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 55415560 of 28,964 recalls

Medical DeviceSeptember 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPOINT 500e Blood Gas System Recalled by Siemens Healthcare Diagnostics...

The Issue: There are potential drug interferences from Perhexiline Maleate or...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: THERASPHERE ADMIN SET Recalled by B. Braun Medical, Inc. Due to Devices may...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: BULK LARGEBORE MALE LL FITTING Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPOINT 500 Blood Gas System Recalled by Siemens Healthcare Diagnostics...

The Issue: There are potential drug interferences from Perhexiline Maleate or...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: TERUMO 60" TUBE SET W/HIGH CRACK CHK VLV Recalled by B. Braun Medical, Inc....

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: 30 ML 2PORT BURETTE ASSEMBLY Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: AMO ADMINISTRATION SET Recalled by B. Braun Medical, Inc. Due to Devices may...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: 30ML BURETTE ASSY WITH STOPCOCK Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: ALLERGAN UNIVERSAL FILL KIT Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: FT1000S FLUID TRANSFER SET Recalled by B. Braun Medical, Inc. Due to Devices...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Transnasal esophagovideoscope-For endoscopy and endoscopic surgery within...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Gastrointestinal videoscope-indicated for use within the upper digestive...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Olympus Corporation of the Americas

Recalled Item: Insufflation unit Recalled by Olympus Corporation of the Americas Due to...

The Issue: Olympus has become aware of an increased trend of both repairs and customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Small intestinal videoscope-For endoscopy and endoscopic surgery within the...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Rhinolaryngoscope-for endoscopic diagnosis and treatment within the nasal...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Duodenovideoscope-EndoTherapy accessories (such as a biopsy forceps)...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Bronchoscope-for endoscopy and endoscopic surgery within the airways and...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Hysterofiberscope-For endoscopic diagnosis within the uterus. Model Number:...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Choleodochoscope. Model Numbers: CHF-BP30 Recalled by Aizu Olympus Co., Ltd....

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Gastroscope-endoscopic ultrasound (EUS) guided fine needle aspiration (FNA)...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing