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. 2,040 recalls have been distributed to Hawaii in the last 12 months.
Showing 3041–3060 of 47,764 recalls
Recalled Item: THORACIC PACK Recalled by American Contract Systems Inc Due to ACS is unable...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis: Anesthesia Station ES Recalled by CareFusion 303, Inc. Due to Sync...
The Issue: Sync timeout may occur between the server and automated dispensing device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol Gel Recalled by Padagis US LLC Due to Defective Container: Some...
The Issue: Defective Container: Some packets may not be fully sealed, potentially...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAJOR DIEP Recalled by American Contract Systems Inc Due to ACS is unable to...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters...
The Issue: Devices may have higher than expected amounts of bacterial endotoxin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URO ROBOTIC PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CV BASIC PUMP PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURORA Surgiscope System Recalled by Integra LifeSciences Corp. Due to...
The Issue: Possibility for the obturator to break (separate).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BORN ON ARRIVAL KIT Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENERAL ANGIO PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA Recalled by...
The Issue: Unexpected loose material in the male luer used in the aortic root cannula...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion System (V6 Platform) Recalled by Baxter...
The Issue: There is the potential for missing motor mounting screws, which may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...
The Issue: There is the potential for missing motor mounting screws, which may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Feel Good Foods Recalled by FEEL GOOD FOODS INC Due to Foreign Object...
The Issue: Foreign object (metal pieces).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Access 2 Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter identified that an issue for Access 2 Sample Motors (B48016)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotarex Atherectomy System and Instructions for Use Recalled by Bard...
The Issue: Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelePACS (Image Fusion Module) - InteleViewer Recalled by INTELERAD...
The Issue: A software application that receives digital images and data from various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDITECH Expanse Laboratory (LAB) Recalled by Medical Information...
The Issue: Entering multiple keys that trigger input simultaneously may remove data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.