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. 2,563 recalls have been distributed to Colorado in the last 12 months.
Showing 19201–19220 of 28,964 recalls
Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X upgraded to XCT 882454 Recalled by Philips Medical Systems...
The Issue: The intended use listed in the English and localized language IFUs for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: The intended use listed in the English and localized language IFUs for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction Chest Drain Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Express Dry Seal Suction OCEAN DRAIN Recalled by Atrium Medical...
The Issue: Chest drains manual vent valve located at the top of affected chest drains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keyspan High-High Speed USB to Serial Adapter Product Usage: The Recalled by...
The Issue: Power outages causes reporting software to shutdown.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAKO RIO THA Application User Guides Recalled by Mako Surgical Corporation...
The Issue: Five (5) AFMEA Risk Control Measures are missing from the MAKO RIO THA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX Cardiovascular The IMPAX CV Reporting module consists of a Recalled by...
The Issue: A customer experienced when using IMPAX CV Reporting software, specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Program Update Package AutoDELFIA¿ 3.0 Recalled by PerkinElmer Health...
The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Recalled by Siemens Healthcare Diagnostics,...
The Issue: Negative bias with IMMULITE¿ /IMMULITE¿ 1000 Third Generation PSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008K@home Series : Hemodialysis System Recalled by Fresenius...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Product Usage: Used to make treatment plans Recalled by...
The Issue: Incorrect Enhanced Dynamic Wedge (EDW) or Virtual Wedge (VW) Calculations.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELFIA¿ PC with V3.0 Software Recalled by PerkinElmer Health Sciences, Inc....
The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008K2 Series : Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoDELFIA¿ Plate Processor Recalled by PerkinElmer Health Sciences, Inc....
The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T Series Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Recalled by Siemens Healthcare Diagnostics,...
The Issue: Negative bias results with the IMMULITE¿ /IMMULITE¿ 1000 Third Generation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008K Series : Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.