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 Aug 12, 2026
Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contego Medical, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2026Updated Sep 16, 2026
Oribe Serene Scalp Densifying Shampoo, packaged in 8.5 fl. oz. (250 mL) bottles with UPC 840035231242 and 33.8 fl. oz.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.KAO USA Inc.
FDA (weekly enforcement report)
Reported Aug 12, 2026
Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Critical Care AB
FDA (openFDA device enforcement)
Reported Aug 12, 2026
Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pride Mobility Products Corp.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2026
Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree, 4oz/113g pouch, UPC 815367010780, PTO Item 10720.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PT Organics Limited
FDA (openFDA food enforcement)
Reported Aug 12, 2026
Brand Name: U2 Total Knee System Product Name: PSA Box Trial, L, #1-6 and PSA Box Trial, R, #1-6 Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.United Orthopedic Corp.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 7, 2026Updated Aug 25, 2026
Shan Distribution Network, Inc. Recalls Ineligible Frozen Siluriformes Breaded Fish Fillet and Stick Products Imported…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shan Distribution Network, Inc.
USDA FSIS
Reported Aug 5, 2026
L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Permobil Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ResMed Ltd.
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker GmbH
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2026
Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endoscopic Seal: GYN, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Jul 29, 2026
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Penumbra, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
3mensio Workstation (Vascular Fenestrated) software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PIE Medical Imaging B.V.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
FSIS Issues Public Health Alert for Steak Burrito Product Due to Misbranding and Undeclared Allergen
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Red's All Natural, Llc.
USDA FSIS
Reported Jul 29, 2026
SeaSpine Polyaxial Head REF Number: 41-3010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seaspine Orthopedics Corporation
FDA (openFDA device enforcement)
Reported Jul 22, 2026
Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amy's Kitchen Inc.
FDA (openFDA food enforcement)
Reported Jul 22, 2026
da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2026
Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2026
functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutricia North America
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 22, 2026
Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix U.S. LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2026
Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Jul 15, 2026
Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, 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.