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.

Food

Reported Jul 10, 2019

WOODSTOCK ORGANIC GRILLED RED PEPPER, NET WT 10. OZ, packaged in a plastic packaged marked with UPC Code: 4256301714.…

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

UNFI General Corporate

FDA (openFDA food enforcement)

Medical devices

Reported Jul 10, 2019

DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are…

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

Zimmer Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2019

LEEP Precision Integrated System 120V, Model LP-10-120 Product Usage: The LEEP PRECISION INTEGRATED SYSTEM l 20V…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2019

Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb…

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

Cytocell Ltd.

FDA (openFDA device enforcement)

Food

Reported Jun 26, 2019

30 Lbs IQF Wild Blueberries, Keep Frozen -10*C

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

Maine Wild Blueberry Company

FDA (openFDA food enforcement)

Food

Reported Jun 26, 2019

Maglio Companies Jalapeno Peppers sold in the following sized packages: 10 lb. Qdoba Pepper; 1-1/9 BU Pepper, Jalapeno…

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

The Fresh Group, Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 19, 2019

IntraClude Intra-Aortic Occlusion Device, REF: ICF100, 10.5 Fr (3.5 mm) X 39.4" (100 cm), Rx Only, Sterile EO The…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2019

Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote…

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

GE Healthcare, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2019

Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product Usage: Usage: The Getinge 86 Series…

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

Maquet Cardiovascular US Sales, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jun 19, 2019

Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by:…

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

Select Distributions LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 19, 2019

Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas Blender, Catalog #: 801188, UDI…

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

Terumo Cardiovascular Systems Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with…

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

Bio-Rad Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019,…

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

Microbiologics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

NxStage PureFlow B Solution, REF RFP-400, M535RFP4000 Product NxStage PureFlow B Solution is indicated for use with…

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

NxStage Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F

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

OriGen Biomedical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO…

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

Abbott MitraClip XTR Clip Delivery System, UDI: 08717648226366, Part: CDS0601-XTR, Sterile EO, Rx Only

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

Abbott Vascular

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

Horizon Cardiology Hemo

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

Change Healthcare Israel Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2019

Dole Classic Coleslaw (US) Shredded cabbage and carrots. 14 oz. US

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

Dole Fresh Vegetables

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 5, 2019

Fenestrated Taps 4.5mm, 5.5mm, 6.5mm (Ref#5001-90013, 5001-90014, 5001-90015) Product Usage: The K2M Fenestrated Tap…

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

K2M, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2019

Suja Organic Kombucha - Ginger Lemon: 15.2 oz. glass bottle; UPC 818617020232 DISTRIBUTED BY SUJA LIFE, LLC OCEANSIDE,…

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

Suja Life LLC

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 29, 2019

Deshi Golden Raisin, packaged in 3.5 oz, 7 oz. and 14 oz. clear plastic

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

Deshi Distributors, LLC

FDA (openFDA food enforcement)

Medical devices

Reported May 29, 2019

EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is used to optimize fluid…

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

Edwards Lifesciences, 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.