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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.

4,253 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.

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

Reported Mar 12, 2014

*** 1) List number 126970465 labeled in part: 12697-65 LifeShield LATEX-FREE HEMA; Y-TYPE BLOOD SET, Nonvented, 88 Inch…

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

Hospira Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 12, 2014

Chocolate Ice Cream manufactured under the Dairy Rich brand and packaged in a 1.75 quart (1.66 L) (56 oz.) carton.

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

Ice Cream Specialities

FDA (openFDA food enforcement)

Medical devices

Reported Mar 12, 2014

Restoris Multicompartmental Knee (MCK) System is an implant system designed to be used with MAKO's Robotic Arm…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2014

McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects,…

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

Mckesson Technologies Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 12, 2014

Rise n Roll Bakery & Deli, White Powdered Donuts, sold individually and found in 6 count (436 g) UPC Code 6 26570 61744…

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

Rise'n Roll Bakery, LLC

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 12, 2014

Synthes 5.0mm Variable Locking Screw This device is part of the Variable Angle Locking Compression Plate family and…

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

Synthes, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2014

TSX-301C Aquilion One (Vision Edition) Computed Tomography X-Ray System.

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

Toshiba American Medical Systems Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 5, 2014

Bar Star Snack Mix, 1 lb plastic bag and 25 lb plastic bags in a cardboard box. Box labeled DAYTON'S ESTABLISHED 1923…

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

Creation Gardens

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 5, 2014

GE Healthcare - Giraffe Warmer;Panda Warmer;Panda iRes Warmer, Giraffe Stand-alone Infant Resuscitation System. Product…

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

GE Healthcare, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

VITROS Chemistry Products Na+ Slides, manufactured by Ortho Clinical Diagnostics 513 Technology Blvd Rochester, NY…

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

Ortho-Clinical Diagnostics

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2014

Single and Dual use Emission Computer Tomography gamma cameras (BrightView XCT, BrightView X & BrightView SPECT)…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

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Other states

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.