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 2986129880 of 51,434 recalls

Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 100 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Solta Medical Inc

Recalled Item: VASER Amplifier Recalled by Solta Medical Inc Due to Potential inaccurate...

The Issue: Potential inaccurate calibration by service depot repair, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Solta Medical Inc

Recalled Item: VASER PRO Amplifier Recalled by Solta Medical Inc Due to Potential...

The Issue: Potential inaccurate calibration by service depot repair, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 2000 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 1000 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Product Usage: The da Vinci Recalled by...

The Issue: da Vinci Xi(R) Surgical System Patient Side Carts (PSC) were shipped to the...

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

Class II — Potential Health HazardOngoing
DrugMay 31, 2017· Teva Pharmaceuticals

Recalled Item: Paliperidone Extended-Release Tablets Recalled by Teva Pharmaceuticals Due...

The Issue: Failed Dissolution Specifications: Drug release test result, obtained during...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 31, 2017· Becton Dickinson & Company

Recalled Item: BD Precision Glide Needle 18G x 1 RB Recalled by Becton Dickinson & Company...

The Issue: Hub damage resulting in breakage and/or leakage during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2017· Encore Medical, Lp

Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...

The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2017· Encore Medical, Lp

Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...

The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...

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

Class II — Potential Health HazardOngoing
DrugMay 30, 2017· Mckesson Packaging Services

Recalled Item: BuPROPion HCL Tablets Recalled by Mckesson Packaging Services Due to Failed...

The Issue: Failed Moisture Limits: Product tested out-of-specification for moisture...

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2017· American Pharmaceutical Ingredients LLC

Recalled Item: Methocarbamol Recalled by American Pharmaceutical Ingredients LLC Due to...

The Issue: CGMP Deviations: Lack of quality assurance at the API manufacturer.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 26, 2017· Monfitello

Recalled Item: Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste NET...

The Issue: The firm was notified that the product may contain peanuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 26, 2017· Monfitello

Recalled Item: PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE Recalled...

The Issue: The firm was notified that the product may contain peanuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugMay 25, 2017· AstraZeneca Pharmaceuticals, LP

Recalled Item: BRILINTA (ticagrelor) tablets Recalled by AstraZeneca Pharmaceuticals, LP...

The Issue: Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 25, 2017· California Sun Dry Foods

Recalled Item: California Sun Dry Sun Dried Tomato Pesto Recalled by California Sun Dry...

The Issue: Firm employee noticed that incorrect back label was attached to Sun-Dried...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 25, 2017· Becton Dickinson & Company

Recalled Item: BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G...

The Issue: Product mislabel. Lot 6291768 of the BD Insulin Syringes with the BD...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Alcon Research, Ltd.

Recalled Item: LX3 Floor Stand for LuxOR Ophthalmic Microscope Recalled by Alcon Research,...

The Issue: Multiple shipments or forceful impact to a caster on a LuxOr/LX3 microscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Atrium Medical Corporation

Recalled Item: Atrium iCAST Balloon Expandable Covered Stent Recalled by Atrium Medical...

The Issue: Firm received a complaint that a customer who ordered an ADVANTA V12 7mm x...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01 Recalled by...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing