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. 1,119 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,119 in last 12 months

Showing 14841–14860 of 28,964 recalls

Medical DeviceDecember 19, 2018· XTANT MEDICAL INC

Recalled Item: Calix Lumbar Spinal Implant System: 22mm x 10mm x 7mm PLIF ASSY PC Recalled...

The Issue: This recall has been initiated due to a change in packaging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Reckitt Benckiser LLC

Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...

The Issue: Five batches of the product have failed the specification of 1.0kPa for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Cook Inc.

Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...

The Issue: There is a potential for difficulty in sliding down the retention mechanism...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2018· Associates of Cape Cod, Inc.

Recalled Item: Fungitell Kit Recalled by Associates of Cape Cod, Inc. Due to The kits may...

The Issue: The kits may contain the incorrect number of components or the kits may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: "J" Type Bone Marrow Needle 11ga x 10 cm - Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Double Diamond J Type Bone Marrow Needle & Marrow Extraction Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja para Biopsia Tipo Medula Osea Ergonomica 11ga x 10cm Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: J Type Bone Marrow Needle 13ga x 6cm - Product Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Insulet Corporation

Recalled Item: Omnipod DASH Insulin Management System Recalled by Insulet Corporation Due...

The Issue: There is a potential for a communication interruption following a bolus...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja de Aspiration con Profundidad Ajustable Tipo I 15ga x Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: J Type Bone Marrow Needle 13ga x 10 cm- Product Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Anti-HAV IgM test System Recalled by Roche Diagnostics Corporation Due to...

The Issue: Potential for erroneous result messages for the Anti-HAV IgM assay when run...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Tina-quant IgM Gen.2 Recalled by Roche Diagnostics Corporation Due to New...

The Issue: New endogenous interference claims have been established for the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Lactate Gen.2 Recalled by Roche Diagnostics Corporation Due to New...

The Issue: New endogenous interference claims have been established for the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus TJF-Q180V Duodenoscope - Product Usage: These endoscopes are...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus PCF-Q180AC Video Colonoscope - Product Usage: These endoscopes are...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus GIF-H180J Gastrointestinal Videoscope - Product Usage: These...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing