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. 2,450 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,450 in last 12 months

Showing 2458124600 of 49,150 recalls

Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: Capnostream20 N W/PRINTER CYVITAL Recalled by Oridion Medical 1987 Ltd. Due...

The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: Capnostream20 (INTL) N W/PRINTER Recalled by Oridion Medical 1987 Ltd. Due...

The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: Capnostream20 M ADULT ICU (CPM) Recalled by Oridion Medical 1987 Ltd. Due to...

The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: CAPNOSTREAM 20P (US) N - ROHS Recalled by Oridion Medical 1987 Ltd. Due to...

The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2018· Oridion Medical 1987 Ltd.

Recalled Item: Capnostream20 N CYVITAL Recalled by Oridion Medical 1987 Ltd. Due to The...

The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2018· Zimmer Biomet Spine Inc.

Recalled Item: Vitality¿ Spinal Fixation System. Spinal Interlaminal Recalled by Zimmer...

The Issue: The Vitality Shear-off Set Screw is not threading properly with the mating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2018· Zimmer Biomet Spine Inc.

Recalled Item: Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system...

The Issue: The Vitality Shear-off Set Screw is not threading properly with the mating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2018· Zimmer Biomet Spine Inc.

Recalled Item: Vitality¿ Spinal Fixation System.Spinal Intervertebral Body Recalled by...

The Issue: The Vitality Shear-off Set Screw is not threading properly with the mating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2018· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Complaints received of sporadic erroneously elevated platelet results...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2018· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Complaints received of sporadic erroneously elevated platelet results...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2018· Beckman Coulter Inc.

Recalled Item: UniCel DxH 900 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Complaints received of sporadic erroneously elevated platelet results...

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

Class I — Serious Health HazardOngoing
DrugJuly 30, 2018· MAJOR PHARMACEUTICALS

Recalled Item: Doxycycline Hyclate Tablets Recalled by MAJOR PHARMACEUTICALS Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Pheno Interventional Fluoroscopic X-Ray System Recalled by Siemens...

The Issue: Temperature of the detector may fall out of its designed working range (cool...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q Interventional Fluoroscopic X-Ray System Recalled by Siemens Medical...

The Issue: Temperature of the detector may fall out of its designed working range (cool...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2018· Sysmex America, Inc.

Recalled Item: Sysmex XN-Series Fluorocell PLT Recalled by Sysmex America, Inc. Due to The...

The Issue: The fluorescent platelet counts (PLT-F) and immature platelet fraction (IPF)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2018· Stryker Sustainability Solutions

Recalled Item: Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers...

The Issue: Affected lots of reprocessed arthroscopic shavers may display the incorrect...

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

Class II — Potential Health HazardOngoing
FoodJuly 27, 2018· Fresh Express Incorpated

Recalled Item: McDonalds Salad Ingredients Recalled by Fresh Express Incorpated Due to...

The Issue: Fresh Express initiates a recall of expired foodservice salad products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 27, 2018· Fresh Express Incorpated

Recalled Item: McDonald s Whole Green Leaf Salad 1 lb Recalled by Fresh Express Incorpated...

The Issue: Fresh Express initiates a recall of expired foodservice salad products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 27, 2018· Fresh Express Incorpated

Recalled Item: Fresh Express Chopped Romaine 1 lb Recalled by Fresh Express Incorpated Due...

The Issue: Fresh Express initiates a recall of expired foodservice salad products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 26, 2018· Confidence Inc./Confidence U.S.A. Inc.

Recalled Item: FP0392 Recalled by Confidence Inc./Confidence U.S.A. Inc. Due to Undeclared...

The Issue: Product contains undeclared ingredients, Hydroxypropyl Methylcellulose...

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

Class III — Low RiskOngoing
Refund