Recalls distributed in Michigan
These notices name Michigan 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.
4,580 stored notices name Michigan, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Michigan too — those are in the archive.
Reported Jan 27, 2016
FMS neXtra¿ 3.5mm Full Radius Cutter Shaver Blades; Product Code: 283305 Intended to provide controlled cutting,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 27, 2016
Fukuda Denshi patient monitor model DS-8100M and DS-8100N. The Fukuda Denshi DynaScope Model DS-8100N/8100M Patient…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fukuda Denshi USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 20, 2016
Medrad Source Administration Sets, Catalog number INT CSS. For use with MEDRAD Intego PET Infusion pump Systems, in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Healthcare
FDA (openFDA device enforcement)
Reported Jan 20, 2016
UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response 5.5/6.0 Spine System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Jan 20, 2016
Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skytron, Div. The KMW Group, Inc.
FDA (openFDA device enforcement)
Reported Jan 20, 2016
Reprocessed Stryker Color Cuff and Color Cuff II Adult Tourniquet Cuffs Model Numbers: 5921-218-135, 5921-044-135,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Jan 20, 2016
TWININGS OF London ENGLISH BREAKFAST BLACK TEA DECAFFEINATED, 12-0.11OZ (3.2g)/ EA NET WT 1.34 oz (38g), UPC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Twinings North America, Inc.
FDA (openFDA food enforcement)
Reported Jan 20, 2016
Zimmer, Virage OCT Spinal Fixation System, Item Number: 07.01738.001, a posterior system intended to achieve an implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 13, 2016
CNSystems TASK FORCE MONITOR 3040i, plethysmograph, impedance. Noninvasively measure and display patient's hemodynamic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Partners In Medicine LLC
FDA (openFDA device enforcement)
Reported Jan 13, 2016
Software version VD10E for Syngo X-Workplace; Picture archiving and communication system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 13, 2016
BAKERY FRESH GOODNESS Chocolate Brownie NET WT 16 OZ (1 LB) 453 g CONTAINS: MILK, EGGS, WHEAT, SOY. MAY CONTAIN:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
FDA (openFDA food enforcement)
Reported Jan 6, 2016
Barilla MEDIUM SHELLS, 1 LB (454 g), GTIN 00076808002881, packed as twelve boxes in 1 case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Barilla America NY, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 6, 2016
Radiographic Transparency for Certain and External Connection Tapered Implants. Images that assist with measurements…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
FDA (openFDA device enforcement)
Reported Jan 6, 2016
Friendly Farms Greek Peach Parfait Nonfat Yogurt net wt. 5.3 oz (150g) Distributed by ALDI Inc., Batavia, IL 60510
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ehrmann Arizona Dairy LLC
FDA (openFDA food enforcement)
Reported Jan 6, 2016
MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jan 6, 2016
Baker's Best Maximum Mind & Memory Formula, 60 capsules, Vitamin B6 75 mg. Distributed by Baker's Best Health Products,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pure Source, Inc.
FDA (openFDA food enforcement)
Reported Dec 30, 2015
Vancomycin Screen Agar
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Biomerieux
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2015
A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization and fixation of fractures, revision…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2015
IntellaTip MiFi XP Asymmetric (N4) Curve, 7/110/2.5/8-8 OUS; Material Number: M004EPM4500N40; Catalog number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Boston Scientific, Chariot ST-CCV Guiding Sheath, Sterilized using ethylene oxide: Product Description Material Number…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Aegis Torque Handle CATALOG NO. : 2871-10-800. A spinal surgical instrument used on the AEGIS Anterior Lumbar Plate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Spine, Inc.
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Optional PS500 Power Supply Unit for the Evita V500 Ventilator and Babylog VN500 Ventilator. Babylog VN500 is a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Double Trigger Handpiece. Rx only Made in Switzerland
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)
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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.