Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,480 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,480 in last 12 months

Showing 1944119460 of 49,150 recalls

Medical DeviceJanuary 7, 2020· Stryker Corporation

Recalled Item: Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally Recalled...

The Issue: Sterile drapes packaged in an unsealed pouch.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Smiths Medical ASD, Inc.

Recalled Item: Portex ProVent Arterial Blood Sampling Kit with Dry Lithium Heparin Recalled...

The Issue: Lots of Smiths Medical Portex Pro-Vent and LineDraw Arterial Blood Sampling...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Smiths Medical ASD, Inc.

Recalled Item: Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin...

The Issue: Portex Pro-Vent and LineDraw Arterial Blood Sampling syringes may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· CME America, LLC

Recalled Item: CME America BodyGuard Infusion Pump System Recalled by CME America, LLC Due...

The Issue: Infusion Pump Systems may have a delivery inaccuracy of up to 13%, which may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 7, 2020· Zimmer Biomet, Inc.

Recalled Item: THP Hip Plating System Recalled by Zimmer Biomet, Inc. Due to Potential...

The Issue: Potential increase in fracture rate was detected during internal testing, in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Care Essentials Pty., Ltd.

Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...

The Issue: Potential for thermal damage near the power cord connector and Power Entry...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Care Essentials Pty., Ltd.

Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...

The Issue: Potential for thermal damage near the power cord connector and Power Entry...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Humidity Pack (Qty 5) Recalled by Siemens Healthcare...

The Issue: A software error is causing the analyzer to incorrectly eject affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Humidity Pack (Qty 1) Recalled by Siemens Healthcare...

The Issue: A software error is causing the analyzer to incorrectly eject affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· MEDTECH SAS

Recalled Item: ROSA Brain 3.0 Application-Brain Recalled by MEDTECH SAS Due to Some...

The Issue: Some cross-sectional images from the image acquisitions of the patients head...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· MEDTECH SAS

Recalled Item: ROSA One 3.1 Brain Application Recalled by MEDTECH SAS Due to Some...

The Issue: Some cross-sectional images from the image acquisitions of the patients head...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Zimmer Surgical Inc

Recalled Item: Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC...

The Issue: When inflating/deflating a single bladder, both bladders could potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Ethicon, Inc.

Recalled Item: Coated VICRYL (Polyglactin 910) Suture Recalled by Ethicon, Inc. Due to Some...

The Issue: Some sutures in the lot may exhibit a small section of braid fraying, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· Clinical Diagnostic Solutions, Inc.

Recalled Item: Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075...

The Issue: A mix-up of autosampler tube positions with a possibility of...

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

Class II — Potential Health HazardOngoing
FoodDecember 30, 2019· International Sprout Holding Inc.

Recalled Item: Clover seed in 50 lb. woven poly bags Recalled by International Sprout...

The Issue: Possible contamination with E. Coli.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 30, 2019· International Sprout Holding Inc.

Recalled Item: Clover seed in 55 lb. multi-layered white paper bags Recalled by...

The Issue: Possible contamination with E. Coli.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 30, 2019· Meijer

Recalled Item: Fresh From Meijer diced hard boiled eggs sold by weight Recalled by Meijer...

The Issue: Possible L. mono contamination in hard boiled eggs

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 30, 2019· Philips North America, LLC

Recalled Item: Integris Allura 9 Recalled by Philips North America, LLC Due to A capacitor...

The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 30, 2019· Philips North America, LLC

Recalled Item: Cardio Vascular-Allura Centron Recalled by Philips North America, LLC Due to...

The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 30, 2019· Philips North America, LLC

Recalled Item: UroDiagnost Eleva Recalled by Philips North America, LLC Due to A capacitor...

The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...

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

Class II — Potential Health HazardOngoing