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. 2,696 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,696 in last 12 months

Showing 54215440 of 28,964 recalls

Medical DeviceOctober 11, 2023· Becton Dickinson & Company

Recalled Item: BD gravity sets (Product Name Recalled by Becton Dickinson & Company Due to...

The Issue: Affected infusion sets labeled as free of DEHP actually do contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Mc3 Inc

Recalled Item: NautilusTM ECMO Oxygenator with Balance Biosurface-used in extracorporeal...

The Issue: May have increased water path restriction within the heat exchanger, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Mc3 Inc

Recalled Item: NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal...

The Issue: May have increased water path restriction within the heat exchanger, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Unomedical A/S

Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...

The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Unomedical A/S

Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...

The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Medline manual resuscitators with integrated manometer Recalled by SunMed...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Curaplex manual resuscitators with integrated manometer Recalled by SunMed...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Becton Dickinson & Company

Recalled Item: BD Extension Sets (Product Name Recalled by Becton Dickinson & Company Due...

The Issue: Affected infusion sets labeled as free of DEHP actually do contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· SunMed Holdings, LLC

Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...

The Issue: A backwards leak present in the integrated manometer of the patient valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Becton Dickinson & Company

Recalled Item: BD Alaris Pump infusion sets (Product Name Recalled by Becton Dickinson &...

The Issue: Affected infusion sets labeled as free of DEHP actually do contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Randox Laboratories Ltd.

Recalled Item: RANDOX Total Bilirubin. Recalled by Randox Laboratories Ltd. Due to Randox...

The Issue: Randox has had reports of elevated patient results using Plasma (lithium...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2023· Unomedical A/S

Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...

The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2023· Maquet Medical Systems USA

Recalled Item: CARDIOHELP Emergency Drive Recalled by Maquet Medical Systems USA Due to...

The Issue: Product removal due to possible blocking or impairment of the CARDIOHELP...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 7600 Integrated System Product Code 6844461 Running Software...

The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...

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

Class II — Potential Health HazardOngoing