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. 2,527 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,527 in last 12 months

Showing 2178121800 of 28,334 recalls

Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Wet Pak* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction Systems for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Multi-Access Port Replacement Catheter for Adults Recalled by...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Multi-Access Port Closed Suction System for Adults Recalled by...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Synthes (USA) Products LLC

Recalled Item: VEPTR Vertical Expandable Prosthetic Titanium Rib Recalled by Synthes (USA)...

The Issue: The last hole on certain VEPTR Inferior Cradles may be partially formed....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Neonates/Pediatrics Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Neonates/Pediatrics Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: KimVent* Wet Pak* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Halyard Health, Inc

Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...

The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes Trauma Ex-Fix System (Small Recalled by Synthes (USA) Products LLC...

The Issue: Labeling changes were made related to MR conditions that align with standard...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2015· Beckman Coulter Inc.

Recalled Item: Access Thyroglobulin Assay Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter, Inc. is recalling Access Thyroglobulin reagent packs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 28, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Blood Gas Analyzer Recalled by Siemens Healthcare Diagnostics...

The Issue: When both ports (Serial and Ethernet) are configured to transmit data, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...

The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Sunrise Medical (US) LLC

Recalled Item: Zippie IRIS Wheelchair. model EIZ5A in combination with option code Recalled...

The Issue: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest...

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

Class II — Potential Health HazardOngoing