Product Recalls in Colorado

Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,509 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,509 in last 12 months

Showing 2918129200 of 51,434 recalls

Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Spine Instrumentation Recalled by Medtronic Navigation, Inc. Due to...

The Issue: Potential for Spinal Clamps to be damaged when opened beyond intended...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Set Supplemental INS AxiEM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 29, 2017· Teva Pharmaceuticals USA

Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg 30 tablets per...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 29, 2017· Teva Pharmaceuticals USA

Recalled Item: Buprenorphine and Naloxone Sublingual Tablets Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 28, 2017· GSK Consumer Healthcare

Recalled Item: parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and...

The Issue: Presence of Foreign Substance: possibility of the presence of metal in the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 28, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: Obagi-C Rx System C-Therapy Night Cream Recalled by Valeant Pharmaceuticals...

The Issue: Labeling: Incorrect or Missing Package Insert - Obagi-C Rx System C-Therapy...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodJune 28, 2017· Kettle Foods, Inc.

Recalled Item: Kettle Brand Krinkle Cut Potato Chips Spicy Queso Recalled by Kettle Foods,...

The Issue: Carbohydrates on nutritional facts panel are stated as 3g/serving when the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 27, 2017· Peanut Butter holdings, LLC

Recalled Item: PB Crave Recalled by Peanut Butter holdings, LLC Due to Mislabeling

The Issue: Product mislabeled. "'Contains " allergen statement under the ingredient...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System Recalled by...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Cardinal Health 200, LLC

Recalled Item: Converters(R) Under Buttocks Drape with Fluid Control Pouch II Recalled by...

The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Cardinal Health 200, LLC

Recalled Item: Converters(R) Tiburon(R) Arthroscopy Drape Recalled by Cardinal Health 200,...

The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle Recalled...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety Deluxe Bone Marrow Biopsy/Aspiration Tray Recalled by Robert Busse &...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing