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. 1,065 recalls have been distributed to Nebraska in the last 12 months.
Showing 14421–14440 of 28,140 recalls
Recalled Item: IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a Recalled by Topcon...
The Issue: When a patient is selected in the patient data and another patient is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi NAV Suction Recalled by Acclarent, Inc. Due to The firm became aware...
The Issue: The firm became aware that three (3) lots of the NAV Suction Instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi NAV Suction Recalled by Acclarent, Inc. Due to The firm became aware...
The Issue: The firm became aware that three (3) lots of the NAV Suction Instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi NAV Suction Recalled by Acclarent, Inc. Due to The firm became aware...
The Issue: The firm became aware that three (3) lots of the NAV Suction Instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07...
The Issue: The firm has initiated a recall due to a confirmed complaint trend for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled...
The Issue: Based on internal investigations, Fresenius Kabi has identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07...
The Issue: The firm has initiated a recall due to a confirmed complaint trend for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile...
The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile...
The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 Coring Tool Recalled by Thoratec Corp. Due to Small...
The Issue: Small black plastic particle was observed in the left ventricle during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Sponge with the following product description and model numbers:...
The Issue: Potential lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnidiagnost Classic Recalled by Philips North America, LLC Due to The...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva w/ Flat Detector Recalled by Philips North America, LLC...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urodiagnost Recalled by Philips North America, LLC Due to The locking plate...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost-Eleva Recalled by Philips North America, LLC Due to The...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URODiagnost Eleva Recalled by Philips North America, LLC Due to The locking...
The Issue: The locking plate may be missing from the system, which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Small Diameter Cement Plug Inserter-Sterile Recalled by Zimmer...
The Issue: Lack of an adequate sterilization validation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.