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 22121–22140 of 47,764 recalls
Recalled Item: Nova Salted Biscuit The product comes in a 14.08 ounce Recalled by Asia Food...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Integrated ECG cable with 3-lead leadwires labeled as the following:...
The Issue: The Integrated ECG cable with 3-lead leadwires can short circuit during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxybutynin Chloride Recalled by Lannett Company Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Smith&Nephew SmartStitch PerfectPasser Connector Recalled by ArthroCare...
The Issue: The voluntary recall is being initiated due to a manufacturing error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical ChemoLock Closed Vial Spike w/Skirt Recalled by ICU Medical, Inc....
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SetSource ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical Oncology Kit w/12" (30cm) Ext Set w/Spiros w/Red Cap Recalled by...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical ChemoLock Recalled by ICU Medical, Inc. Due to There is a...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical Oncology Kit w/12" Ext Set w/Spiros w/Red Cap Recalled by ICU...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage: BD...
The Issue: BD Synapsys version 2.1 allowed the potential for a test order to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clear plastic Recalled...
The Issue: Undeclared soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VITROS¿ 3600 Immunoassay System-Software V3.3.2 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ ECi/ECiQ Immunodiagnostic System Product Code: 1922814 For use in...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 5600 Integrated System -Software V3.3.2 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 5600 Integrated System V3.3.2 & below Product Code: Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS ECi Immunodiagnostic System Product Code: 6801059 For use Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ XT 7600 Integrated System-Software V3.4.1 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 3600 Immunoassay System V3.3.2 & below Product Code: Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.