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 48,100 notices were distributed nationwide, so they reach Michigan too — those are in the archive.
Reported Jan 5, 2024
FSIS Issues Public Health Alert For Frozen Mushroom Risotto Products Due To Misbranding And Undeclared Allergen
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Reported Jan 3, 2024
Alinity ci-series System Control Module, REF: 03R70-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jan 3, 2024
RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320, Low Profile Primary Guide is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Jan 3, 2024
Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Abbott CELL-DYN Ruby, Model CD-Ruby, List number 08H67-01, and Abbott CELL-DYN Sapphire, Model CD Sapphire, list number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Biolox Ceramic Option Head Zimmer 12/14 40mm -3, Item Number 00-8777-040-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Injection Needle, REF: 25207
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Kwik Trip Cantaloupe, Item 930541. Net Wt 6 oz (170g). UPC 0 39779-00213 7. Produced & Distributed by Kwik Trip Inc.,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kwik Trip, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 27, 2023
0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nurse Assist, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 27, 2023
ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI USA Elite System and USA Series Right Angle Cutting…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Dec 27, 2023
The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Dec 27, 2023
AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Dec 27, 2023
LITe Decompression Snake Arm, REF 48080230
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Spine
FDA (openFDA device enforcement)
Reported Dec 27, 2023
Bulk Frozen Cases: The 9" Vegan Pumpkin Pie bulk case has UPC 22518 84081 and the label is read in parts: 9" Vegan…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Willamette Valley Pie Company, LLC
FDA (openFDA food enforcement)
Reported Dec 27, 2023
ZEUS ELISA Parvovirus B19 IgG Test System, Product Number SM9Z7701M
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zeus Scientific, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 20, 2023
Sienna Bakery Chocolate Decadent Brownies (Tray)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dianne's Fine Desserts
FDA (openFDA food enforcement)
Reported Dec 20, 2023
Deli Express, Deli Club 4.4oz wedge sandwich, 10 retail units per wholesale case, UPC 41433-00157
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.E.A. Sween Co.
FDA (openFDA food enforcement)
Reported Dec 20, 2023
Gaw's Deluxe Italian sub 12oz, Foam Tray with Clear Plastic Wrap package, UPC:1725600910
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gaws Gourmet Foods
4 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 20, 2023
Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Houdini Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 20, 2023
TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Dec 20, 2023
Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips North America LLC
FDA (openFDA device enforcement)
Reported Dec 20, 2023
ARTIS icono (ceiling configuration), Fluoroscopic x-ray system; Model no. 11328100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Dec 20, 2023
Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX REF 420-159 Spectranetics Turbo-Elite Laser Atherectomy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Dec 13, 2023
Atrium Firm PVC Thoracic Catheter 36FR Straight, part number 15036.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
2 more products in this recall
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.