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. 2,509 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,509 in last 12 months

Showing 2930129320 of 51,434 recalls

Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Cardioplegia Adapter with Pressure Port Provides access for a Recalled...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Pressure Monitoring Extension Line Adapters Extends the pressure line...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Extension Line Adapters 20 in length Used to extend Recalled by...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Pressure Disposable Pressure Display Sets Extends the pressure line...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
DrugJune 22, 2017· Advanced Pharma Inc.

Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2017· Advanced Pharma Inc.

Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2017· Advanced Pharma Inc.

Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2017· Advanced Pharma Inc.

Recalled Item: QUELICIN (Succinylcholine Chloride) Injection Recalled by Advanced Pharma...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2017· Lupin Pharmaceuticals Inc.

Recalled Item: Paroxetine Extended-Release Tablets USP Recalled by Lupin Pharmaceuticals...

The Issue: Failed Dissolution Specifications: out of specification observed in...

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

Class III — Low RiskOngoing
Refund
DrugJune 22, 2017· Vitility

Recalled Item: MAN OF STEEL capsules Recalled by Vitility Due to Undeclared Sildenafil

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 50mm Curved and precontoured Rod. Part of MAXIMIS Recalled...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Elekta, Inc.

Recalled Item: MOSAIQ(R) Oncology Information System Recalled by Elekta, Inc. Due to...

The Issue: Retention of Outdated Information in an Order Set. In the Care Plan Library,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Spinal & Epidural Anesthesia Tray. Product Catalog Number: 555172. Local...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix Continuous Epidural Anesthesia Tray. Product Catalog Numbers: 332075...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix Epidural AnesthesiaTray. Product Catalog Numbers: 551879 Recalled by...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: PENCAN Spinal Anesthesia Tray. Product Catalog Number: 560590. Local...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix Single Dose Epidural Anesthesia Tray. Product Catalog Number:...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix FX Epidural Anesthesia Tray. Product Catalog Numbers: 551993...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Customer Epidural Anesthesia Tray. Product Catalog Number: 555234. Local...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Pencan Spinal Needle Tray. Product Catalog Number: 333865. Local anesthesia...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing