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.
Reported Oct 7, 2020
365 Whole Foods Market Organic White Cheddar Popcorn, 4 oz. bag, UPC 099482428747, 16 retail units per wholesale case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eagle Family Foods Group LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 7, 2020
Pacific Xtreme (PTCA Balloon Dilation Catheter)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ev3 Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2020
Control, Calibrator Verified, Triage BNP, Model ALR88755
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2020
Speed Stitch Needle Cassette
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ArthroCare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2020
BECKMAN COULTER ACCESS Immunoassay Systems - Access Unconjugated Estriol, REF 33570.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2020
BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay, Treponema pallidum:UDI:03610520653012 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2020
NM/CT 850 Model Number: H3907AD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2020
Lightly salted microwave popcorn packaged in the following ways: 1) Cadia Organic Lightly Salted Popcorn, Net Wt. 9.9…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gilster-Mary Lee Corp.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 30, 2020
Inquiry Steerable Diagnostic Catheter, REF: IBI-81104 - Product Usage: INDICATIONS FOR USE The Inquiry fixed curve and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Irvine Biomedical Inc., a St. Jude Medical Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2020
The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v1.2 for 7500 RTPCR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2020
NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and communication system software that retrieves,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novarad Corporation
FDA (openFDA device enforcement)
Reported Sep 23, 2020
Peach Salsa, Keep Refrigerated packed in the following size containers and brands: 1. Crazy Fresh, Net Wt. 8 oz UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Russ Davis Wholesale, LLC
FDA (openFDA food enforcement)
Reported Sep 16, 2020
BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hellofresh US
FDA (openFDA food enforcement)
Reported Sep 16, 2020
SCHAWS SWEET AND SASSY GOURMET BARBECUE AND BASTING SAUCE, 18oz glass jar, UPC code 6 90379 81241
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lac O' Seasons Resort,Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 16, 2020
Merge PACS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2020
PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MicroPort Orthopedics Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
BD Alaris System. The EtCO2 module is a capnograph indicated for continuous, noninvasive monitoring of end tidal carbon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
Parvovirus B19 IgG EIA kit Part No. V519IGUS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diasorin Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
Symbia S-Series and Symbia T-Series - Product Usage: Intended use of the device SPECT: To detect or image the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stimwave Technologies Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2020
Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use of the system is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster (israel), Ltd.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Flexible Intubation Fiberscope, Part: 11301AA1, with Instruction Manual: Z18441US - Product Usage: are intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
7 more products in this recall
FDA (openFDA device enforcement)
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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.