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. 2,684 recalls have been distributed to Colorado in the last 12 months.
Showing 7641–7660 of 28,964 recalls
Recalled Item: Prismaflex M Set: M150 (product code 109990). For use in Recalled by Baxter...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex HF Set: HF1000 (product code 107140) Recalled by Baxter...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoTHOR Gen 2.5 Regular whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoTHOR Gen 2.0 whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G041 POD Recalled by Thor Photomedicine Ltd Due to Failure of ball stud...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoTHOR Gen 2.5 XL whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADLT BLOOD CLUTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE PHERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756 Recalled by MEDLINE...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE BLOOD CLUTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE 24 BLOOD CLUTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR Recalled by...
The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product/Part: MitraClip NTR Clip Delivery System US/CDS0601-NTR Recalled by...
The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product/Part: MitraClip G4 CDS NT REPAIR-MR Clinical/CDS0704-NT Recalled by...
The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter Recalled by...
The Issue: Manufacturing error resulted in potential contamination of Bi-Directional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTURION SnagFree Chest Tube insertion Tray Recalled by MEDLINE INDUSTRIES,...
The Issue: One lot of chest tube insertion trays, containing a silk suture component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima Coil System Model Number OPTI0208CSS10 Recalled by BALT USA, LLC Due...
The Issue: Product pouch label does not match up with carton label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wisp and Wisp Youth Nasal Mask Recalled by Philips Respironics, Inc. Due to...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DreamWisp Nasal Mask with Over the Nose Cushion Recalled by Philips...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics Amara View Minimal Contact Full-Face Mask Recalled by...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.