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.
4,312 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Apr 2, 2014
Thickened Water Pudding Thick 32 oz. (944ml) Phase 3 Ingredients: Pasteurized Filtered Water, Cellulose Gum Fibre,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutra Balance Products
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 2, 2014
Siemens Artis Q and Artis Q biplane systems Product Usage: Interventional Fluoroscopic X-ray
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 2, 2014
Drill Template and the Saw Guide for the Ulna Osteotomy System. Intended for fixation of fractures, osteotomies,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Apr 2, 2014
HeartMate II Implant Kit with Pocket Controller; with sealed grafts (NAm) with sealed grafts (EU) Product Usage:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Thoratec Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 2, 2014
DICOM Export Format for Sum Dose with Velocity v3.0.0. A stand-alone software product that provides the oncology care…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Velocity Medical Solutions, LLC
FDA (openFDA device enforcement)
Reported Apr 1, 2014
Oklahoma Firm Recalls Chicken Products Due To Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.AdvancePierre Foods, Inc.
USDA FSIS
Reported Mar 26, 2014
SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for radiation therapy treatments of malignant neoplastics…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 26, 2014
4 oz. Heart - Shaped Box of Assorted Chocolates
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fannie May Confection Brands Inc.
FDA (openFDA food enforcement)
Reported Mar 26, 2014
GE Healthcare Optima CT580/Discovery CT590RT scanners running software version 13BW16.3. The Discovery CT 590 RT and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Mar 26, 2014
syngo Dynamics Picture Archiving and Communication System (PACS). Model numbers 10091804, 10091805, 10091806, 10091807,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Mar 26, 2014
2.5MM Aggressive Blade Known as a Sinuscopic Shaver Blade, this device is composed of a metal cutter and plastic drive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses commonly associated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Sarns Malleable Dual-stage Venous Return Cannulae, 28/38 Fr with 1/2" connector, 14.5" (37 cm) long The Sarns Malleable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Gender Solutions" Natural-Knee¿ Flex System: N-K FLEX MBACK SZ 0 PAT N-K FLEX MBACK SZ 1 PAT N-K FLEX MBACK SZ 2 PAT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
bioMerieux PREVI Isola System (General purpose,microbiology, diagnostic Medical Device), (REF 29500/29500R),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2014
XiO RPT System The XiO RTP System is used to create treatment plans for any cancer patient for whom external beam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2014
Jalapeno Ground 40, Elite Spice Code #JP9520, 50 lb poly-lined cartons labeled in part ***Elite Spice Inc. 7151…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Elite Spice Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 19, 2014
GE Healthcare, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ Innova 2121IQ, Innova 3131IQ;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
Markets of Meijer Pretzel Hamburger Bun, 4 count, NT.WT. 12.0 oz (0.75 lb), 16 oz ( 1 lb) UPC 412500558-2; Ingredients:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Meijer Distribution, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 19, 2014
4040-2: Umbilical 3 mL Line Draw, Luer lock syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2014
All Elekta digital accelerators with electrons and beam modulator, MLCi/MLCi2, Agility or Asymmetric Heads Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2014
GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version 5.4, 5.5, or 5.6 with the Automatic-View-On-…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2014
Greatbatch Medical, Offset Cup Impactor. Part Numbers: P9485, T10243, T10281, T10287, T10484, T10491, T10507, T10600,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Greatbatch Medical
FDA (openFDA device enforcement)
Reported Mar 12, 2014
BencoDental tartar & stain remover ultrasonic cleaning solution Product Usage: Formulated especially for removal of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heraeus Kulzer, 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.