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. 2,619 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,619 in last 12 months

Showing 1520115220 of 28,964 recalls

Medical DeviceSeptember 21, 2018· Becton Dickinson & Co.

Recalled Item: BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station Recalled by...

The Issue: The device may not function at the lower end (<15 deg. C) of the labeled...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 20, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Hybrid IABP Recalled by Maquet Datascope Corp - Cardiac Assist...

The Issue: There is a potential for interruption and/or inability to start therapy to...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Rescue IABP Recalled by Maquet Datascope Corp - Cardiac Assist...

The Issue: There is a potential for interruption and/or inability to start therapy to...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2018· Micro-Tech (Nanjing) Co., Ltd.

Recalled Item: Single-Use Biopsy Forceps Recalled by Micro-Tech (Nanjing) Co., Ltd. Due to...

The Issue: Single-Use Biopsy Forceps box contains incorrect product, instead it...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2018· AS Software, Inc.

Recalled Item: AS-OBGYN Information System version 7.824.x Recalled by AS Software, Inc....

The Issue: Any change made to current ultrasound machine software or hardware upgrades,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...

The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2018· Beckman Coulter Inc.

Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...

The Issue: Cross contamination may have occurred between wells for the reagent pack. As...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2018· COVIDIEN LLC

Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...

The Issue: Software Update: External USB Drive performance and its impact on Graphic...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic...

The Issue: O-arm 02 Imaging Systems correction to software version 4.1.0; new version...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· Leica Microsystems, Inc.

Recalled Item: BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301 Recalled by...

The Issue: The power supply unit for the printer used with the device can potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· BioMerieux SA

Recalled Item: NucliSENS¿ Magnetic Extraction Reagents Recalled by BioMerieux SA Due to...

The Issue: Data loggers showed that one shipment to the United States experienced low...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· Sterilmed, Inc.

Recalled Item: Reprocessed Agilis Steerable Introducer: indicated for introducing various...

The Issue: Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE LOGIQ E10 Ultrasound System Recalled by GE Healthcare, LLC Due to There...

The Issue: There is a potential for an undetected over temperature condition on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MC Recalled by GE Healthcare, LLC Due to A detector...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MG Multi-Geometry Digital CSE Dual Detector Gamma...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· Luminex Corporation

Recalled Item: VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as...

The Issue: Potential to lead to a false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled by...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing