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. 2,551 recalls have been distributed to Colorado in the last 12 months.
Showing 19901–19920 of 51,434 recalls
Recalled Item: Uroskop Omnia max Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens became aware of an issue of incorrect use of the bypass key...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dutasteride Capsules Recalled by AVKARE Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Garlic Parmesan Sauce Recalled by Golden State Foods Due to Notification by...
The Issue: Notification by supplier of a recall of starch ingredient due to metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taco Bell Creamy Jalapeno Sauce Recalled by Golden State Foods Due to...
The Issue: Notification by supplier of a recall of starch ingredient due to metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pizza Hut Garlic Dipping Sauce Recalled by Golden State Foods Due to...
The Issue: Notification by supplier of a recall of starch ingredient due to metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Colonel's Coleslaw Dressing Recalled by Golden State Foods Due to...
The Issue: Notification by supplier of a recall of starch ingredient due to metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only Recalled by...
The Issue: Sterile drapes packaged in an unsealed pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally Recalled...
The Issue: Sterile drapes packaged in an unsealed pouch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex ProVent Arterial Blood Sampling Kit with Dry Lithium Heparin Recalled...
The Issue: Lots of Smiths Medical Portex Pro-Vent and LineDraw Arterial Blood Sampling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin...
The Issue: Portex Pro-Vent and LineDraw Arterial Blood Sampling syringes may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America BodyGuard Infusion Pump System Recalled by CME America, LLC Due...
The Issue: Infusion Pump Systems may have a delivery inaccuracy of up to 13%, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...
The Issue: Potential for thermal damage near the power cord connector and Power Entry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...
The Issue: Potential for thermal damage near the power cord connector and Power Entry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Humidity Pack (Qty 5) Recalled by Siemens Healthcare...
The Issue: A software error is causing the analyzer to incorrectly eject affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Humidity Pack (Qty 1) Recalled by Siemens Healthcare...
The Issue: A software error is causing the analyzer to incorrectly eject affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Brain 3.0 Application-Brain Recalled by MEDTECH SAS Due to Some...
The Issue: Some cross-sectional images from the image acquisitions of the patients head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA One 3.1 Brain Application Recalled by MEDTECH SAS Due to Some...
The Issue: Some cross-sectional images from the image acquisitions of the patients head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.