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. 1,077 recalls have been distributed to Hawaii in the last 12 months.
Showing 9141–9160 of 27,645 recalls
Recalled Item: ECHELON Oval MRI System Recalled by Hitachi Healthcare Americas Corporation...
The Issue: There was no label on the pad packaging or notification in the user manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit ( by Sentinel CH...
The Issue: Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANA/PROFx CLASSIC FEMORAL HOOK RIGHT Recalled by Mizuho OSI Due to One...
The Issue: One batch of "regular" femoral hooks were incorrectly etched with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Trinity Dual Mobility Recalled by Corin Ltd Due to The packaging...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin MetaFix Hip Stem Recalled by Corin Ltd Due to The packaging system on...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin TriFit TS Recalled by Corin Ltd Due to The packaging system on the...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek SmartView Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Test strip vials may open while inside sealed cartons during shipment. An...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Aviva Plus Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Test strip vials may open while inside sealed cartons during shipment. An...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Inform II Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Test strip vials may open while inside sealed cartons during shipment. An...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Processor 3K Recalled by Beckman Coulter Inc. Due to Missing splash...
The Issue: Missing splash guard which may expose users to hazardous materials. .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Trinity Screw Recalled by Corin Ltd Due to The packaging system on the...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Trinity-i Recalled by Corin Ltd Due to The packaging system on the...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Test strip vials may open while inside sealed cartons during shipment. An...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee CS Insert Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Trinity Liner ECIMA Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX Delta Mod Head Recalled by Corin Ltd Due to The packaging...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee Augments Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Unity Knee Patella Recalled by Corin Ltd Due to The packaging system...
The Issue: The packaging system on the devices have potential physical and water damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Status COVID-19/Flu Rapid Immunoassay for Direct Detection and Differential...
The Issue: Products may have been distributed to customers other than laboratories...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Peripheral Vascular Inc Due to Potential for needle...
The Issue: Potential for needle protector to become fully dislodge exposing infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.