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.
Showing 23221–23240 of 28,140 recalls
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONMED PEDIATRIC R2 Multifunction Electrodes Recalled by ConMed Corporation...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI PEDIATRIC Radiotransparent Electrode Recalled by ConMed Corporation Due...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Healon EndoCoat Ophthalmic Viscosurgical Device 3% sodium hyaluronate...
The Issue: AMO has received complaints where the finger grip dislodged while depressing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CHEMISTRY PRODUCTS TRIG Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Potential for biased results using the specific lot of VITROS CHEMISTRY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEDIATRIC Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Electric Drive (SED) Recalled by Synthes (USA) Products LLC...
The Issue: The device may operate solely in reverse mode, not operate in reverse mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A...
The Issue: Potential problem with the cardiac function analysis software (CFA)....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polyflux Revaclear Dialyzer Recalled by Gambro Renal Products Inc Due to...
The Issue: Gambro is initiating a field action for Polyflux Revaclear Dialyzer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polyflux Revaclear Max Dialyzer Recalled by Gambro Renal Products Inc Due to...
The Issue: Gambro is initiating a field action for Polyflux Revaclear Dialyzer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A...
The Issue: Potential problem with the cardiac function analysis software (CFA)....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile drape Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUNA Chest Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulsiocath PiCCO ProAQT Monitoring Kit Recalled by Pulsion Medical Inc Due...
The Issue: Internal testing and investigation of the packaging revealed cracks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Silhouette and/or MiniMed Sure-T Infusion Sets Recalled by...
The Issue: Tubing may detach at the connect/disconnect location on the MiniMed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.