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 1846118480 of 28,140 recalls

Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Hips Active Articulation ArComXL Bearings...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2017· Crossroads Extremity Systems Llc

Recalled Item: MotoCLIP(TM) Super Elastic Fusion System Recalled by Crossroads Extremity...

The Issue: Seven 18mm x 18mm x 18 mm implants had been placed in kits, packed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2017· Merit Medical Systems, Inc.

Recalled Item: 7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070 Recalled by...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for sheaths...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 15, 2017· IntroMedic Co., Ltd.

Recalled Item: Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule...

The Issue: When a user switches on MR1100 Receiver, even though the battery was fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2017· Baxter Healthcare Corporation

Recalled Item: Prismaflex Control Unit. Dialyzer Recalled by Baxter Healthcare Corporation...

The Issue: Firm has received reports of device operators failing to adhere to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2017· Euro Diagnostica AB

Recalled Item: Euro Diagnostica DIASTAT ANA (anti-nuclear antibody) ELISA DIASTAT ANA...

The Issue: Euro Diagnostica has identified a deviation in one of the components of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2017· Zimmer Biomet, Inc.

Recalled Item: Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital...

The Issue: Digital templates were created with the incorrect files.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2017· Olympus Corporation of the Americas

Recalled Item: Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II...

The Issue: A damaged temperature sensor at the endoscope's tip can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Smiths Medical ASD Inc.

Recalled Item: Bivona¿ TTS (Tight to Shaft) Pediatric Tracheostomy Tube Recalled by Smiths...

The Issue: Smiths Medical became aware that one lot of the Bivona¿ 3.5mm TTS Cuffed...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...

The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Remel Inc

Recalled Item: Remel Recalled by Remel Inc Due to Test organisms exhibit poor growth when...

The Issue: Test organisms exhibit poor growth when grown using the test agar. The poor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Del Mar Reynolds Medical, Ltd.

Recalled Item: Arkon Anesthesia Delivery System Recalled by Del Mar Reynolds Medical, Ltd....

The Issue: Spacelabs has received reports of the Arkon Anesthesia Delivery System,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter (eIFU) REF# e2400-50...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter with...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF #...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter (eIFU) REF#...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter with Introducer...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing