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. 2,332 recalls have been distributed to Vermont in the last 12 months.
Showing 24081–24100 of 27,157 recalls
Recalled Item: Osseocare Pro Console & Set Osseocare Pro Recalled by Nobel Biocare Usa Llc...
The Issue: The recall was initiated because there is a potential for malfunction of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Brand Name(s): Alere Cholestech LDX¿ Lipid Profile"GLU Test Cassette...
The Issue: Alere initiated a recall of Cholestech LDX Lipid Profile-GLU test cassettes,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeiss brand IOLMaster Recalled by Carl Zeiss Meditec, Inc. Due to The user...
The Issue: The user database delivered for download contained an erroneous value....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable Recalled by...
The Issue: It was reported that the siderail may appear latched when it is not, due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeiss brand IOLMaster 500 Recalled by Carl Zeiss Meditec, Inc. Due to The...
The Issue: The user database delivered for download contained an erroneous value....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...
The Issue: The affected lots were exposed to a higher than acceptable level of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS brand ONCOR series Linear Accelerator Linac systems with component:...
The Issue: A safety risk regarding a potentially existing dark current radiation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...
The Issue: The affected lots were exposed to a higher than acceptable level of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS brand ARTISTE Linear Accelerator Linac systems with component: any...
The Issue: A safety risk regarding a potentially existing dark current radiation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT is a gamma camera for Single Photon Emission Recalled by...
The Issue: It was discovered the CT portion of the scan was interrupted ( stopping the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitreaCore¿ software. Versions subject to the limitation: 6.0 Recalled by...
The Issue: Vital Images, Inc. has found an issue in VitreaCore software though internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COUGAR¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zinger¿ Stainless Steel Workhorse Guidewire Recalled by Medtronic Vascular...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ Recalled by...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THUNDER¿ Extra Support Guidewire Recalled by Medtronic Vascular Due to...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZINGER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical's Inzii¿ 12/15mm Retrieval System. Applieds Inzii Tissue...
The Issue: Applied Medical is conducting a voluntary recall of the Inzii¿ 12/15mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTAIN HYBRID¿ Guide Wire Recalled by Medtronic Vascular Due to Potential...
The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prostiva RF Therapy Hand Piece Kit Recalled by Urologix, Inc. Due to A Hand...
The Issue: A Hand Piece high deployment force exceeded the maximum specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive has identified that the metalized coating on the IS3000 HD lamp...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.