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. 1,165 recalls have been distributed to Colorado in the last 12 months.
Showing 2361–2380 of 28,964 recalls
Recalled Item: Brand Name: SenTiva DUO" Product Name: VNS Therapy¿ SenTiva DUO" Recalled by...
The Issue: Their is a potential that implanted pulse generators may stop delivering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Socrates 38 Aspiration Catheter 127 cm length The Recalled by Scientia...
The Issue: Due to manufacturing non-conformance that resulted in channels in the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Recalled...
The Issue: Disposable set may leak during priming from a female quick connector due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access PCT Reagent Pack Recalled by Beckman Coulter Inc. Due to Identified...
The Issue: Identified reagent lots are experiencing a high rate of calibration failures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK...
The Issue: Due to devices being irradiated above the established specification which my...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alteon XLE Item Number / Product Description: 140-22-70 NV EHXL Recalled by...
The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY Recalled by MEDLINE...
The Issue: The catheter subassembly in the Integrated Arterial Catheter was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline General Surgery Tray Kits: 1) ARTERIAL LINE INSERTION KIT Recalled...
The Issue: The catheter subassembly in the Integrated Arterial Catheter was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation XLE Item Number / Product Description: 140-22-70 NV EHXL Recalled...
The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AcuMatch XLE Item Number / Product Description: 140-28-27 AM EHXL Recalled...
The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeiMed NasoGel for DRY NOSES UDI-DI/code: 00705928045309 SKU...
The Issue: Due to nasal spray stability failure for bioburden.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Guard Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Recalled by Hollister Incorporated Due to Hollister received...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VDR4 Phasitron Breathing Circuit Models that contain the venturi component:...
The Issue: Due to internal venturi component getting transiently stuck in the forward...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast SlimFit Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Guard Select Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Treatment Delivery System Recalled by Accuray Incorporated Due to...
The Issue: Snap rings may become partially or completed detached from the shafts within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Continu-Flo Solution Set with Duo-Vent Spike Recalled by Baxter...
The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.