Product Recalls in Vermont
Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,541 recalls have been distributed to Vermont in the last 12 months.
Showing 2301–2320 of 27,157 recalls
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: 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: 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: 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: 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: 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 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 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: 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: 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: 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: 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: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to faulty circuit board in speed control remote use in conjunction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to faulty circuit board in speed control remote use in conjunction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLENE Polypropylene Suture Recalled by Ethicon, LLC Due to Sutures may...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL Polyester Suture Recalled by Ethicon, LLC Due to Sutures may...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERMA-HAND Silk Suture Recalled by Ethicon, LLC Due to Sutures may have an...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Delivery System 10mmx10mm UPN: M00553740 Recalled by Boston...
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: HOT 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.