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 Dec 10, 2025

Reagent Kits/ containing flow cells, components of NextSeq 550Dx Instrument: NextSeq 550Dx High Output Reagent Kit v2.5…

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

Illumina, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 10, 2025

Loaded Veggie Grain Bowl; NET WT. 10/90 OZ (309g) NO UPC Identifying N4L code: V3FR

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

Nutrition for Longevity

FDA (openFDA food enforcement)

Medical devices

Reported Dec 10, 2025

Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,

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

Philips Ultrasound, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 10, 2025

Lava Bun with Green Tea Flavor bright lime green packaging (Frozen) Unsalted butter and cream are listed in the…

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

Prime Food Processing LLC.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 10, 2025

Italian Salad Dressing; Net 1 GAL (3.78L) SKU: 7 67367 00518 4 Creamy Poblano Avocado Ranch Dressing and Dip; Net…

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

Ventura Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/…

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

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated…

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

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02

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

Djo, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

FlexLab (FLX); Version: FLX-217-10;

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

Inpeco S.A.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

CareLink Clinic, REF: MMT-7350

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450

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

Remel, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

MONARCH Bronchoscope. Model Number: MBR-000211-B

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

Auris Health, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60, IVD in conjunction with a Honeywell Vuquest…

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

Cellavision AB

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Clot Activator Model/Catalog Number: 455071P Product…

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A,…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 26, 2025

Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches

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

Plenus Group Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 26, 2025

OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult…

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

Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US,…

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

Thoratec LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 19, 2025

VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow PRUTest is a whole blood…

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

Accriva Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 19, 2025

CEREPAK Detachable Coil System - Name/REF: UNIFORM 2MM X 2.5 CM/FCX100202, UNIFORM 2.5MM X 3.3 CM/FCX100253, UNIFORM…

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

Cerenovus Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 19, 2025

Loaded Veggie Grain Bowl; Net Wt. 10.90 Oz (309g) GTIN code: 00818905028162

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

FreshRealm

FDA (openFDA food enforcement)

Food

Reported Nov 19, 2025

Peach Salsa; UPC 85006540364 14oz (397g); Use by 10/12/2025 to 10/29/2025

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

GBC Food Services, LLC

FDA (openFDA food enforcement)

Food

Reported Nov 19, 2025

Peach Salsa - $5.99-16 oz 639123940636 packaged in clear plastic clamshells Sell by 11/3/2025 Sell by 11/4/2025

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

Jfe Franchising Inc.

FDA (openFDA food 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.