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.
4,309 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Jan 22, 2020
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Siemens ARTIS pheno, Model # 10849000. Interventional Fluoroscopic X-Ray System - Product Usage: Angiography system for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2020
Cochlear Baha 5 Sound Processor Tamper Proof Battery Door (3 pcs.)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cochlear Americas Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2020
Simply Fresh brand MiniMeals2Go Protein Pack (8.25 OZ) ready-to-eat snack packs
High riskUsing this product could cause serious injury, illness or death — stop using it now.Five Star Gourmet Foods
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 15, 2020
Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries, Inc. 306
FDA (openFDA device enforcement)
Reported Jan 15, 2020
GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TFI Holding dba Grey Ghost Bakery
FDA (openFDA food enforcement)
Reported Jan 8, 2020
i-STAT cTnI cartridge
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
FDA (openFDA device enforcement)
Reported Jan 8, 2020
Blood Glucose Monitoring System, Model Number 07400870001 ACCU-CHEK GUIDE SAMPLE KIT MG/DL - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2020
HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
Juno DRF, Model Number 709020 - Product Usage: General. multi-function x-ray systems capable of routine radiographs and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Sistemi Medicali S.P.A.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
STA UNICALIBRATOR (ref. 00675)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
Trader Joe's 8pcs Spicy California Roll, 8oz, SKU 00348966T
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fuji Food Products, Inc.
22 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2020
VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy
High riskUsing this product could cause serious injury, illness or death — stop using it now.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mazor Robotics Ltd.
FDA (openFDA device enforcement)
Reported Jan 1, 2020
7% BSA (Bovine Serum Albumin), Product Code: 8262487 - Product Usage: is used to dilute samples when assay values…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho Clinical Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2020
PTS Panels CHOL+HDL+GLU Test Strips, Reference Number 5412, for use on CardioChek PA or CardioChek Plus analyzers
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymer Technology Systems, Inc.
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Allergan PLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2019
A1CNow+ Systems (professional use product), Software Version Revision D, REF Numbers US: 3021, 3024; EU: 3037, 3038,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymer Technology Systems
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2019
Truly Good Foods SOUTH OF THE BORDER nut mix NET CT/WT: 25lb box, CONTAINS: PEANUTS, MILK, AND WHEAT. Distributed by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tropical Nut & Fruit Company
FDA (openFDA food enforcement)
Reported Dec 18, 2019
Healix Knotless ADV BR 4.75 Suture Anchor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Monaco Radiation Treatment Planning System (RTP) System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
EMPOWR Locking Femoral Impactor , Part # 800-05-035, packaged in instrument tray FA EMP PAT TOOL KIT Part # 800-99-096
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Terra Alba Calcium Sulfate Dihydrate packaged in 50 lb. bags; 25 lb. bags; 800kg (1764 lb.) bulk bags; 2000 lb. bulk…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Harrison Gypsum, LLC
FDA (openFDA food 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.