscular, Olanzapine for Injection, 10 MG per Single Use Vial, Rx only, Marketed by: Lilly USA, LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eli Lilly & Company
FDA (openFDA drug enforcement)
Reported Aug 18, 2021
Medtronic StimLoc Burr Hole Cover, Part Numbers: a) 3387S-40 b) 3389S-28 c) 3389S-40 d) 3391S-40 e) 3550S-01 f) 924256…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 18, 2021
MOLLY & ME PECANS all natural PRALINE PECANS, 4 oz., 7 oz., and 12 oz packages, INGREDIENTS: Pecans, Brown Sugar,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Molly and Me Pecans
FDA (openFDA food enforcement)
Reported Aug 18, 2021
CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard Wolf GmbH
FDA (openFDA device enforcement)
Reported Aug 11, 2021
Beta-Hydroxybutyrate LiquiColor. in vitro diagnostic reagent.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stanbio Laboratory, LP
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 11, 2021
GlideScope Go Monitors
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Del Monte Fresh Cut Golden Sweet Whole Kernel Corn; 15.25 oz. can (24 x 15.25 oz. cans per case) Case UPC …
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 4, 2021
Backcountry Dried Apricots 9ounce plastic bag 12 packages per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods Operating Company, LLC.
FDA (openFDA food enforcement)
Reported Aug 4, 2021
basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Used to inflate and deflate an angioplasty balloon or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Now Real Food Organic Steel Cut Oats, 2 lb bag, code 6295, UPC 733739062956, packed 8 bags per case; case packaging is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NOW Health Group Inc.
FDA (openFDA food enforcement)
Reported Aug 4, 2021
ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported Aug 4, 2021
Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sunrise Medical (US) LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2021
Greater Omaha Packing Recalls Raw Beef Products Due to Possible E. Coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Greater Omaha Packing Co., Inc.
USDA FSIS
Reported Jul 28, 2021
Suture Anchor, BioComposite SwiveLock C, 5.5 mm x 19.1 mm, Closed Eyelet, REF AR-2323BCC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Kroger brand, Vitamin D3 125 mcg softgels, 100 count, Green HDPE packaging
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Bountiful Trading Inc.
FDA (openFDA food enforcement)
Reported Jul 28, 2021
Infant Heel Warmer with Attachment Tab, Nonsterile, Active Product SKU MH00002T The infant heel warmer is activated at…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Disposable Replacement Backflush Brush Needles (23 gauge/0.6mm)-for use in vitreoretinal surgery Product Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dutch Ophthalmic USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Extra Large Premium Cotton Ovals - two textures soft…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Respironics California, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 21, 2021
Toshiba Vantage Tiitan 1.5T with Standard gradient, Premium Open-Bore MRI System, REF: MRT-1504 - Product Usage: use as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 21, 2021
Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jul 21, 2021
Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only
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)
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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.