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. 2,527 recalls have been distributed to Colorado in the last 12 months.
Showing 22541–22560 of 51,434 recalls
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 8 Fr 3 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 6 Fr 1.5 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ICS CHARTR EP 200 Recalled by GN Otometrics Due to There is a risk to...
The Issue: There is a risk to the healthcare professional or patient of exposure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229003A Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229000A Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568812910 Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229001A Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229037A Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sn-DMSA solution Recalled by Synthetopes Inc Due to Lack of Processing Controls.
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-d Recalled by Synthetopes Inc Due to Lack of Processing Controls.
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfur Colloid Reaction Vial 1.0 mL Recalled by Synthetopes Inc Due to Lack...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-Mertiatide Kit Recalled by Synthetopes Inc Due to Lack of Processing...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-Pyrophosphate Kit Recalled by Synthetopes Inc Due to Lack of Processing...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-Tetrofosmin Kit 5.0 mL Recalled by Synthetopes Inc Due to Lack of...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pentreotide (10 uGm) Recalled by Synthetopes Inc Due to Lack of Processing...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-DTPA Kit 10 mg Recalled by Synthetopes Inc Due to Lack of Processing...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...
The Issue: Multiple complaints were received for balloons bursting below the rated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Sheridan: 1) Uncuffed 6.0 mm Recalled by Teleflex Medical Due to...
The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT BNP Controls Ptoduct Usage: The ARCHITECT BNP Controls are...
The Issue: Presence of a time dependent, stability drift in patient and control results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.