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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.

Medical devices

Reported Dec 4, 2013

SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED SIZE 1-1.5 HP M.B.T. Keel Punch Knee Instrument is used to…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DePuy Orthopaedics, Inc.

11 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 4, 2013

Mozzarella String Cheese made with 2% milk for 1/4 less fat, sold under Kraft brand or Polly-O brand and packaged with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Kraft Foods Group

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 4, 2013

2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recess 12 MM Fixation of fractures, osteotomies, nonunions,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Synthes USA HQ, Inc.

15 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

Juggerknotless Drill Bit, REF 110003173, Sterile, Single Use Product Usage: The Juggerknotless Soft Anchors are…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

GE Healthcare Discovery NMCT 670, Discovery NM 630, Optima NMCT 640, & Brivo NM 615. The GE Discovery NMJCT 670 system…

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)

Medical devices

Reported Nov 27, 2013

The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hospira Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50 dental adhesive for restorations

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ivoclar Vivadent, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300HS, CGRLS300S. CGRXT190HJ,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medtronic Vascular

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

VITROS Chemistry Products ACET Slides, 90 slides/pack; catalog number 1037274 VITROS Chemistry Products ACET Slides…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ortho-Clinical Diagnostics

36 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

Brilliance iCT Computed Tomography X-Ray System, Product Usage: The Brilliance iCT is a Computed Tomography X-Ray…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

EPIQ 7 Ultrasound System, Model 795200, 795201, 795202. Intended for diagnostic ultrasound imaging and fluid flow…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems North America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2013

Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to visualize upper airway and aid in placement of tracheal…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teleflex Medical

FDA (openFDA device enforcement)

Food

Reported Nov 27, 2013

Mixed nuts in a plastic bag labeled in part: PREMIUM QUALITY; Terri Lynn Inc.; Deluxe Mixed; No Peanuts; NET WT. 16 OZ.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Terri Lynn Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 27, 2013

Ready to Use Thymo-Cide, Germicidal Detergent, containing 0.051% thymol, packaged in 1-qt. bottles. The firm name on…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Wexford Labs Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2013

Sterrad 100NX, Product Code: 10104. Used to sterilize heat and moisture sensitive reusable medical devices.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Advanced Sterilization Products

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2013

SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP LCD screen, 55074-2 revision B) Product Usage:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2013

AW VolumeShare 4 (ADVANTAGE WORKSTATION 4.3.), AW VolumeShare 5 (AW VOLUMESHARE 5 WITH ANGIOVIZ OPTION), AW Server.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2013

Plum A+ Hyperbaric Infusion Pump; List Number 11005; Labeled in part: PLUM A+ HYPERBARIC; Product Usage: The Plum A+…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hospira Inc.

14 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 20, 2013

White grits packaged in a paper bag labeled in part: Smooth & Creamy; Aunt Jemima; Quick GRITS; Cooks in about 5…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Quaker Foods and Snacks North America

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 20, 2013

Fruit Truffles - Cherry, Coconut, Key Lime, Lemon, Mango, Pear, Pineapple and Tangelo flavors. (6 piece count/4.5 oz)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Torn Ranch Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 20, 2013

Titan 3T MRI System, MRT-3010A/5. Product Usage: Usage: MRI system.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Toshiba American Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2013

DRX Revolution, Catalog #'s 1)1019397, 2) 1023415 (w/ installation warranty, US-only) and 3) 1023423 (w/ parts…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carestream Health Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2013

Adjustable Gastric Band, packaged alone in transparent PETG inner and outer blisters with Tyvek lids, or in various kit…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ethicon Endo-Surgery Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2013

HAMILTON-C2 Ventilator: Manufactured by Hamilton Medical AG CH-7402 Bonaduz, Switzerland; Imported and distributed by…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hamilton Medical, 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.