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. 2,375 recalls have been distributed to Hawaii in the last 12 months.
Showing 27161–27180 of 27,645 recalls
Recalled Item: Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R)...
The Issue: Lidstock of product does not contain chlorhexidine contraindication and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical NUVO LITE MODEL 925 OCSI Recalled by Nidek Medical Products...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical NUVO LITE MODEL 520 STD Recalled by Nidek Medical Products Inc...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical M5C5/ MARK5 NUVO/STD Recalled by Nidek Medical Products Inc...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical MARK5 NUVO 8 STD Recalled by Nidek Medical Products Inc Due to...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical MARK5 NUVO 8 /OCSI Recalled by Nidek Medical Products Inc Due...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical NUVO LITE MODEL 925 OCSI Recalled by Nidek Medical Products...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical M5C5/ MARK5 NUVO/OCSI Recalled by Nidek Medical Products Inc...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical NUVO LITE MODEL 525 OCSI Recalled by Nidek Medical Products...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical MARK5 NUVO / M5C5 Recalled by Nidek Medical Products Inc Due...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray...
The Issue: During regular product monitoring, firm became aware of a potential issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextgen Complete Knee Solution Femoral and Provisional Impactor/ Extractor...
The Issue: The design of the spring clip for the jaw assembly was updated in March 2011...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Uroskop Access. Fluoroscopic Recalled by Siemens Medical Solutions...
The Issue: Siemens has discovered a possible hazard to patients or hospital personnel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABG II Modular Hip Stem Stryker Howmedica Osteonics Corp. Mahwah Recalled by...
The Issue: Stryker has updated the instruction for use (IFU) (product correction)for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rejuvenate Modular Stems Stryker Ireland Carrigtwohill Industrial Estate...
The Issue: Stryker has updated the instruction for use (IFU) (product correction)for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextgen Complete Knee Solution Replacement Jaw for Use with Femoral Recalled...
The Issue: The design of the spring clip for the jaw assembly was updated in March 2011...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CM Flowmeter Pkg H Recalled by Accutron Inc Due to Accutron is recalling the...
The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport Portable Package Recalled by Accutron Inc Due to Accutron is...
The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra PC% Cabinet Mount Package G Recalled by Accutron Inc Due to Accutron...
The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Meter Recalled by Accutron Inc Due to Accutron is recalling the...
The Issue: Accutron is recalling the Flowmeter (Analgesia Gas Machine) because when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.