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. 2,457 recalls have been distributed to Hawaii in the last 12 months.
Showing 17821–17840 of 47,764 recalls
Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Premium Urine Meter Foley Tray Recalled by Covidien Llc...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 400mL Recalled by Covidien Llc Due to Temperature sensing catheters...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Incubator with installed Servo Oxygen module. Infant incubator....
The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and...
The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benefiber Healthy Shape Prebiotic Fiber Supplement Recalled by...
The Issue: Fiber prebiotic product potentially contaminated with small plastic pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Prebiotic Fiber Supplement Recalled by Glaxosmithkline Consumer...
The Issue: Fiber prebiotic product potentially contaminated with small plastic pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DDU-2300 Lifeline/ReviveR View Recalled by Defibtech, LLC Due to A component...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A Recalled...
The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-2400EN Lifeline PRO Recalled by Defibtech, LLC Due to A component issue...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Disposable Connectors ASY STR CONN 1/4 STRLE 24. REF/ Recalled by...
The Issue: The firm has identified through internal tests that the sterile barrier of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Disposable Connectors ASY S CONN 3/16X1/8 RDR ANLD24 REF/ Recalled...
The Issue: The firm has identified through internal tests that the sterile barrier of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT iGentamicin Reagent Kit - Product Usage: The measurements obtained...
The Issue: Abbott identified that samples tested for ARCHITECT STAT High Sensitive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant/Child Reduced Energy Defibrillation Electrodes Recalled by...
The Issue: Packaging of infant child reduced energy electrodes was not properly sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Child Starter Kits Recalled by Physio-Control, Inc. Due to Packaging...
The Issue: Packaging of infant child reduced energy electrodes was not properly sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Bone Void Filler Recalled by Medtronic Sofamor Danek USA Inc Due...
The Issue: Product may not maintain its setting characteristics for the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extremities Recalled by Medtronic Sofamor Danek USA Inc Due to Product may...
The Issue: Product may not maintain its setting characteristics for the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Bone Void Filler Recalled by Medtronic Sofamor Danek USA Inc Due...
The Issue: Product may not maintain its setting characteristics for the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.