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. 999 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
999 in last 12 months

Showing 29181–29200 of 50,223 recalls

Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Radiology CT (Model No. 728244) software version...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Cenorin, LLC

Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....

The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core (Model No. 728321) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT (Model No. 728332) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Spectranetics Corporation

Recalled Item: Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid...

The Issue: Potential for flouroscopially visible marker band at the tip of the Rapid...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q and Q.Zen Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for liquid entry

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee and Zeego Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for liquid entry

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

Class II — Potential Health HazardOngoing