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. 2,707 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,707 in last 12 months

Showing 36413660 of 28,964 recalls

Medical DeviceJune 27, 2024· Medivance Inc.

Recalled Item: Arctic Sun Temperature Management Systems Recalled by Medivance Inc. Due to...

The Issue: If temperature management system fails to reach correct target water...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· Boston Scientific Corporation

Recalled Item: Capio SLIM Suture Capturing Device Recalled by Boston Scientific Corporation...

The Issue: Some lots of Capio SLIM do not consistently catch the suture after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· Boston Scientific Corporation

Recalled Item: Capio SLIM Suture Capturing Device Recalled by Boston Scientific Corporation...

The Issue: Some lots of Capio SLIM do not consistently catch the suture after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· LINK BIO CORP

Recalled Item: LINK SymphoKnee Patella Sizing Template Recalled by LINK BIO CORP Due to The...

The Issue: The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2024· Siemens AG/Siemens Healthcare GmbH

Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...

The Issue: A potential issue with ARTIS icono systems equipped with a small detector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2024· Siemens AG/Siemens Healthcare GmbH

Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...

The Issue: A potential issue with ARTIS icono systems equipped with a small detector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2024· Siemens AG/Siemens Healthcare GmbH

Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...

The Issue: A potential issue with ARTIS icono systems equipped with a small detector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2024· UNIMAX MEDICAL SYSTEMS INC

Recalled Item: 1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch Recalled by...

The Issue: The tube may fall into the surgical site during the grasping process.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2024· Preat Corp

Recalled Item: Multiple Digital Analog Products labeled as: NobelBiocare...

The Issue: Due to a manufacturing issue, the product has a out of specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2024· Thoratec LLC

Recalled Item: HeartMate 3 System Controllers provided within the following HeartMate 3...

The Issue: Left ventricular assist system controller UI membrane/screen may lift along...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-2HH-6FH Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK MINI CR-2HH-1FH-P Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-12HH-1FH Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P Recalled by CareFusion 303, Inc. Due...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P Recalled by CareFusion 303, Inc. Due...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing