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. 2,596 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,596 in last 12 months

Showing 1766117680 of 28,964 recalls

Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Curved Suction 70 9733450 EM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Straight Suction 9733449 EM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Sorin Group USA, Inc.

Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...

The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Boston Scientific Corporation

Recalled Item: EMBLEM MRI S-ICD Model 219 Recalled by Boston Scientific Corporation Due to...

The Issue: The device can deliver an atypical amount of energy due to memory corruption...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Boston Scientific Corporation

Recalled Item: SQ-RX 1010 Pulse Generator Recalled by Boston Scientific Corporation Due to...

The Issue: The device can deliver an atypical amount of energy due to memory corruption...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Roche Diagnostics Corporation

Recalled Item: Brand Name: ¿ cobas c 6000 MODULAR Series System e Recalled by Roche...

The Issue: Roche has confirmed that a possible sample mismatch issue may occur on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety Deluxe Bone Marrow Biopsy/Aspiration Tray Recalled by Robert Busse &...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System Recalled by...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· NOVADAQ TECHNOLOGIES INC.

Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...

The Issue: The sterile drape material may contain a pinhole compromising its integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle Recalled...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Laceration Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse Hospital...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle...

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables

Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....

The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2017· Hologic, Inc

Recalled Item: Tomcat Instrument Recalled by Hologic, Inc Due to A Tomcat Instrument...

The Issue: A Tomcat Instrument software anomaly that causes the pipettor arm to make...

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

Class II — Potential Health HazardOngoing