Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,486 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,486 in last 12 months

Showing 1612116140 of 27,462 recalls

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
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· 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· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack: 1) UDI-M535SAK3010 Recalled by NxStage Medical, Inc....

The Issue: May contain endotoxin levels which have been confirmed to exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2018· Philips Electronics North America Corporation

Recalled Item: Philips QCPR Meter - used with FR3 Product Usage: The Recalled by Philips...

The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...

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

Class II — Potential Health HazardOngoing
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· Philips Electronics North America Corporation

Recalled Item: Philips QCPR Meter - used with MRx Product Usage: The Recalled by Philips...

The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...

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
Medical DeviceJanuary 26, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: Ray Station 4.9 Ray Station 5 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: Software issue with Center Beam in Field functionality. Issue can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2018· bioMerieux, Inc.

Recalled Item: bioMerieux VITEK 2 Gram Positive Cefoxitin Screen Recalled by bioMerieux,...

The Issue: Customer reports indicated an increase in the rate of non-detected MRSA in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 26, 2018· Stryker Communications

Recalled Item: Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel Recalled...

The Issue: The mounts on the monitor may have an insufficient (missing or incomplete) weld.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: Biograph Horizon - PET/CT Recalled by Siemens Medical Solutions USA, Inc....

The Issue: Error introduced into PET images acquired and reconstructed with VJ20A...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2018· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound System Product Usage: The SC2000 ultrasound imaging...

The Issue: The application may underestimate the EROA (Effective Regurgitant Orifice...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: O-arm 1000 mobile image-intensified fluoroscopic x-ray system Recalled by...

The Issue: Software update ("SW Update 3.2.1") is being implemented to address the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2018· GE Healthcare

Recalled Item: Centricity Universal Viewer Product Usage: Usage: Centricity PACS-IW with...

The Issue: Potential that one or more image series may be missing from an exam without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2018· GE Healthcare

Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity...

The Issue: Potential that one or more image series may be missing from an exam without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Liberty Select Cycler (SW v.2.8.7) Recalled by Fresenius Medical Care Renal...

The Issue: The recalling firm identified a software issue related to the Patient Line...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2018· 3M Company - Health Care Business

Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...

The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...

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

Class II — Potential Health HazardOngoing