Product Recalls in Nevada

Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,510 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,510 in last 12 months

Showing 2572125740 of 28,334 recalls

Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SST Bifurcated Grafts >or= 6mm Intended for use in Recalled by...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VXT Grafts <6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta VS Grafts >or= 6mm Intended for use in arterial vascular...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Advanta SST Grafts >or= 6mm Intended for use in arterial Recalled by Atrium...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Flixene Grafts >or= 6mm Intended for use in arterial vascular reconstruction...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Atrium Medical Corporation

Recalled Item: Flixene IFG Vascular Grafts >or= 6mm Intended for use in Recalled by Atrium...

The Issue: Inner tray label may adhere to wall of outer tray which make it difficult to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Stryker Medical Division of Stryker Corporation

Recalled Item: IsoGel AIR 84 Recalled by Stryker Medical Division of Stryker Corporation...

The Issue: Complaints were received from the field indicating that some Air Pumps were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2013· Celera Corporation

Recalled Item: OLA Buffer For Laboratory Use Recalled by Celera Corporation Due to The...

The Issue: The package insert for FG OLA Buffer, GPR displayed the wrong concentration...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2013· DePuy Orthopaedics, Inc.

Recalled Item: LPS Lower Extremity Dovetail Intercalary component. Intended for use in...

The Issue: The LPS Lower Extremity Dovetail Intercalary component has the potential for...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2013· Cayenne Medical Inc.

Recalled Item: AperFix AM Femoral Implant Recalled by Cayenne Medical Inc. Due to Potential...

The Issue: Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Acuson SC2000 volume imaging ultrasound systems at software version 3.0....

The Issue: Software issue results in inaccurate 3D image may result in ablation in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Pemco Inc

Recalled Item: Rultract Retractor Ratchet Cover Plate Distributed by Pemco Recalled by...

The Issue: The firm became aware of the problem when a ratchet cover plate on a device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Smiths Medical ASD, Inc.

Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...

The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2013· Medical Indicators, Inc.

Recalled Item: Tempa DOT Single-Use Clinical Thermometer Medical Indicators Made in U.S.A....

The Issue: TempaDot products may have been mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2013· Medtronic Xomed, Inc.

Recalled Item: Tray Surgical Recalled by Medtronic Xomed, Inc. Due to The firm will recall...

The Issue: The firm will recall and replace the identified instrument trays in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2013· Philips Healthcare Inc.

Recalled Item: Radiohead Access Point 1.4 GHz Radiohead Access Point Firmware versions:...

The Issue: IntelliVue Smart-hopping 1.4 GHz Access Point may experience unexpected...

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

Class II — Potential Health HazardOngoing