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 Dec 30, 2020
Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Ortho-Med Inc.
FDA (openFDA device enforcement)
Reported Dec 23, 2020
Carl Zeiss Meditec Ag VISULENS 550 REF 2268-038 - Product Usage: is a device for measuring the refractive power of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 23, 2020
Outshine Fruit & Cream Bars - Creamy Pineapple Coconut 6 fruit and dairy bars, 14.7 fl. oz. UPC: 41548 91817 4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dreyers Grand Ice Cream, Inc.
FDA (openFDA food enforcement)
Reported Dec 23, 2020
Kowa VK-2s software Version 10.0.4.0, Product code 04987646809500 installed on Kowa nonmyd WX Retinal Cameras - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kowa Optimed Inc.
FDA (openFDA device enforcement)
Reported Dec 23, 2020
Tina-quant C-Reactive Protein Gen.3, Catalog number 05172373190 - Product Usage: the in vitro quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Dec 16, 2020
BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Usage: intended as a complete process control for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Dec 16, 2020
MAC VU360, Electrocardiograph
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Dec 16, 2020
Shimadzu Mobile X-Ray System, MobileDaRt Evolution (MX8 Version), with adjustable handle option, Made in Japan -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 16, 2020
Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Ltd.
FDA (openFDA device enforcement)
Reported Dec 16, 2020
HomeChef Meal kit:One-Sheet Pretzel-Crusted Chicken with roasted broccoli and honey mustard..31.0 OZ (1 LB 15 OZ) 879g
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Kroger Co.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 16, 2020
PROKERA, non-sterile - Product Usage: Biologic corneal bandage.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TissueTech, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 16, 2020
ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Welch Allyn, Inc/mortara
FDA (openFDA device enforcement)
Reported Dec 9, 2020
Tizanidine Tablets, USP 4mg, Rx Only, 150 Tablets per Bottle, Manufactured by Alkem Laboratories Ltd, Mumbai - 400 013,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascend Laboratories LLC
FDA (openFDA drug enforcement)
Reported Dec 9, 2020
MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric Model MX60ET - Product Usage: The lens is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
FDA (openFDA device enforcement)
Reported Dec 9, 2020
CME America T-Syringe Pump -T34L - Product Usage: infusion of medications or fluids requiring continuous or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CME America, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 9, 2020
Dole" Organic Romaine Hearts 3pk Organic Biologique) (UPC 0-71430-90061-1), Wild Harvest Organic Romaine Hearts, Net Wt…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Dec 9, 2020
Tanimura & Antle brand Romaine lettuce. 1 head 12,15,018 and 24 case Product of USA UPC: 2-27918 20314-9 Tanimura &…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tanimura & Antle
FDA (openFDA food enforcement)
Reported Dec 9, 2020
BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coloplast Manufacturing US, LLC
FDA (openFDA device enforcement)
Reported Dec 2, 2020
EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the Ion Fully…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
ViewRay MRIdian System: Model No. 10000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viewray, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Art Of Tea - Feel Better tea; Produced and Distributed by: Art of Tea LLC, Monterey Park, CA Directions: 1 Tbsp of tea…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Art Of Tea
FDA (openFDA food enforcement)
Reported Nov 25, 2020
VNS Therapy¿ AspireSR¿ Generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA 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.