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. 1,027 recalls have been distributed to Hawaii in the last 12 months.
Showing 16501–16520 of 47,764 recalls
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...
The Issue: A new inspection step was added to the cleaning and disinfection section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Performance Verifier II-For in vitro diagnostic...
The Issue: Product instability; biased ALKP values obtained from VITROS Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elderberry Whole Organic Recalled by Starwest Botanicals, Inc Due to...
The Issue: Direct customer tested product upon receipt and had a positive result for...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Elderberry Whole Organic Recalled by Starwest Botanicals, Inc Due to...
The Issue: Direct customer tested product upon receipt and had a positive result for...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous...
The Issue: 5F Micro-Introducer Kits may not contain the correct device, packaged with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP Recalled by Luminex Corporation Due to Luminex has...
The Issue: Luminex has determined that three (3) separate test fixtures used by field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP Recalled by Luminex Corporation Due to Luminex has...
The Issue: Luminex has determined that three (3) separate test fixtures used by field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...
The Issue: There is a potential defect in the seals of the sterile barrier pouch used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard - Product Usage: Obstetric Gynecologic specialized manual instrument....
The Issue: Labeling error, incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas infinity central lab/cobas infinity core license-The cobas infinity IT...
The Issue: Potential Incorrect Validation of Results Due to an Erroneous QC Status When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminesse ML PMMA Recalled by Talladium Inc Due to Heat-cured...
The Issue: Heat-cured polymethylmethacrylate (PMMA) milling blank product used to make...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spice Hunter Black Pepper 1.7 oz. Jar Recalled by Sauer Brands Inc - SLO...
The Issue: Potential Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Spice Hunter Pumpkin Pie Spice 1.8 oz. Jar Recalled by Sauer Brands Inc...
The Issue: Potential Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Spice Hunter Cayenne Red Pepper 1.8 oz. Jar Recalled by Sauer Brands Inc...
The Issue: Potential Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.