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. 2,609 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,609 in last 12 months

Showing 1684116860 of 28,964 recalls

Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R Recalled by...

The Issue: Potential breakage of the endoscope s insertion tube bending section during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno fiberscope URF-P6 Recalled by Olympus Corporation of the...

The Issue: Breakage of the endoscope's insertion tube bending section during surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno fiberscope URF-P6RP6 Recalled by Olympus Corporation of the...

The Issue: Breakage of the endoscope's insertion tube bending section during surgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Cook Inc.

Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a...

The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Hill-Rom, Inc.

Recalled Item: Progressa Bed - AC-powered adjustable hospital bed Recalled by Hill-Rom,...

The Issue: A component used within the braking system may break resulting in one or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Shimadzu Medical Systems

Recalled Item: Sonialvision Safire II Recalled by Shimadzu Medical Systems Due to When...

The Issue: When selecting serial radiography with a pulse rate of 7.5fps (including...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Beckman Coulter Inc.

Recalled Item: 1) Cytomics FC 500 With CXP Software BECKMAN COULTER 2) Recalled by Beckman...

The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 12, 2018· Beckman Coulter Inc.

Recalled Item: COULTER EPICS XL Flow Cytometer COULTER EPICS XL-MCL Flow Cytometer Recalled...

The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 12, 2018· Cook Inc.

Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000 US) G46022 is...

The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2018· Ellex iScience, Inc.

Recalled Item: ellex I.Science iTRACK 250A Recalled by Ellex iScience, Inc. Due to...

The Issue: Sterility failure found in one of the units in the lot.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2018· GE Medical Systems Information Technologies, Inc.

Recalled Item: GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The...

The Issue: CARESCAPE Central Station (CSCS) software version 2.0.2 units may experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 1 PDS PLUS Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2018· Riverpoint Medical, LLC

Recalled Item: RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style Recalled by Riverpoint...

The Issue: Product is labeled with "CE", but is not yet approved in the European Union.

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

Class III — Low RiskOngoing
Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux mini VIDAS System in combination with Quality Control VIDAS*...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*)...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper systems with Certeray X-ray Generator located in regions...

The Issue: There is an increase in the failure rate of certain Anode Drive Units (ADU5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· Toshiba American Medical Systems Inc

Recalled Item: Diagnostic Ultrasound System Recalled by Toshiba American Medical Systems...

The Issue: The power supply unit may be damaged and may fail to start up when the power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Radiology CT with 4.2.0 software version. Model Recalled...

The Issue: Software issues including: Software errors that may result in Extended Field...

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

Class II — Potential Health HazardOngoing