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 Jun 12, 2013

Digitex Absorbable Polydiaxanone Suture, Size 2-0. Catalog Number / Code of product: 52031, 5203101400. The Digitex…

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

Coloplast Manufacturing US, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Biliary SES product is indicated for…

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

Cordis Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

Canister: CO2 canister with GE part numbers 1407-3200-000, 1407-7004-000, or M1084850. Intended to provide general…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is…

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

Maytex Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

REF 8229705 x1 NIM TriVantage EMG Endotracheal Tube 5.0 mm I.D. x 6.5 mm O.D. Medtronic Xomed, Inc., 6743 Southpoint…

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

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2013

BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

AngioDynamics Micro Introducer Kits under the following labeling: 1) AngioDynamics 4F Standard Micro-Introducer Kit,…

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

Angiodynamics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2013

Heart Sync C100-Physio Radiotransparent Defibrillation Electrodes Monophasic or biphasic compatible pacing/…

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

Heart Sync, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2013

Meijer Diced Pears in Fruit Juice 8oz cup

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

Meijer Distribution, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 5, 2013

Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Plunger Delivery System, 4", Part…

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

Orthovita, Inc., dba Stryker Orthobiologics.

12 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2013

Peanut Butter Ribbon, 40 lb Pail, Item Numbers 07-012-40, 07-212-40, and 49-00100-40, Manufactured by Pecan Deluxe…

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

Pecan Deluxe Candy Company

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 5, 2013

***REF S-3D*** 3mm Diamond Ball. Used for cutting and shaping bone.

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

The Anspach Effort, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2013

next by Nature brand DARK CHOCOLATE BANANAS, NET WT. 3 Oz. (85g), UPC 8 17582 25600 4, Produced by Tropical Valley Foods

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

Tropical Valley Foods, Inc.

FDA (openFDA food enforcement)

Drugs

Reported May 29, 2013

Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg…

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

Aaron Industries Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported May 29, 2013

Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…

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

Alere San Diego, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

MyRay RXDC dental unit x-ray unit

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

Cefla Dental Group

FDA (openFDA device enforcement)

Food

Reported May 29, 2013

Krinos TAHINI ground sesame seeds, 1) Net. Wt. 1 lb (454g) in glass jars with gold lids packed 12 jars per case - UPC…

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

Krinos Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 29, 2013

Ref: VP1600 HD Still Capture System ConMed Linvatec . Captures, stores and transfers images generated by a medical…

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

Linvatec Corp. dba ConMed Linvatec

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Molift Smart 150

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

Moller Vital

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2013

Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Modified Coated…

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

Progressive Medical Inc.

16 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control System is used to treat urinary incontinence due to…

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

American Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innova 3100, Innova…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2013

Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)

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

Heartware 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.