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. 2,634 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,634 in last 12 months

Showing 1268112700 of 51,434 recalls

DrugMay 3, 2022· Apotex Corp.

Recalled Item: Sirolimus Oral Solution Recalled by Apotex Corp. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications: Sirolimus Oral Solution recalled due to...

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

Class III — Low RiskOngoing
Refund
FoodMay 3, 2022· Natural Organics, Inc.

Recalled Item: Keto Living Sugar Control Recalled by Natural Organics, Inc. Due to...

The Issue: Contains undeclared wheat (gluten) in product labeled "gluten free"

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 3, 2022· Canon Medical System, USA, INC.

Recalled Item: System: Alphenix 4D CT in combination with CAS-930A (C arm Recalled by Canon...

The Issue: CT operation may be restricted by an interlock which is a result of an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2022· Illumina, Inc.

Recalled Item: illumina Model NextSeq 550 Dx Recalled by Illumina, Inc. Due to...

The Issue: cybersecurity vulnerability

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2022· Illumina, Inc.

Recalled Item: illumina Model: MiSeq Dx illumina Model: Recalled by Illumina, Inc. Due to...

The Issue: cybersecurity vulnerability

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2022· Karl Storz Endoscopy

Recalled Item: STORZ KARL STORZ-ENDOSKOPE CMOS Video Cysto-Urethroscope Recalled by Karl...

The Issue: The endoscope may experience a loss of image when activating monopolar...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2022· Medtronic Xomed, Inc.

Recalled Item: NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version...

The Issue: Software anomaly was identified.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2022· Tornier, Inc

Recalled Item: Ratcheting Screwdriver Handle Recalled by Tornier, Inc Due to The device is...

The Issue: The device is unable to meet sterilization requirements when sterilized per...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2022· Medtronic Xomed, Inc.

Recalled Item: NIM Vital Console 4.0 (P/N: NIM4CM01) NIM with Software version 1.3.2...

The Issue: Software anomaly was identified.

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

Class II — Potential Health HazardOngoing
DrugMay 2, 2022· Amgen, Inc.

Recalled Item: MVASI (bevacizumab-awwb) Recalled by Amgen, Inc. Due to Defective container:...

The Issue: Defective container: loose crimp defect, potential loss of container integrity.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 1, 2022· The TJX Companies, Inc.

Recalled Item: Keats London Vegan Irish Cream Truffles in a 4.93-ounce round Recalled by...

The Issue: Product(s) may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2022· The TJX Companies, Inc.

Recalled Item: Keats London Vegan Hazelnut Dark Chocolate in a 4.93-ounce round Recalled by...

The Issue: Product(s) may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2022· The TJX Companies, Inc.

Recalled Item: Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.88-ounce green...

The Issue: Product(s) may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: buPROPion Hydrochloride Extended-Release Tablet Recalled by SUN...

The Issue: Presence Of Foreign Substance: Customer complaint for the presence of dark,...

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

Class III — Low RiskOngoing
Refund
DrugApril 29, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: buPROPion Hydrochloride Extended-Release Tablet Recalled by SUN...

The Issue: Presence Of Foreign Substance: Customer complaint for the presence of dark,...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 29, 2022· Nihon Kohden America Inc

Recalled Item: Adult Cap-ONE Biteblock The cap-ONE Biteblock is intended Recalled by Nihon...

The Issue: Due to products being shipped/distributed to customers after the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2022· Medtronic Xomed, Inc.

Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...

The Issue: The firm received reports of events related to airway obstruction while...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2022· Medtronic Xomed, Inc.

Recalled Item: NIM CONTACT EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to...

The Issue: The firm received reports of events related to airway obstruction while...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2022· Medtronic Xomed, Inc.

Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...

The Issue: The firm received reports of events related to airway obstruction while...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2022· Maquet Cardiovascular, LLC

Recalled Item: INTERGARD Woven Vascular Graft is a woven polyester graft coated Recalled by...

The Issue: Mislabeled: Product labeled as Intergard Woven Straight graft , D: 8 mm, L:...

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

Class II — Potential Health HazardOngoing