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 48,122 notices were distributed nationwide, so they reach Michigan too — those are in the archive.

Medical devices

Reported Aug 26, 2015

Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine…

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

Siemens Medical Solutions USA, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2015

Bronchial Double Lumen Tube Set (Left), Sterile

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

Teleflex, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2015

2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Countersink Part #…

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

Trilliant Surgical Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2015

Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device…

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

Hitachi Medical Systems America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2015

Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare Way, Elyria, Ohio,…

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

Invacare Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 19, 2015

Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes…

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

Mason Vitamins, Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 12, 2015

***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp, Inc.***Dietary Supplement ***120…

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

MedOp Health, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 12, 2015

Merge Hemo, 9.10, 9.20.0, 9.20.1,9.20.2, 9.30, 9.40.0, 9.40.1, 9.40.2 with Massimo PHASEIN End Tidal CO2 (EtCO2)…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 12, 2015

Raw Frozen Tuna Chunks Product of Indonesia. The bulk frozen tuna products can be identified from the Purchase Order…

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

Osamu Corporation

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 12, 2015

Wish-Bone Ranch Dressing Net. Wt. 24 oz. Distributed by Pinnacle Foods Group USA LLC Cherry Hill, NJ 08003-3620 UPC…

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

Pinnacle Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 12, 2015

S2 Fluid Pack on the Cobas b 221 system- Catalog Number 03260925184 Blood Gas and Electrolytes Analyzer; The Roche…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2015

18inch Dual Port/Single Bladder Disposable Tourniquet Cuff, Zimmer Surgical, Inc. Tourniquets are intended to be used…

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

Zimmer Surgical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2015

Mission -Breath Alcohol Detector -15 tests - 0.08% BAC - Blow bags included Product Usage: The Breath Alcohol Detector…

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

Acon Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 5, 2015

Atkins Chocolate Candies  5 ct. cartons - UPC code 637480075558

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

Atkins Indiana Distribution Center

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 5, 2015

Fat Free Pasteurized Prepared Cheese Product: SOUTHHOME 12/12OZ AMERICAN FAT FREE YELLOW, 0788001319. ROUNDYS 12/12OZ…

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

Dairy Farmers OF America Inc.

33 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 5, 2015

Paragon Laboratory Management

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

McKesson Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2015

Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not freeze.

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

Musculoskeletal Transplant Foundation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2015

Invivo Expression MRI Patient Monitoring System.

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2015

Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence technology. Intended to produce cross-sectional…

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

Philips Medical Systems (Cleveland) Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2015

SYMMETRY SURGICAL DISPOSABLE TOWEL CLAMP, REF 19-4137, STERILE EO, Rx only. Apply clamps parallel to the skin with the…

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

Symmetry Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2015

Aequalis Humeral Nail Targeting Jig, Product Code: 9020060. Orthopedic manual surgical instrument.

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

Tornier, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

American Catheter / Cholangiogram Catheter 9100 Series.

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

American Catheter Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

Bausch & Lomb SofPort Advanced Optics Aspheric Lens

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

Bausch & Lomb Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 29, 2015

Polaris 4.75 TI Spinal System, 4.0 x 20 MM, Closed MAS, Closed Head Multiaxial Screw, Non-Sterile, Rx Only, REF…

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

Biomet Spine, LLC

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.