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.

4,634 stored notices name Michigan, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Michigan too — those are in the archive.

Medical devices

Reported Jan 28, 2026

Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version:…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers: ENDO-AN2030/B IN4130/CNK IN4130/H…

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

Merit Medical Systems, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog Number: HTHT0036 Software…

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

MicroPort Orthopedics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the…

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

Abbott Diabetes Care, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in…

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

Diagnostica Stago, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 21, 2026

Cinnamon, Clear Plastic Container, 100G, UPC 6251136 034139

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

Eureka Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 21, 2026

Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005.

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

Fresenius Kabi USA, LLC

FDA (openFDA device enforcement)

Food

Reported Jan 21, 2026

2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8

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

House Of Flavors, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 21, 2026

Pulsator Arterial Blood Sampling Kit, Item Numbers 4044EG-1 4080P-2 4084P-1 4080PE 4080PG

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

ICU Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.

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

Mobius Imaging, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag…

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

Thoratec LLC

FDA (openFDA device enforcement)

Food

Reported Jan 21, 2026

Troemner Family Farm Pfeffernusse Cookies, 6oz and 12oz bags

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

Troemner Farm

FDA (openFDA food enforcement)

Medical devices

Reported Jan 14, 2026

Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23

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

Applied Medical Resources Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2026

BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03,…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2026

Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when…

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

Integra LifeSciences Corp. (NeuroSciences)

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 14, 2026

Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly…

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

McCain Foods USA Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 14, 2026

Meijer Steam Distilled Water, 128 FL OZ (1 GAL) 3.78L, packaged in a plastic jug with red plastic lid, UPC…

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

Meijer Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 14, 2026

Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2026

The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with streptavidin-coated microparticles and…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 14, 2026

Town Food Service EQ CO Inc. brand Aluminum Sauce Pans in 1QT, 1.5QT, 2 QT, and 3QT sizes; UPC Codes: 843784003559,…

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

Town Food Service Equip Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 7, 2026

BVI Leos Laser and Endoscopy System. Model Number: OME6000U.

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

Beaver-Visitec International, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 7, 2026

Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201,…

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

Philips Ultrasound, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 31, 2025

BECKMAN COULTER BICARBONATE REF: OSR6137 OSR6237 OSR6637 OSR6x37 Bicarbonate is a system reagent for the quantitative…

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

Beckman Coulter Ireland, 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.