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. 2,439 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,439 in last 12 months

Showing 2580125820 of 49,150 recalls

Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Motorized) Recalled by FHC, Inc. Due to...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Anika Therapeutics, Inc.

Recalled Item: Hyalomatrix Recalled by Anika Therapeutics, Inc. Due to Hyalomatrix products...

The Issue: Hyalomatrix products are susceptible to degradation as a result of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2018· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: ImagePilot Recalled by Konica Minolta Medical Imaging USA, Inc. Due to...

The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHYT Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: There is a potential for imprecise results when using the slides. Increase...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2018· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: CS-7 Recalled by Konica Minolta Medical Imaging USA, Inc. Due to Panasonic...

The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Human Design Medical Llc

Recalled Item: Vivo 65 Recalled by Human Design Medical Llc Due to Some Vivo 65 devices...

The Issue: Some Vivo 65 devices have an unreleased version of the Firmware upgrade tool.

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

Class III — Low RiskOngoing
Medical DeviceMay 8, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...

The Issue: The firm will be updating the Instructions for Use for the product. Current...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Wescam Inc

Recalled Item: MX-10 surveillance laser system Product Usage: The expected usage of...

The Issue: Product has a nominal ocular hazard distance (NOHD) that is longer than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Zeiss, Carl Inc

Recalled Item: Cell Observer SD Recalled by Zeiss, Carl Inc Due to In certain eyepiece...

The Issue: In certain eyepiece configurations the laser shutter may not close...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Stryker Sustainability Solutions

Recalled Item: Reprocessed HARMONIC Ace¿ +7 Recalled by Stryker Sustainability Solutions...

The Issue: Stryker Sustainability Solutions has received an increase in reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...

The Issue: The firm will be updating the Instructions for Use for the product. Current...

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

Class II — Potential Health HazardOngoing
DrugMay 8, 2018· Apotex Inc.

Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Apotex Inc. Due to...

The Issue: Subpotent Drug: High Levels of Impurities Resulting in Decrease Potency

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 8, 2018· Apotex Inc.

Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Apotex Inc. Due to...

The Issue: Subpotent Drug: High Levels of Impurities Resulting in Decrease Potency

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 7, 2018· RIJ Pharmaceutical LLC

Recalled Item: SDA Senna Syrup (Sennosides 8.8mg) Recalled by RIJ Pharmaceutical LLC Due to...

The Issue: CGMP Deviations: Products are being recalled due to an out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 7, 2018· RIJ Pharmaceutical LLC

Recalled Item: Geritrex Senna Syrup (sennosides 8.8mg) Recalled by RIJ Pharmaceutical LLC...

The Issue: CGMP Deviations: Products are being recalled due to an out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 7, 2018· RIJ Pharmaceutical LLC

Recalled Item: Preferred Plus Pharmacy Antacid Extra Strength (Aluminum Hydroxide 400mg...

The Issue: CGMP Deviations: Products are being recalled due to an out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 7, 2018· RIJ Pharmaceutical LLC

Recalled Item: RPC Children's Non-Aspirin (Acetaminophen 160 mg) Elixir Recalled by RIJ...

The Issue: CGMP Deviations: Products are being recalled due to an out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 7, 2018· RIJ Pharmaceutical LLC

Recalled Item: Gericare Liquid Pain Relief Acetaminophen Cherry Flavor 160mg/5mL Recalled...

The Issue: CGMP Deviations: Products are being recalled due to an out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 7, 2018· RIJ Pharmaceutical LLC

Recalled Item: RPC Senna Syrup (Sennosides 8.8mg) Recalled by RIJ Pharmaceutical LLC Due to...

The Issue: CGMP Deviations: Products are being recalled due to an out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 7, 2018· RIJ Pharmaceutical LLC

Recalled Item: Gericare Iron Supplement Elixir Ferrous Sulfate 220 mg Recalled by RIJ...

The Issue: CGMP Deviations: Products are being recalled due to an out of specification...

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

Class II — Potential Health HazardOngoing
Refund