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 Jun 4, 2014
ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35); ultrasound imaging system.
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 May 28, 2014
GE Healthcare, NeuroMuscular Transmission Module, E-NMT-01 Product Usage: The Datex-Ohmeda S/5TM E-NMT module is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported May 28, 2014
Verdex Fresh Snow Peas packed in 10 pounds cartons, keep refrigerated, Lot # 2161100811 product from Guatemala
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Harvest Sensations LLC
FDA (openFDA food enforcement)
Reported May 28, 2014
Gluma Desensitizer Power Gel Product Usage: Usage: This is a class 2 medical device. For reduction or elimination of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heraeus Kulzer, LLC.
FDA (openFDA device enforcement)
Reported May 28, 2014
LATEX-FREE; EXTENSION SET; For Bladder Irrigation or Urinary Drainage, Compatible with T-U-R FLOW-POUCH RESERVOIR, list…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported May 28, 2014
Esmark Elastic Bandage (Sterile), 4" x 9'. Item DYNJ05116A, Individually wrapped, 20 bandages per case. Packaged by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported May 28, 2014
Blue Bunny Premium Ice Cream, Bordeaux Cherry Chocolate, 1.75 quart. Packaged in 4/56-oz carton cases. Item # 745152,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wells Enterprises, Inc.
FDA (openFDA food enforcement)
Reported May 21, 2014
HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) - HeartWare Battery For use as a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartWare Inc.
FDA (openFDA device enforcement)
Reported May 21, 2014
Private Selection Chocolate Hazelnut Mascarpone Ice Cream, 16 fl oz lamented carton. Product labeled in part, "PRIVATE…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 21, 2014
Enaly 1000 BT-12 Ozone Generator, Model # 1000BT-12 The 1000BT-12 ozone generator is capable of delivering up to 1gram…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.William C. Domb, D.M.D., A Professional Corporation
FDA (openFDA device enforcement)
Reported May 21, 2014
DROP LOK" Knee Brace***LATEX FREE" Product Usage: Used in the treatment, support, and rehabilitation of many types of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 14, 2014
PRIVATE SELECTION SWEET STRAWBERRY SORBET, Labeled in part: "INGREDIENTS: WATER, SUGAR***DISTRIBUTED BY, THE KROGER…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Co.
FDA (openFDA food enforcement)
Reported May 14, 2014
Mar Cor Purification, Central Water Platform (CWP), 102, 104 and 106. Product Usage: The CWP is a Central reverse…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mar Cor Purification
FDA (openFDA device enforcement)
Reported May 14, 2014
Nonabsorbable Surgical Suture, U.S.P., Sterile - Do Not Resterilize, Deknatel. Indicated for use in soft tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 7, 2014
ExacTrac 6.0 is a patient positioning and monitoring system. Model/catalogue numbers: 20833B EXACTRAC 6.0 IR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported May 7, 2014
GE Healthcare, CardiacVX [CardiacVX (1.1.0 Ext. d) and CardiacVX Flow (1.1.0 Ext. d) analysis software running 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 May 7, 2014
Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 3, 2014
Missouri Firm Recalls Curry Chicken Salad for Possible Listeria Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Missouri Firm
USDA FSIS
Reported Apr 30, 2014
The CEP 8 SpectrumGreen (SG) ASR Probe Kit, 20ul (list 06J37-018) is an Analyte Specific Reagent (ASR) containing a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Molecular
FDA (openFDA device enforcement)
Reported Apr 30, 2014
ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
ev3 EverCross 0.035" OTW PTA Dilatation Catheter, 6mm x 120mm x 135cm, REF: AB35W06120135. and ev3 EverCross 0.035" OTW…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ev3, Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device) Catalog Numbers: 1100, 1101, 1102, 1103, 1104,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2014
LifeShield LATEX-FREE HemoSet 100 mL Burette I.V. PlumSet, Nonvented, 105 inch with Prepierced Reseals, OPTION-LOK and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Stryker PenAdapt"; Rx Only, Sterile. This device is an accessory to an electrosurgical unit (ESU). The PenAdapt is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
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.