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. 2,543 recalls have been distributed to Nebraska in the last 12 months.
Showing 15681–15700 of 28,140 recalls
Recalled Item: Medtronic EnTrust Escudo D144DRG (OUS distribution) Product Usage: The...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml...
The Issue: Label was incorrect. The label states that the volume of the retrieval bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Maestro 4000 Cardiac Ablation System Recalled by Boston...
The Issue: Reports of unintended continuation of radiofrequency (RF) energy delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Shepherd' s Hook - Greenberg Recalled by Nico Corp. Due to Mislabeling
The Issue: Mislabeled hook pouch included a transport/storage label rather than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...
The Issue: Through investigation, it was determined that H12LP Trocars in scope of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI system Product Usage: Hitachi MR system is Recalled by...
The Issue: The stainless steel belt which runs the length of the table underneath the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPAP Mask Cushion Recalled by Compass Health Brands (Corporate Office) Due...
The Issue: A May 2015 design change in the cushion seal replacement part and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J-Plasma Precise 360 Recalled by Bovie Medical Corporation Due to There is a...
The Issue: There is a potential risk associated with the PEEK tip of the J-Plasma...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Cleaning Brush Recalled by Medline Industries Inc Due to There is...
The Issue: There is potential risk of brush detachment during cleaning. If brush...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLISTA StandOP Surgical Light Recalled by Maquet SAS Due to Certain VOLISTA...
The Issue: Certain VOLISTA StandOP Surgical Lights have been identified as having a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoSPOT Recalled by Beekley Corporation Due to There is a potential for...
The Issue: There is a potential for imaging artifact to mimic calcifications on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun Temperature Management System Recalled by Bard Medical Division...
The Issue: An improper wiring connection on the chiller assembly may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-SPOT Recalled by Beekley Corporation Due to There is a potential for...
The Issue: There is a potential for imaging artifact to mimic calcifications on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Journey BCS Knee CoCr Femoral Components Recalled by Smith & Nephew, Inc....
The Issue: The data in the National Joint Registry of England, Wales and Northern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-SPOT Recalled by Beekley Corporation Due to There is a potential for...
The Issue: There is a potential for imaging artifact to mimic calcifications on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY BCS OXINIUM Knee Femoral Components Recalled by Smith & Nephew, Inc....
The Issue: The data in the National Joint Registry of England, Wales and Northern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY BCS Knee Conventional Polyethylene Inserts: 74023111 Recalled by...
The Issue: The data in the National Joint Registry of England, Wales and Northern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Biosystems HistoCore SPECTRA ST Recalled by Leica Microsystems, Inc....
The Issue: These devices have an incorrect specification against safety standard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2" Recalled by Teleflex...
The Issue: The incorrect plastic was used to manufacture the handles of these shears,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.