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. 2,120 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,120 in last 12 months

Showing 66216640 of 28,964 recalls

Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar breathing bag Set (P) 110 Recalled by Draeger Medical, Inc. Due to...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Circuit Kit Coax HEPA Recalled by Draeger Medical, Inc. Due to...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Basic (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Circuit Kit Coax 3 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist catheter is an intravascular micro axial...

The Issue: The Impella 5.5 pump experienced a heightened complaint rate for purge leaks.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Coax (P) 150 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Set Coax 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Ventstar Coax 180 Recalled by Draeger Medical, Inc. Due to Glued connections...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: ID Circuit Basic (P) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Watertrap (P) 180 w/oLL Recalled by Draeger Medical, Inc. Due to...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Set2Go Ventilation 12 (A) Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Ventstar Coax Recalled by Draeger Medical, Inc. Due to Glued connections of...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Bag Set (N) 110 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Basic (P)180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Ventstar Coax 230 Recalled by Draeger Medical, Inc. Due to Glued connections...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Anesthesia (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· DeRoyal Industries Inc

Recalled Item: Sterile custom surgical procedure packs: (1) 89-10507.02 Recalled by DeRoyal...

The Issue: The custom procedure packs contain light handle covers that have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products HbA1c Reagent Kit- IVD for the quantitative...

The Issue: Potential for both unexpected positive and negative HbA1c results, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Watertrap (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 14, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products Calibrator Kit 11 VANC Reagent Generation (GEN)...

The Issue: Unavailable to calibrate VITROS Chemistry Products VANC Reagent, Generation...

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

Class II — Potential Health HazardOngoing