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 Nov 25, 2020
1. Giant brand " Premium Apple Cider*** 64 fl. oz. (Half Gal) 1.89L***Distributed by Foodhold USA LLC, Landover, MD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mayer Brothers Apple Products, Inc.
FDA (openFDA food enforcement)
Reported Nov 25, 2020
COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Elastic Traction Device, 11mm Lower. UPN: ER56041 Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro-Tech USA
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Trader Joe's brand Gluten Free Battered Halibut, SKU 00503822. Product of USA. Frozen product is packed in plastic bag…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Orca Bay Foods LLC
FDA (openFDA food enforcement)
Reported Nov 25, 2020
Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thomas Scientific
FDA (openFDA device enforcement)
Reported Nov 18, 2020
SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Product Usage: intended for use in the dermatologic and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesthetics Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Aldi Little Salad Bar Classis Coleslaw (Green cabbage and carrots), 14 oz. plastic bag UPC:0-414498-30217-7 Kroger…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Nov 18, 2020
EDI Novel Coronavirus COVID-19 IgG ELISA Kit, REF: KT-1032 Per label: This kit is intended for qualitative detection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epitope Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Strep B Carrot Broth One-Step, Ref. Z40, UDI: 00819398026499
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Nov 18, 2020
FRESH FROM MEIJER CANTALOUPE CHUNKS LARGE BOWL, 32oz Clear plastic container, UPC 219323109721. FRESH FROM MEIJER…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Meijer Inc./Traffic Dept.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 18, 2020
Niobe ES System, Models 001-006000-1 and 001-006100-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stereotaxis Inc.
FDA (openFDA device enforcement)
Reported Nov 11, 2020
Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Anesthesia System provides the functional feature…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 11, 2020
TroClose 1200 - Product Usage: intended for use in a variety of gynecologic, general and urologic endoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gordian Surgical
FDA (openFDA device enforcement)
Reported Nov 11, 2020
Ultra2 Resolution Variants System for Abnormal Hemoglobin Quantitation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Primus Corporation
FDA (openFDA device enforcement)
Reported Nov 11, 2020
Streamline MIS Navigation System Taps, Catalog numbers 04-CANNDRILL-MDN 04-CANNTAP-40-MDN 04-CANNTAP-45-MDN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 4, 2020
Revolution Apex, Revolution CT with Apex Edition, Model 5995000-5 - Product Usage: The system is intended for head,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 4, 2020
Eishindo brand "CUP JELLY (MINI); NET WT. 28.2oz (800g); 50pcs; INGREDIENTS: WATER, HIGH FRUCTOSE SYRUP, APPLE JUIC,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hadson (Toko) Trading Co., Inc.
FDA (openFDA food enforcement)
Reported Nov 4, 2020
Merge LIS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Nov 4, 2020
Happy Tot Superfoods Gluten Free Oat Bar Organic Blueberries & Oatmeal. SKU: TB-BLOT-5 and TB-BLOT-5-WM. Ready-to-eat…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nurture Inc. dba Happy Family
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 4, 2020
Streamline MIS Navigation System Taps, Catalog Nos. 04-CANNDRILL-MDN 04-CANNTAP-40-MDN 04-CANNTAP-45-MDN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 4, 2020
Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray System Model: 10848600 - Product Usage: he…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Bien-Air Surgery REF 1600407-001 SN **** FOOTCTRL OSSEODOC - Product Usage: intended to convert electrical energy to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bien-Air Surgery Sa
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 28, 2020
Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 mm) X 105 cm Expiration Date June 8th 2021 - July 22nd 2021…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Oct 28, 2020
NanoClave Connector; 1 unit per pouch, 100 multivac pouches per case;UDI (01)10887709051017(17)241201(30)100(10)4549051;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
98 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.