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. 2,538 recalls have been distributed to Colorado in the last 12 months.
Showing 21701–21720 of 28,964 recalls
Recalled Item: MAKOplasty Hip Array Kit Laminate 150230 Recalled by Mako Surgical...
The Issue: Stryker Orthpaedics became aware that there is the potential for the 210540...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare PIIC Classic Upgrade Recalled by Philips Electronics...
The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare IntelliVue Info Center iX Recalled by Philips Electronics...
The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare IntelliVue Info Center iX Recalled by Philips Electronics...
The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) Recalled...
The Issue: The firm was notified by some of their customers that some of the sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wilson Penile Implantation System Retractor Frame Recalled by Abeon Medical...
The Issue: The firm was notified by some of their customers that some of the sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC...
The Issue: The firm was notified by some of their customers that some of the sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter Recalled by...
The Issue: Potential for separation of the proximal handle from the shaft.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System. Used to manage workflows for treatment...
The Issue: First Databank (FDB) is a third party product incorporated into MOSAIQ. FDB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hook Blade Recalled by Instratek, Incorporated Due to The sterile blade will...
The Issue: The sterile blade will not fit into the handle provided with the ETTD system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cournand Modified 2-PC 19G Recalled by Stryker Instruments Div. of Stryker...
The Issue: The Guidewire Introducer Needle (0910-192-000) was shipped after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...
The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ZYTO Tower is the input device to program the Recalled by ZYTO...
The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ZYTO Select and ZYTO Elite software programs are used Recalled by ZYTO...
The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...
The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 OUS Recalled by...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization...
The Issue: These screws have a single lead (instead of a triple lead) thread. The screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WARM STEAM Personal Steam Inhaler-Adjustable control to regulate flow of...
The Issue: "The public reason for the recall is that the product is being recalled out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aegis Torque Handle CATALOG NO. : 2871-10-800. A spinal surgical Recalled by...
The Issue: Manufacturing error within the Torque Handle may prohibit some handles from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve Recalled by Boston Scientific Corp...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.