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 48,122 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Dec 24, 2014
SOLGAR ENHANCED SERIES ABC DOPHILUS POWDER FOR INFANTS AND CHILDREN, NET WT. 1.75 oz (50 g), UPC 0 33984 00010 0.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.NBTY, Inc.
FDA (openFDA food enforcement)
Reported Dec 24, 2014
Additional devices identified in new FSN MA-FCO 83000190: QLAB versions 10.0 with a2DQ and/or aCMQ plug-ins installed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2014
Specialty Audible Torque Wrench Mfg by: Stryker Spine, Catalog number IS3002XLP, Non-sterile. Used to final tighten to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Conformis iTotal CR G2 Knee Replacement System Catalog/Model #: M57250600010 Intended for use as a total knee…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConforMIS, Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Invacare Perfecto 2 V Oxygen Concentrator The finished device is packaged as a single unit. The service part contains a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Chicken flavored broth base and seasoning, low sodium sold under the Orrington Farms brand in 5 oz. plastic jars.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kent Precision Foods Group, Inc.
FDA (openFDA food enforcement)
Reported Dec 17, 2014
ESSENTIA Hydration Perfected Purified Water and Electrolytes, 9.5 pH, Manufactured for Essentia Water Inc., 22833…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nature's Way Purewater Systems, Inc.
FDA (openFDA food enforcement)
Reported Dec 17, 2014
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snug Seat Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2014
TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / 2.0.3/ (Hi:Art 5.0.1 / 5.0.2 / 5.0.3)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TomoTherapy Incorporated
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Amerigel Hydrogel Wound Dressing Wound management
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 10, 2014
MAS CardioImmune XL Cardiac Marker Control; Model: CAI-XL1; intended for use in the clinical laboratory as an assayed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 or 4 Bottle(s) (6.6 mL/27.0 mL) anti-T3 (sheep) coated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
FDA (openFDA device enforcement)
Reported Dec 3, 2014
8MM,POTTS SCISSORS; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
21 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
LUNA Chest, Model No. LU4006
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novadaq Technologies, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 26, 2014
CyberKnife Robotic Radiosurgery System with the first generation IRIS Variable Aperture Collimator. The CyberKnife is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accuray Incorporated
FDA (openFDA device enforcement)
Reported Nov 26, 2014
Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Biomerieux
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 26, 2014
LANX, REF, PCR8XXX-XXX, LOT, RXONLY. Packaged within aluminum sterilization case. Product Usage: The Durango implant is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet Spine LLC.
FDA (openFDA device enforcement)
Reported Nov 26, 2014
Edwards Lifesciences Vent Catheters, . Packaged sterile and non-pyrogenic in a sealed, peel-type pouch. Model Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 26, 2014
Mt. Olive, Kosher Dill Chips in 1 gallon glass jars, UPC 09300 12841, Mt. Olive, Corner of Cucumber & Vine, P.O. Box…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mt. Olive Pickle Company Inc.
FDA (openFDA food enforcement)
Reported Nov 26, 2014
Transport Chair and Rollator in 1, Model HE21630011 Burgundy and HE21630011 Blue. This is a walker/rolling chair. Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Silver Star Brands
FDA (openFDA device enforcement)
Reported Nov 26, 2014
AxoTrack I Sterile Procedure Kit 18G, K1001-18XTW, (24/case labeled for US, 5/case labeled for US, 24/case labeled for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Soma Access Systems LLC
FDA (openFDA device enforcement)
Reported Nov 19, 2014
AMS 700 Series Inflatable Penile Prosthesis Accessory Kit (AMS 700 Line Accessory Kit), 72401850. Keith Needles are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Medical Systems, Inc.
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.