Product Recalls in Hawaii
Product recalls affecting Hawaii — including food, drugs, consumer products, medical devices, and vehicles distributed to Hawaii. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,391 recalls have been distributed to Hawaii in the last 12 months.
Showing 23041–23060 of 27,645 recalls
Recalled Item: STAT 2 Flow Controller Recalled by ICU Medical, Inc. Due to ICU is recalling...
The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 98" (249 cm) Appx 12.3 ml Recalled by ICU Medical, Inc. Due to ICU is...
The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 83" (211 cm) Appx 10.3 mL Recalled by ICU Medical, Inc. Due to ICU is...
The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens CentraLink Data Management System Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has identified a task scheduler issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse Implantable Cardioverter Defibrillators (ICDs) Recalled by St Jude...
The Issue: An anomaly may result in delayed, partial, or no delivery of high voltage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT 2 Flow Controller Recalled by ICU Medical, Inc. Due to ICU is recalling...
The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Support Material Number: 9890 010 87431 Recalled by Philips Medical...
The Issue: The hook does not securely hold the footplate in vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Support Material Number: 9890 010 87431 used with: BuckyDiagnost...
The Issue: The hook does not securely hold the footplate in vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista¿ CHEM 1 CAL Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has received complaints for low recovery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon Oval MRI system is a diagnostic imaging device Recalled by...
The Issue: The Gradient Coil was found to have a failure mode that allowed it to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FOCAL Sim Workstation Recalled by Elekta, Inc. Due to When DICOM is...
The Issue: When DICOM is exporting an arc plan (VMAT, Dynamic Conformal of 3D Static...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco The Monaco system is used to make treatment plans Recalled by Elekta,...
The Issue: Incorrect Delivery of Composite VMAT Fields - When DICOM is exporting an arc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4D Integrated Treatment Console (4DITC) Recalled by Varian Medical Systems,...
The Issue: Due to user error, the 4DITC can improperly allow users to clear a safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below...
The Issue: Potential issues with the ProVue driver have been identified which may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Array LaserLink Recalled by Lumenis, Inc. Due to Lumenis initiated a...
The Issue: Lumenis initiated a field-correction for the Array Laser Link",...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics RESTORATION Acetabular Augment System Recalled...
The Issue: The peel strength of the inner blister may have been below internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp....
The Issue: The peel strength of the inner blister may have been below internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp....
The Issue: The peel strength of the inner blister may have been below internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Electric Drive (SED). For use in general traumatology....
The Issue: The affected Small Electric Drive (SED) may operate solely in reverse mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAM Junctional Tourniquet (SJT) Auxiliary Recalled by Sam Medical Products...
The Issue: SAM Junctional Tourniquet (SJT) Auxiliary strap, model SJT 102 and SJT 112,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.