All recall categories

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.

Medical devices

Reported Sep 29, 2021

Access SARS CoV-2 IgG (1st IS) Assay: Access Immunoassay Systems REAGENT PACK, REF C74339 Access SARS-CoV-2 IgG (1st…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

Centricity PACS-IW with Universal Viewer - Product Usage: Is a device that displays medical images (including…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product Usage: is a general instrument intended…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

In2bones USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

DLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Perfusion Systems

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

EVIS EXERA BF-XT160 Bronchofibervideoscope, Model No. BF-XT160

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

Phantom Nail System, Drill, 4.6 x 300mm, Cannulated, 3/16" Sq. Connection p28 P99-110-4630

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Paragon 28, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: EPIQ 5 - 795120 EPIQ 5C - 795205…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System, Catalog Number 09211101190

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Roche Molecular Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 29, 2021

Kroger Kale Bag 16oz plastic bag 8 packages per case

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Kroger Co.

FDA (openFDA food enforcement)

Food

Reported Sep 22, 2021

Albanese World's Best Mini Gummi Butterflies 7.5oz UPC 634418523525

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Albanese Confectionery Group, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 22, 2021

Maxi Sky 1000 (Arjo) and V10 (BHM) Bariatric Ceiling Rail - Mounted Lift with measuring function

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arjohuntleigh Magog, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carefusion

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

Arjo Disposable Repositioning Sling, Model AHD001

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Getinge Dominican Republic SA

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

The Allura Xper series is intended for use on human patients to perform: "Vascular, cardiovascular and neurovascular…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

2 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 15, 2021

HAND SANITIZER (alcohol 80%), Alchol Antiseptic 80% topical solution, Hand Sanitizer non-sterile solution, Net weight…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Charles Paint Research Inc.

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 15, 2021

Proteus 235- designed to produce and deliver a proton beam for the treatment of patients with localized tumors and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ion Beam Applications S.A.

FDA (openFDA device enforcement)

Food

Reported Sep 15, 2021

Banoful Top Orange Biscuit

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Kbf Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 15, 2021

Pipeline Flex Embolization Device

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Micro Therapeutics Inc.,

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 8, 2021

BrightFarms Sunny Crunch; packaged in clear, plastic clamshells; 4oz and 8oz; grown at the company's Rochelle, Illinois…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bright Farms

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 8, 2021

TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DePuy Orthopaedics, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 8, 2021

Hostess Soft White Hamburger Buns, Net Wt. 12 OZ, UPC 888109110987

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hostess Brands, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 8, 2021

Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Magnolia Medical Technologies, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 8, 2021

Rocky Top Farms Cherry Butter sold in 1 gallon food service and 10oz retail sizes. 10 oz retail units may be sold…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Rocky Top Farm

FDA (openFDA food enforcement)

Medical devices

Reported Sep 8, 2021

Artis Models with SW version VD12 listed below: Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee MP…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

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.