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 Feb 1, 2023

Parsley bunches Boxes of 30 and 60 count Keep refrigerated SKU 475987 PLU 4899 on twist ties Product of Mexico

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

Church Brothers, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 1, 2023

Getinge Flow-i Anesthesia Systems Flow-i C20, Part no. 6677200 Flow-i C30, Part no. 6677300 Flow-i C40, Part no. 6677400

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

Getinge USA Sales Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

Revogene SARS-CoV-2_IVD real-time RT-PCR test intended for the qualitative detection of RNA from SARSCoV-2 Catalog…

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

Meridian Bioscience Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

Air-Q3 AirQ3 Standard ILA with Manual Cuff Inflation and GA Size REF Number 0.0 50005 0.5 50055 1.0 50105 1.5 50155 2.0…

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

SunMed Holdings, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 1, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation

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

Teleflex LLC

2 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jan 25, 2023

Rasagiline Mesylate Tablets 1 mg; 30 tablets in HDPE bottle; Rx only; NDC 67877-260-30; Manufactured by Alkem…

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

Ascend Laboratories, LLC

FDA (openFDA drug enforcement)

Food

Reported Jan 25, 2023

Pasta Para Duris 12 oz. (340g) Brand Name: Melissa's UPC: 045255 152739 Distributed by: World Variety Produce, Inc. PO…

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

World Variety Produce Inc. dba Melissa's

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2023

BD Pyxis MedBank System - Product Label/labeling pending

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2023

Codman Surgical Patties, Part number 801400; SURG PATXRAY 1/2X1/2-200; Lot 6396457

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2023

Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400, Female Lock - Female Lock Guarded Luer Connector,…

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

International Medical Industries, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2023

Medline CISION Sterile Blades. Labeled as follows with corresponding Item Number. a. STERILE BLADE NO. 10 CARBON STEEL,…

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

MEDLINE INDUSTRIES, LP - Northfield

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2023

RadiaLux Lighted Retractor (Pink), REF: 50-101-1

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 18, 2023

True Goodness by Meijer Oat-Based Plain Yogurt Alternative, 24oz plastic tub, UPC: 7-13733-03918-5

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

Meijer Inc.

FDA (openFDA food enforcement)

Food

Reported Jan 18, 2023

Beijing Hawthorne Candy

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

Northern Food I/E Inc.

FDA (openFDA food enforcement)

Food

Reported Jan 18, 2023

PIETRZYK PIEROGI THE HOLY GOUDA PIEROGI, NET WT. 26.5oz (742g), 1 DOZEN UPC 850014236069

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

Pietrzyk Foods

FDA (openFDA food enforcement)

Medical devices

Reported Jan 18, 2023

VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…

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

Ventana Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 4, 2023

Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…

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

Acumed LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 4, 2023

Premium Quality Shirakiku Fish Sausage Original Net wt. 9.8 oz. (280g) UPC 074410366414 Ingredients: Fish meat (bream,…

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

Wismettac Asian Foods, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 4, 2023

XO Marshmallow Limited Edition: Banana Puddin' OMG (Ooey Marshmallow Goodness), 12oz. marshmallow fluff, 4 12oz. retail…

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

XO Marshmallow, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 28, 2022

InPen Diabetes Management App, part of the InPen System, REF: MMT-105ELBLNA, MMT-105ELGYNA, MMT-105ELPKNA,…

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

Companion Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2022

Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215

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

Corin Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2022

Centricity PACS-IW with Universal Viewer version 5.0. Used to display medical images (Including mammograms) and data…

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

GE Medical Systems, LLC

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2022

The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set…

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

Natus Medical Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2022

X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.

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

NuVasive 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.