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Recalls distributed in Wisconsin

These notices name Wisconsin 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.

3,909 stored notices name Wisconsin, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Wisconsin too — those are in the archive.

Medical devices

Reported Jan 14, 2015

Cable remote control JUPITER U, Material no.4500119, Serial number: to (incl.) 102306915. Patient positioning during…

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

Trumpf Medical Systems, Inc.

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 7, 2015

Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro¿ Edge Safety…

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

Smiths Medical ASD, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2014

Bausch & Lomb Stellaris PC w/ Laser, BL14304 The responsible firm name is Bausch & Lomb Incorporated Rochester, NY

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

Bausch & Lomb Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2014

UroSeal Adjustable Endoscopic Valve. Model/Catalog # 00913410 The primary packaging is a Tyvek pouch. The secondary…

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

US Endoscopy Group Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2014

Aesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebrospinal fluid (CSF)…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Aesculap, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 24, 2014

Dark Cocoa Sorbetto packed in 14 oz. plastic jars, 8 packages per case, manufactured from 4/11/14-4/12/14; product…

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

House Of Flavors, Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 24, 2014

KOZY SHACK SIMPLY WELL CHOCOLATE, NET WT 4 OZ. Product packed in brown carton box, 48 individual units x 4 OZ. Keep…

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

Kozy Shack Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 24, 2014

RESTORIS PST Straight Shell Inserter An impactor is a reusable instrument designed for use by orthopedic surgeons…

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

Mako Surgical Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Food

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)

Medical devices

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)

Medical devices

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)

Food

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)

Food

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)

Medical devices

Reported Dec 17, 2014

Covidien Puritan Bennett 980 Ventilator, Rx ONLY, Made in Ireland., Covidien LLC, USA. REF 980X1ENDIUU.

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

Nellcor Puritan Bennett Inc. (dba Covidien LP)

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

BrightView XCT is a gamma camera for Single Photon Emission Computed Tomography (SPECT) and integrates with an…

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

Philips Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2014

Align Radial Stems, Prosthesis, Elbow, Hemi Replacement of the radial head for degenerative or post-traumatic…

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

Skeletal Dynamics

FDA (openFDA device enforcement)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

Reported Dec 3, 2014

Alfalfa seed: Organic, Alfalfa, NOP Oregon Tilth, Net Wt. 55 LB, International Specialty Supply

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

International Sprout Holding Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 3, 2014

Karlsburger Foods Taco Seasoning, Item Numbers 43823 (Packaged in 23 oz resealable plastic containers), Item #43807…

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

Karlsburger Foods, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 3, 2014

Kerry 52-0197-02, , Net Wt 39.7 lbs (18.00 Kg), B18516.01.

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

Kerry Foods

12 more products in this recall

FDA (openFDA food 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.