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.

Food

Reported Nov 17, 2021

Ingredion INSTANT PURE-FLO F (50 pound bag) food grade starch material 12151103CA

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

Ingredion Incorporated

FDA (openFDA food enforcement)

Food

Reported Nov 17, 2021

NOW Royal Jelly 1500mg 60 VCAPS UPC 733739025654 NOW Royal Jelly 1500mg 60 VCAPS (Distributed by Sofico) UPC…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

NOW Health Group Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 10, 2021

ImplantDirect, REF 834711, Legacy 2 Implant 4.7mmD x 11.5mmL, 4.5mmD Platform,

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

Implant Direct Sybron Manufacturing LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 10, 2021

Ivar's Kettle Classic Clam Chowder With Uncured Bacon, Item #1952, Costco Item #1270666. The soup is refrigerated and…

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

Ivar's Commissary

FDA (openFDA food enforcement)

Medical devices

Reported Nov 10, 2021

FIVE S 3.5x65, Flexible Intubation Videoscope, REF: 091361-01 (1 Unit), and 091361-06 (6 Units)

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Nov 10, 2021

IPL Coupling Gel, I L (AX1009013), 12 pack of 0.25 L (AX1009018), 6 pack of 1 L (AX1009019 or AX1009063); and IPL…

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

Lumenis, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 10, 2021

Fresh From Meijer, Honey Ham & Cheddar Pretzel Roll Sliders, 6.24 Oz., Plastic clam-shell - clear lid, black bottom,…

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

Meijer Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 10, 2021

Whole raw RED onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3…

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

ProSource Produce LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 3, 2021

Cliquid MD version 3.4 software used in conjunction with Analyst MD software on SCIEX Citrine & 4500MD series liquid…

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

Ab Sciex

FDA (openFDA device enforcement)

Food

Reported Nov 3, 2021

Nature's Heart Superfood Trail Mix 1.5oz poly film pouches - 32 units per case

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

Nestle USA Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 3, 2021

ASC PneumoLiner device, Part No. WA90500US (US market only) The Pneumoliner device is intended for use as a multiple…

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Food

Reported Nov 3, 2021

Simply Nature Organic Poppy Seed Dressing

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

Schlotterbeck & Foss LLC

FDA (openFDA food enforcement)

Food

Reported Nov 3, 2021

Almond Flour Crackers fine ground sea salt packaged in a white box with yellow graphics weighing 4.25 oz. Label reads…

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

Simple Mills

FDA (openFDA food enforcement)

Medical devices

Reported Nov 3, 2021

REF/Catalogue Number GSX0030A, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery…

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

W L Gore & Associates, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 27, 2021

SIMPLEXA COVID-19 Positive Control Pack, REF MOL4160, IVD, Rx Only, UDI: (01) 20816101027051

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

DiaSorin Molecular LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 27, 2021

Easi-Care Gait Belt Metal Buckle (54", 60", and 72" lengths)

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

Kinsman Enterprises Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 27, 2021

REF 8420.15.020, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=25mm, STERILE R, 2100099, UDI:…

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

Limacorporate S.p.A

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 27, 2021

Kit: Central Line Dres Change 20/Cs

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

Medical Action Industries, Inc. 306

FDA (openFDA device enforcement)

Medical devices

Reported Oct 27, 2021

VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls (IVD)- For use in monitoring the performance…

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

Ortho Clinical Diagnostics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 27, 2021

EPIQ CVxi Diagnostic Ultrasound Systems, Product Code: 795232

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

Philips Ultrasound Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 27, 2021

Tenaculum, Plastic

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

Stradis Medical, LLC dba Stradis Healthcare

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 20, 2021

Tone s Taco Seasoning Blend, Plastic Bottles / 12 bottles per case with best by dates of SEPT 03 24 and SEPT 06 24, due…

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

B&G Foods North America, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 20, 2021

Power Processor 3K, 3K High Speed Stockyards Module Nameplate: PP 3K Stockyard (Refrig) 9707 REF A88116

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 20, 2021

BioPlex 2200 ANA Screen Control Set, REF: 663-1131 incompatible with ANA Screen Reagent Packs/ANA Kits, REF: 665-1150;…

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

Bio-Rad Laboratories, 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.