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 Nov 6, 2013
Schwebel's Golden Rich Bun with Honey, 18 oz plastic bag, 12 count, UPC 0 71319 00083 8 Product labeled in part,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Schwebel Baking Company
FDA (openFDA food enforcement)
Reported Nov 6, 2013
pocH-100i; sysmex; Automated Hematology Analyzer; 7.3" x 13.8" x 18.1" / 30.8 lbs.; Sysmex Corporation; 1-5-1…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sysmex America Inc.
FDA (openFDA device enforcement)
Reported Oct 30, 2013
Synergetics 25 gauge Soft Tip Cannula, packaged in 6 units per box. Catalog number: 30.08.25. Single-use 25 gauge…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synergetics Inc.
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Getinge 46-Series Medical Washer-Disinfectors, Listing # E208196 Product Usage: The washer disinfector is used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge Disinfection
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Harvest Graft Delivery System; Model Number: GDP-10 Product Usage: The Harvest Graft Delivery System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Harvest Technologies Corporation
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Brilliance CT Big Bore Oncology, Brilliance CT Big Bore Radiology and Brilliance CT 16 (Air) Brilliance CT Big Bore…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Dimension Vista (R) Urinary/Cerebrospinal Fluid Protein (UCFP) Flex (R) Reagent Cartridge Lot 11349BB The Urinary /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Synthes Midfoot Fusion Bolt 6.5 mm. It is indicated for fracture, fixation, osteotomies, nonunions, and fusions of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
FDA (openFDA device enforcement)
Reported Oct 9, 2013
Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular introduction of interventional and/or diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Oct 9, 2013
Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The intended use is in vitro testing of samples of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Oct 2, 2013
BD Epilor Syringe BD Franklin Lakes, NJ 07417 BD EDC Laagstraat 57, B-9140 Temse-Belgium The Epilor syringe is used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Monaco RTP System Radiation treatment planning
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2013
spartan fresh selections american potato salad, Net Wt. 16 oz (1 LB) 454g. UPC 11213-90320.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Garden-Fresh Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 2, 2013
Breaded, frozen shrimp packaged in plastic bags labeled in part: BREADED SHRIMP; NET WEIGHT; 2.0 LBS or 3 LBS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gourmet Express Marketing, Inc.
FDA (openFDA food enforcement)
Reported Oct 2, 2013
Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Meijer 8 Inch Carrot Uniced Split Cake Layers (product is packed in bulk cartons of 24 units/paper bags lined with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maplehurst Bakeries, Inc.
FDA (openFDA food enforcement)
Reported Oct 2, 2013
Smith Medical, Deltec, REF 21-2386-24, 11 Fr Introducer Set with Peel-Away Sheath, Sterile EO, Rx Only PORT-A-CATH¿ and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Stryker Vision Mounting Arm, for use with other Stryker Endoscopy medical device products for human patients. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Endoscopy
FDA (openFDA device enforcement)
Reported Oct 2, 2013
The FL23SE Bed is an AC-powered adjustable hospital bed with four built-in electric DC motors and remote controls that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Terumo Pall AL6X Arterial Blood Line Filter, labeled in part Terumo Cardiovascular Systems Corporation, packaged as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Sep 25, 2013
3M Scotchcast, Wet or Dry Cast Padding, Catalog Numbers WDP2, WDP3, WDP4, and WDP6. Intended for use in constructing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Sep 25, 2013
POWERWAND Safety Introducer with Extended Dwell Catheter; Catalog no. 92006. Used to gain access to the vascular system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Access Scientific Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
DiaScreen Liquid Urine Controls: Positive and Negative Assayed Liquid Quality Controls for use with Dipsticks in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Assuramed
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Blanketrol III, Model Number 233, Cincinnati Sub-Zero Products, Inc., 12011 Mosteller Road, Cincinnati, OH 45241…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products 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.