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 May 29, 2019
Losartan Potassium Tablets USP 25 mg 30 count bottle NDC 60429-316-30 Rx only GSMS Incorporated
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Golden State Medical Supply Inc.
4 more products in this recall
FDA (openFDA drug enforcement)
Reported May 29, 2019
DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driven sensor which is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.KaVo Dental Technologies LLC
FDA (openFDA device enforcement)
Reported May 29, 2019
VITROS XT 7600 Integrated System, with V3.4 or 3.4.1 SW Product Code: 6844461 Product Usage: INTENDED USE: For in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported May 29, 2019
Thio Med w/Dex, Hem, Vit K (5ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported May 29, 2019
Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
75 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Compass Health Brands (Corporate Office)
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2019
CS011 GNR PNA FISH Control Slide, manufactured as a component of the CS011-10 GNR PNA FISH Control Slide kit . In-Vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Opgen Inc.
FDA (openFDA device enforcement)
Reported May 22, 2019
Artis Zee (material # 10094135, 10094137, 10094141) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 21, 2019
BEF Foods, Inc. Recalls Beef Products Produced without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.BEF Foods, Inc.
USDA FSIS
Reported May 17, 2019
Caito Foods LLC. Recalls Salads with Chicken Products due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Caito Foods, LLC
USDA FSIS
Reported May 15, 2019
Neuro Omega System, incorporating HaGuide software. For neurological and neurosurgical use. To monitor, record and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Alpha Omega Engineering
FDA (openFDA device enforcement)
Reported May 15, 2019
El Guapo Chile Habanero Habanero Chili Pepper 0.5oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCormick & Company, Inc. - Flavor Manufacturing Center
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 15, 2019
Atellica IM 1300 Analyzer, Material Number 11066001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 15, 2019
Dragonfly Dehydrate Guava Ing: Guava, Sugar, Salt Net Wt: 5.25 ozs 150g Distributed by: U.S. Trading Company Product of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.U.S. Tov, Inc.
FDA (openFDA food enforcement)
Reported May 15, 2019
T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Biomet Headless Compression Screws and Twist-Off…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 8, 2019
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), product code 35700BAX - Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported May 8, 2019
FilmArray Gastrointestinal (GI) Panel, IVD, Rx Only, Biofire Diagnostics, LLC REF: RFIT-ASY-0104, and RFIT-ASY-0116),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported May 8, 2019
Lamb s Supreme Potato Tater Puffs, item # H30, packaged in 5-pound unprinted KRAFT paper bags, 6 bags to a case, sold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lamb Weston BSW LLC
FDA (openFDA food enforcement)
Reported May 8, 2019
Ethyl Alcohol Enzymatic Assay, (a) REF 0220 (small test kit), (b) REF 0221 (large test kit) Product Usage: Detergent…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Lin-Zhi International Inc.
FDA (openFDA device enforcement)
Reported May 8, 2019
cobas e 801 immunoassay analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
FDA (openFDA device enforcement)
Reported May 8, 2019
MRIdian Linac Radiation Therapy System, Model 20000.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viewray, Inc.
FDA (openFDA device enforcement)
Reported May 1, 2019
St. Jude Medical Confirm Rx Insertable Cardiac Monitor, REF DM3500, Sterile. Product Usage: The St. Jude Medical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott
FDA (openFDA device enforcement)
Reported May 1, 2019
Arthrex Burr, Oval, 12 Flute, 5.5 mm x 13 cm (AR-8550OBT) These devices are indicated for resection of soft and osseous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Michigan recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.