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 2678126800 of 28,140 recalls

Medical DeviceNovember 12, 2012· Zimmer, Inc.

Recalled Item: Zimmer Spine Ardis Inserter Recalled by Zimmer, Inc. Due to Zimmer Spine has...

The Issue: Zimmer Spine has received reports of the PEEK Ardis Interbody Spacer...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 12, 2012· Greatbatch Medical

Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog...

The Issue: Greatbatch Medical observed some anomalies of the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare became...

The Issue: GE Healthcare became aware of a potential issue associated with the LOGIQ e...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2012· Cooper Vision Caribbean Corp.

Recalled Item: AVAIRA (enfilcon A) Soft (Hydrophilic) Daily Wear Toric Contact Lenses...

The Issue: The lenses exceeded the acceptance limit for silicone oil residual.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2012· Medtronic Neuromodulation

Recalled Item: SynchroMed EL Recalled by Medtronic Neuromodulation Due to Medtronic...

The Issue: Medtronic notified Healthcare Professionals of the impact of unapproved...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 9, 2012· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed II Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic notified Healthcare Professionals of the impact of unapproved...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 9, 2012· Philips Healthcare Inc.

Recalled Item: Philips IntelliVue Information Center/Client and Philips IntelliVue...

The Issue: Internal audio cable may have diminished retention force due to damaged...

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

Class II — Potential Health HazardOngoing