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 48,124 notices were distributed nationwide, so they reach Michigan too — those are in the archive.
Reported Sep 5, 2012
Markets of Meijer, fresh Grillers, Mushrooms with Rosemary, 10 oz, Ingredients: Mushrooms, Rosemary, Product of Canada,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pure Hothouse Foods Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 5, 2012
Siemens Stratus(R) CS Acute Care(TM) D-dimer Calibrator (DDM CalPak) lots 502058002 and 501318002 The Stratus(R) CS…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Sep 5, 2012
Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessory Packs (also commonly known as convenience…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SRI Surgical
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Hitachi Echelon MRI System/Oasis MRI, Software. These are software controlled MRI devices. Product Usage: The Echelon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Medtronic O-arm¿ Imaging System. Product Numbers: BI-700-00027-100, BI-700-00027-100R, BI-700-00027-120,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Menno Beachy, Cresco, IA Certified Organic Grape Tomato packaged in 1-pint square-shaped clear plastic clamshell…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Menno Beachy
FDA (openFDA food enforcement)
Reported Aug 29, 2012
syngo Dynamics Version 9.5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions, USA, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Spartan/Fresh Selections Wedge Sandwich W/Sandwich Spread 4oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spartan Central Kitchen
FDA (openFDA food enforcement)
Reported Aug 29, 2012
Serial interface module RS-232 Product Usage: The System 1 provides perfusion case data transfer through the use of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2012
DePuy Custom Implant Devices Packaging: Packaging was not standardized on customs, it was dependant on the geometry of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Aug 22, 2012
FunFresh Foods World Berry Organic Cacao Nibs 6 oz, packaged in blue, brown, red, white, black and green packaging with…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.FunFresh Foods Inc.
FDA (openFDA food enforcement)
Reported Aug 22, 2012
GE Healthcare Advantage Workstations, Advantage Worksation version 4.2 and 4.3 with Volume Viewer 2 (version 6.4-6.8)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 22, 2012
Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt Germany Phone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Inc.
FDA (openFDA device enforcement)
Reported Aug 22, 2012
13.5 mm x 50 mm BrainPath Sheath The NICO BrainPath is a family of products that consists of multiple sized reusable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nico Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2012
Synthes(R) Hemostatic Bone Putty, Part numbers 08.901.001.97S, 08.901.001.98S, 08.901.001.99S, 08.901.001D, and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Synthes USA HQ, Inc.
FDA (openFDA device enforcement)
Reported Aug 22, 2012
TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
FDA (openFDA device enforcement)
Reported Aug 15, 2012
The finger cots are made out of natural rubber. They are disposable products used to cover a fingertip bandage when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Afassco Inc.
FDA (openFDA device enforcement)
Reported Aug 15, 2012
Chromovision High Definition (HD) Wireless Camera, Pt # CC-9715900. Visual recording of surgical procedures.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Berchtold Corp.
FDA (openFDA device enforcement)
Reported Aug 15, 2012
Philips MultiDiagnost Eleva with Flat Detector (MD Eleva FD)Model: 708034 Product Usage: Philips X-ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare Inc.
FDA (openFDA device enforcement)
Reported Aug 15, 2012
The ABL software version 6.12 for the ABL800 analyzer. The analyzers are intended for the in Vitro testing of: -Samples…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Major brand Infants' Mapap, Acetaminophen Concentrated Drops, 1 FL. OZ. (30 mL.) 80 mg. per 0.8 mL, Cherry Flavor,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Axcentria Pharmaceuticals LLC
FDA (openFDA drug enforcement)
Reported Aug 8, 2012
Defense Nutrition Warrior Whey Natural Powder, dietary supplement, packaged in 14-oz. bottles and packed 6/14-oz…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Defense Nutrition
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 8, 2012
Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total Shoulder Arthroplasty
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2012
Integra¿ Advansys Medial Lisfranc Plate (MLP), Integra, 311 Enterprise Drive, Plainsboro, NJ 08536 The Advansys plates…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
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.