Product Recalls in Virginia

Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,921 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,921 in last 12 months

Showing 2614126160 of 29,425 recalls

Medical DeviceOctober 23, 2013· Stryker Medical Division of Stryker Corporation

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Carl Zeiss Meditec, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Siemens Medical Solutions USA, Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Siemens Medical Solutions USA, Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Alere San Diego, Inc.

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.

Class III — Low RiskOngoing
Medical DeviceOctober 23, 2013· Philips Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

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.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

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.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

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.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Urologix, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: THUNDER¿ 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.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ProVia¿ CROSSING 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.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

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.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

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.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Applied Medical Resources Corp

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Intuitive Surgical, Inc.

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.

Class III — Low RiskOngoing
Medical DeviceOctober 21, 2013· Vital Images, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

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.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 18, 2013· Intra Pump Infusion Systems

Recalled Item: CRN Crono Syringe CRN20 with 19G x 1 "Steel Needle" Recalled by Intra Pump...

The Issue: Product has the potential to have a clear debris on the tip of the needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2013· SpineFrontier, Inc.

Recalled Item: PedFuse Reset Screw Recalled by SpineFrontier, Inc. Due to During routine...

The Issue: During routine servicing, it was discovered that one 8mmx55mm Reset screw...

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

Class II — Potential Health HazardOngoing