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.
3,963 stored notices name Wisconsin, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Wisconsin too — those are in the archive.
Reported Dec 9, 2015
Radiesse (+) Lidocaine Injectable Implant 1.5cc, P/N: 8063M0K1. Indicated for subdermal implantation for the correction…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 2, 2015
Daily Chef Peanut Butter Bars, Net Wt. 27 oz (1 lb 11 oz) 765g, Made in Canada, Manufactured for: CSM Bakery Products…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CSM Bakery Products NA
FDA (openFDA food enforcement)
Reported Dec 2, 2015
Meijer Caramel Corn, packed in 10 oz. bags, ( 283 g), 12 bags per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meijer Distribution, Inc.
FDA (openFDA food enforcement)
Reported Dec 2, 2015
Dimension Vista System (MG) ; Flex reagent cartridge Catalog number K3057, SMN 10445158. For the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 25, 2015
Dole All Natural SPINACH; Net Wt. 8 oz. (227 g). Enjoy by 10-15-15, UPC 7143000976 Product of the USA Excellent Source…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Nov 25, 2015
Hill-Rom 100 Low Bed (GPAC) AC Powered adjustable hospital bed
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2015
Kar's Sweet n' Salty Mix Box of 18, 3.5 oz. flexible film bags. 1 box per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kar Nut Products Company
10 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 25, 2015
Frozen Peas & Carrots, Product is IQF, frozen, not ready to eat, each label carries cooking instructions. Product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lakeside Foods, Inc.
FDA (openFDA food enforcement)
Reported Nov 25, 2015
PROVA, Standard Exhausted Vanilla Seeds, Graines VRAC, Caisses-outres of 50 X Lbs, packaged in a cardboard box.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prova Inc.
FDA (openFDA food enforcement)
Reported Nov 25, 2015
Synthes Application Instrument for Sternal ZIPFIX. Indications for use include primary or secondary closure/repair of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Nov 25, 2015
Taut Intraducers 10/BX7.5 FR 3.5, Product Code PI-93. To provide an access port into the peritoneal cavity.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Nov 18, 2015
RotaWire Elite and wireClip Torquer, Guidewire and Guidewire Manipulation Device, Floppy. REF H802223301 (5-pack outer…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 18, 2015
MILEX PESSARY KIT; Model Numbers: MXPES00; MXKPES00; MXKPREG03; MXKPGSK07 Product Usage: The Coopersurgical MILEX…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Medtronic Perfusion Tubing Packs, Models TL7M64R3, TL7P17R1 & HY2W85R9, Sterilized using Ethylene Oxide. The Tubing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Shimadzu C-arm Table, Catalog No. IVS-110, Medical Imaging Table.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Stryker Orthopaedics, MIS MODULAR DISTAL CAPTURE TRIATHLON MIS INSTRUMENTS, REF 6541-5-723, Lot AdminECR19205,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to provide additional support during fusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
FDA (openFDA device enforcement)
Reported Nov 18, 2015
SSS Reprocessed Zimmer, Synthes, Stryker and Linvatec Drill Bits and Blades Surgical drill bits, blades, burs, chisels,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Myelo-Nate CSF Sampling Kit, Neonatal/Pediatric cerebralspinal fluid sampling sterile tray, including a lumbar puncture…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Utah Medical Products, Inc.
FDA (openFDA device enforcement)
Reported Nov 11, 2015
The Centricity PACS-IW with Universal Viewer is a device that displays medical images (including mammograms) and data…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 11, 2015
MR Surgical Suite II Table, Model Number(s): M8074SS, M8053SS, M0074SS. UPDATE 11-4-2015: Model M0001SS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported Nov 11, 2015
Helioseal F Sealant Refill 1 x 1.25 g, REF 558519AN, and Helioseal F Assortment (kit) 5 x 1.25 g, REF 558518AN. Dental…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ivoclar A. G.
FDA (openFDA device enforcement)
Reported Nov 11, 2015
Robotic Arm Interactive Orthopedic (RIO) system component PN#205143 (locking pin) and PN# 112220 (connector). Indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Nov 11, 2015
GEMINI PET/CT System, a diagnostic imaging system for fixed or mobile installations that combines Positron Emission…
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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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.