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Recalls distributed in Colorado

These notices name Colorado 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.

3,918 stored notices name Colorado, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Colorado too — those are in the archive.

Medical devices

Reported Jul 17, 2019

HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for…

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

Hamilton Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2019

ColoCARE, Cat. No. 5650, packaged 250 envelopes/box, For In-Vitro Diagnostic Use. The firm name on the label is Helena…

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

Helena Laboratories, Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 17, 2019

Revive Reusable Bladder Support, Model No. 0025 - Product Usage: The Revive bladder support is intended for temporary…

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

Rinovum Women's Health

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2019

ZOLL Pro-padz Liquid Gel Radiolucent, Part numbers: 8900-2105-01 (12/case) and 8900-2106-01 (single)

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

Bio-Detek, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 10, 2019

Signature Select Avocado Chunks, 12 oz. (340 g) Stand-up pouch Re-sealable, Keep Frozen; UPC 2113009412 Ingredient:…

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

Nature's Touch Frozen Foods (West)

FDA (openFDA food enforcement)

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 Jul 3, 2019

Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks, such as general purpose pipetting and…

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

Tecan US, 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)

Medical devices

Reported Jun 26, 2019

Cepheid Xpert C. difficile/Epi Control Panel

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

Microbiologics Inc.

FDA (openFDA device 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)

Food

Reported Jun 19, 2019

CHOCOLATE MILK CHOCOLATE MEIJI, 1.75 oz. Item number 70378 UPC 074410703783 - only on those bars with English labeling.…

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

Wismettac Asian Foods, Inc.

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 12, 2019

AngioDynamics Solero Microwave Tissue Ablation (MTA) System: Solero Generator PG (1) Catalog Number:12740000 UPN:…

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

Angiodynamics Inc. (Navilyst Medical Inc.)

4 more products in this recall

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

Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution

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

Kerr/Pentron, dba Kerr Corporation and Pentron Clinical

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

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)

Food

Reported Jun 5, 2019

purely elizabeth Coconut Cashew Grain-Free Granola, packaged in Net Wt. 8 oz. (227g) Re-sealable Pouch, UPC…

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

Oakhouse Bakery

9 more products in this recall

FDA (openFDA food 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)

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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.