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. 2,480 recalls have been distributed to Hawaii in the last 12 months.
Showing 15361–15380 of 27,645 recalls
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...
The Issue: The analyzer software may cause a mis-match of patient demographics and test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device Recalled...
The Issue: Bubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended Recalled...
The Issue: Incorrect expiration being entered for one lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Waterpik Sonic-Fusion Professional Recalled by Water Pik, Inc. Due to...
The Issue: Charging base may overheat with localized melting and sparking, possibly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTOVi Tracker/Scanner Recalled by Hudson Scientific LLC Due to The device...
The Issue: The device and its accessories may not have been manufactured according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Powder Free Vinyl Exam Gloves Recalled by Cypress Medical Products LLC Due...
The Issue: The firm is recalling one lot of McKesson Powder Free Vinyl Exam Gloves...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 Recalled by...
The Issue: An incorrect control board and firmware installed in some of the Hand Held...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer (SMN 11066000). The Atellica" Solution is Recalled...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Additional (SMN 11069004). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Connect (SMN 11069018). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer (SMN 11066001). The Atellica" Solution is Recalled...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer (SMN 11067000) . The Atellica" Solution Recalled by...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pure Rayz Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not receive...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quasar MD Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.