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. 1,868 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,868 in last 12 months

Showing 3568135700 of 51,434 recalls

Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: The E.CAM gamma camera system Product Usage: The E.CAM gamma Recalled by...

The Issue: We received a customer complaint that Siemens reported via the MedWatch...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: system Recalled by Siemens Medical Solutions USA, Inc Due to In Artis zeego...

The Issue: In Artis zeego systems, angulations in the vicinity of the C-arm collision...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2016· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...

The Issue: The firm has received one report of values for patient height and weight...

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

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2016· Torrent Pharmaceuticals Limited

Recalled Item: Telmisartan Tablets Recalled by Torrent Pharmaceuticals Limited Due to...

The Issue: Presence of Foreign Substance: Product complaint for the presence of foreign...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 31" (79 cm) Appx. 3.4 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.6 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 110" (279 cm) Appx 13.8 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 74" (188cm) approximately 9.0ml Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2016· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...

The Issue: ICU Medical has identified an issue with a connection in an isolated number...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Purewick Corporation

Recalled Item: PureWick External Catheter for Women-Wick Product Usage: A flexible Recalled...

The Issue: PureWick is recalling external catheter for women Wicks because the labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ab Sciex

Recalled Item: Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the Recalled by Ab...

The Issue: Wrong quantitative results may be displayed in a report from the device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Air Walker Product Usage: Rebound Air Walkers are indicated Recalled...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Unloader Custom Lite Product Usage: Unloader Custom Lite is an Recalled by...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Cartilage Custom Product Usage: Rebound Cartilage Custom is an...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Papoose Infant Spine Immobilizer Item # Item Description: PA-100 Papoose...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Rebound Cartilage Product Usage: Rebound Cartilage is an external knee...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2016· Ossur H / F

Recalled Item: Knee Undersleeve Gray Product Usage: Knee undersleeves are worn as Recalled...

The Issue: Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve...

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

Class II — Potential Health HazardOngoing