All recall categories

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.

3,911 stored notices name Colorado, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Colorado too — those are in the archive.

Medical devices

Reported Oct 14, 2026Updated Oct 20, 2026

Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model…

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

Philips Medical Systems

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2026Updated Oct 20, 2026

SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;

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

Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2026Updated Oct 20, 2026

Battle Bandage, REF: 32-700; Patrol IFAK Bag, Black - Advanced, REF: 81-125-BL; Patrol IFAK Bag, Multicam - Advanced,…

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

Safeguard US Operating LLC

FDA (openFDA device enforcement)

Food

Reported Oct 14, 2026

SIERRA NEVADA GRAZIERS RAW MONTEREY JACK NET WT. 8oz. (225g) ITEM 6400 Plant No. 06-325 Willows, California 95988 UPC:…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Sierra Nevada Cheese Company, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001; Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part:…

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

Alere San Diego, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 18) WHITE Model/Catalog Number:…

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

ASP Global, LLC.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a…

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

Draeger, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

HeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI…

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

Brand Name: Penumbra System (RED 62 Reperfusion Catheter) Product Name: Penumbra System (RED 62 Reperfusion Catheter)…

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

Penumbra Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

In-Line Valve, Product Number: P5-TEE

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

Percussionaire Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

Computed Tomography X-ray System, Model: uCT 530 with software

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

Shanghai United Imaging Healthcare Co., Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

CHARLOTTE CLAW Screw, REF: 40122716, intended for use with CLAW II Polyaxial Compression Plating System

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

Wright Medical Technology, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Oct 2, 2026Updated Oct 25, 2026

Inexport Logistics LLC Recalls Ineligible Pork Cracklings Products Imported From The Republic of Colombia

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

Inexport Logistics LLC

USDA FSIS

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Brand Name: VOLARA System Product Name: VOLARA, HC, NA A Model/Catalog Number: M08594A Software Version: N/A Product…

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

Baxter Healthcare Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter…

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

Becton, Dickinson and Company

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US, CAT 8100E1-US, CAT 8100EP1, CAT 8100EP1-ST, CAT…

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

Criticare Technologies, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

GreenTripe.com Frozen Dog Food Xkaliber Net Wt. 1 lbs (453g). Packaged in rolls, 36 rolls per case. GreenTripe.com…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

GreenTripe.com,Inc.

FDA (weekly enforcement report)

Drugs

Reported Sep 30, 2026Updated Oct 7, 2026

Cornea

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

Rocky Mountain Lions Eye Bank

FDA (weekly enforcement report)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached Gimbal, 12mm REF: MD1-300010-12

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

Seaspine Orthopedics Corporation

FDA (openFDA device enforcement)

Food

Reported Sep 30, 2026Updated Oct 7, 2026

Reese's Crunchy Peanut Ice Cream Bar, 2.0 fl. oz. ice cream bars, paper cartons containing individually wrapped ice…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Unilever North America Supply Chain Company, LLC

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…

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

Bard Access Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1)…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101…

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

Happiest Baby, Inc.

1 more product in this recall

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.