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. 1,858 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,858 in last 12 months

Showing 2700127020 of 50,223 recalls

Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Scope ( Model 10967666) Recalled by Siemens Medical Solutions USA,...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Perspective (Model 10495568) Recalled by Siemens Medical Solutions...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing
FoodFebruary 1, 2018· J F C International Inc

Recalled Item: Daisho Kimchi Hot Pot Soup Base Recalled by J F C International Inc Due to...

The Issue: Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker Probe Cap Recalled by Cook Inc. Due to The interior of the...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker C02 Cartridge Recalled by Cook Inc. Due to The interior of the...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker Single Use Probe Recalled by Cook Inc. Due to The interior of...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker Sterilization Cap Recalled by Cook Inc. Due to The interior of...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker Pneumatic Lithotripter Recalled by Cook Inc. Due to The...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker Exhaust Line Recalled by Cook Inc. Due to The interior of the...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker Exhaust Cap Recalled by Cook Inc. Due to The interior of the...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2018· Howmedica Osteonics Corp.

Recalled Item: Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee...

The Issue: Customers may receive the incorrect size implant from what is labeled on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2018· Encore Medical, Lp

Recalled Item: AltiVate Reverse INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: Broken or missing screws and retaining clips. This may be due to screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Calcium Flex¿ reagent cartridge Recalled by Siemens...

The Issue: May produce erroneously low results from specific well sets.

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

Class II — Potential Health HazardOngoing
DrugJanuary 30, 2018· Millennium Pharmaceuticals Inc.

Recalled Item: VELCADE (bortezomib) for injection Recalled by Millennium Pharmaceuticals...

The Issue: Defective Container: Confirmed reports of loose vial crimps.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 30, 2018· Sumano's Bakery

Recalled Item: Sourdough Baguette: Product number 2064 Recalled by Sumano's Bakery Due to...

The Issue: Customer reported finding small metal piece similar to a BB on the outside...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 30, 2018· Sumano's Bakery

Recalled Item: Sourdough French: Product number 2044 Recalled by Sumano's Bakery Due to...

The Issue: Customer reported finding small metal piece similar to a BB on the outside...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 29, 2018· Stryker Communications

Recalled Item: Berchtold Chromophare Ceiling Mounted Surgical Light System Recalled by...

The Issue: The device could have a missing spanner nut and snap ring which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer System Recalled by Beckman Coulter Inc. Due to The...

The Issue: The device may process the same sample with two different sample IDs and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Encore Medical, Lp

Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...

The Issue: It was discovered during a surgery that the design of the radius at the base...

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

Class II — Potential Health HazardOngoing