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. 1,682 recalls have been distributed to Hawaii in the last 12 months.
Showing 40641–40660 of 47,764 recalls
Recalled Item: ADVIA Centaur Systems TSH3 Ultra Ready Pack Recalled by Siemens Healthcare...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems VitD 500 test Recalled by Siemens Healthcare...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Potential for biased...
The Issue: Potential for biased results when a Multiple Window (MW) code is associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems BRAHMS PCT 100 test Sold only OUS Recalled by Siemens...
The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae Recalled by...
The Issue: Potential for separation of dilator tips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae with Duraflo...
The Issue: Potential for separation of dilator tips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When the E-NMT-01 module...
The Issue: When the E-NMT-01 module is used in conjunction with the ElectroSensor, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cochlear Baha Soft tissue gauge 6mm. Reusable instrument used to Recalled by...
The Issue: Cochlear America is recalling Cochlear Baha Soft Tissue Gauge due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bissinger's Dark Chocolate Bunny Ears Recalled by Karl Bissinger LLC Due to...
The Issue: Milk chocolate bunny ears are packaged in dark chocolate packaging. The...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: THINOGENICS Recalled by Nature's Universe Due to Undeclared Sibutramine
The Issue: Marketed Without an Approved NDA/ANDA: Product contains undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Children's Cetirizine Hydrochloride Chewable Tablets Recalled by Caraco...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine Hydrochloride Chewable Tablets Recalled by Caraco Pharmaceutical...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tikosyn¿ (dofetilide) 500 mcg (0.5mg) capsules Recalled by Pfizer Inc. Due...
The Issue: Presence of Foriegn Tablets/Capsules: A single Tikosyn¿ (dofetilide) 250 mcg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: e.cam -emission computed tomography system Used to detect or image Recalled...
The Issue: There is a potential for patient finger injury on the e.cam systems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Combo Panel Type 33 (PC33): Catalog number B1017-211 Recalled...
The Issue: Siemens investigation confirmed that a portion one lot of panel Pos Combo 33...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intended for both adult and pediatric patients for taking diagnostic...
The Issue: In special cases, during the start-up of the current model of MobileDiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)...
The Issue: Separation events have occurred, including the VIPR separating from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SBi RingFix Olive Wires Product Usage: These are temporary devices Recalled...
The Issue: Small Bone Innovations (SBI) is recalling non-sterile RingFIX Olive Wires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipase Reagent Recalled by Abbott Laboratories, Inc Due to Package inserts...
The Issue: Package inserts have incorrect SmartWash parameters for Triglyceride.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.