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. 2,491 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,491 in last 12 months

Showing 1878118800 of 49,150 recalls

Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: CRANIOSCULPT C Recalled by Skeletal Kinetics, Llc Due to Bone void filler...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: CRANIOSCULPT C Recalled by Skeletal Kinetics, Llc Due to Bone void filler...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: CRANIOSCULPT FLOW Recalled by Skeletal Kinetics, Llc Due to Bone void filler...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: MEDTRONIC BONE VOID FILLER Recalled by Skeletal Kinetics, Llc Due to Bone...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: CRANIOSCULPT Recalled by Skeletal Kinetics, Llc Due to Bone void filler kits...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: CRANIOSCULPT Recalled by Skeletal Kinetics, Llc Due to Bone void filler kits...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: OSTEOVATIONEX Recalled by Skeletal Kinetics, Llc Due to Bone void filler...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: CRANIOSCULPT FLOW Recalled by Skeletal Kinetics, Llc Due to Bone void filler...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: OSTEOVATION Recalled by Skeletal Kinetics, Llc Due to Bone void filler kits...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: SKAFFOLD RENU FLOW Recalled by Skeletal Kinetics, Llc Due to Bone void...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: SK SKAFFOLD IMPRESS 10CC. Product Number: SKAF-IM10 Recalled by Skeletal...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: OSTEOVATION Recalled by Skeletal Kinetics, Llc Due to Bone void filler kits...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: ACUMED IMPACT 10CC. Product Number: 65-0110-S Recalled by Skeletal Kinetics,...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: ACUMED IMPACT 5CC. Product Number: 65-0105-S Recalled by Skeletal Kinetics,...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: OSTEOVATION EX Recalled by Skeletal Kinetics, Llc Due to Bone void filler...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: EXACTECH OSSILIX FORM (MX) Recalled by Skeletal Kinetics, Llc Due to Bone...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: EXACTECH OSSILIX FORM (MX) Recalled by Skeletal Kinetics, Llc Due to Bone...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Skeletal Kinetics, Llc

Recalled Item: SKAFFOLD RENU FLOW Recalled by Skeletal Kinetics, Llc Due to Bone void...

The Issue: Bone void filler kits may not maintain its setting characteristics for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2020· Agfa N.V.

Recalled Item: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Recalled...

The Issue: Under specific conditions (Fluoroscopic exam, ABS=OFF, manual change of...

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

Class II — Potential Health HazardOngoing
DrugApril 3, 2020· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Golden State Medical Supply Inc. Due...

The Issue: CGMP Deviations: Impurity for N-nitroso-N-methyl-4-aminobutryric Acid (NBMA)...

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

Class II — Potential Health HazardOngoing
Refund