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 Jan 12, 2022
Biomeme SARS-CoV-2- Real Time RT-PCR Test, Instructions for Use, Part number 100002824 Subcomponent of: SARS-CoV-2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomeme, Inc.
FDA (openFDA device enforcement)
Reported Jan 12, 2022
Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
Reported Jan 12, 2022
DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medshape, Inc.
FDA (openFDA device enforcement)
Reported Jan 12, 2022
Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An automated, clinical chemistry analyzer designed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jan 5, 2022
iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States);…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AMO Manufacturing USA, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 5, 2022
RAPID 20 E, REF 20701, System for the identification of Enterobacteriaceae in 4 hours, 25 strips/package, IVD.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Jan 5, 2022
Giant Eagle Diced Green Peppers, 10 oz. 283 g, Frozen bag, 12 packages per case , Best By 10/14/2023 .
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Giant Eagle, Inc.
FDA (openFDA food enforcement)
Reported Jan 5, 2022
Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Dec 29, 2021
TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acclarent, Inc.
FDA (openFDA device enforcement)
Reported Dec 29, 2021
WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported Dec 29, 2021
Skinny Needle with Chiba Tip. RPN 090010, 090010-ET; GPN G14254, G15290. Rigid needle available with EchoTip to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Dec 29, 2021
Leica Microsystems M220 F12 Microscope Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Dec 29, 2021
Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Navigation, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 22, 2021
Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Activ5 User Manual: ACTIV5 USER MANUAL Welcome to Activ5,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Activbody, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 22, 2021
Krispy Kreme DOUGHNUT Bites ORIGINAL GLAZED 5 1.6 OZ (45g) POUCHES NET WT. 8 OZ (227g) Manufactured under the authority…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Krispy Kreme Doughnut Corporatio
FDA (openFDA food enforcement)
Reported Dec 22, 2021
MENTOR Saline-Filled Breast Implants are constructed from room temperature vulcanized silicone elastomer, made of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mentor Texas, LP.
FDA (openFDA device enforcement)
Reported Dec 22, 2021
Miami J Select Collar, Item: MJS-101, and Miami J Select Collar Set, Item: MJSR-101 Instructions for Use
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Dec 22, 2021
The Mustard Man Inc Simply Peppered Mustard 8oz plastic bottles, 6 bottles per case
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Mustard Man Inc.
FDA (openFDA food enforcement)
Reported Dec 15, 2021
SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Dec 15, 2021
Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mountain Meadow Herbs, Inc.
FDA (openFDA food enforcement)
Reported Dec 15, 2021
O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing Instructions (model preparation for tooth…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orchestrate Orthodontic Technologies, Inc.
FDA (openFDA device enforcement)
Reported Dec 15, 2021
OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 REF 450-0021-00 -OsteoMed D-Power Control…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Osteomed, LLC
FDA (openFDA device enforcement)
Reported Dec 15, 2021
Trader Joe's Organic Blue Corn Tortilla Chips: 16 oz. bag, 15 bags per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trader Joes Company
FDA (openFDA food enforcement)
Reported Dec 8, 2021
BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
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.