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. 2,412 recalls have been distributed to Hawaii in the last 12 months.
Showing 21261–21280 of 27,645 recalls
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert CT/NG Urine Specimen Collection Kit Part number GXCT/NGURINE-50...
The Issue: Firm determined that some lots of CT/NG Swab 50 and CT/NG Urine collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIDEX Activated Dialdehyde Solution Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization Products (ASP) is recalling the CIDEX Activated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit: Part number...
The Issue: Firm determined that some lots of CT/NG Swab 50 and CT/NG Urine collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due...
The Issue: EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista B¿2-Microglobulin Flex Reagent Cartridge (B2MIC) Recalled by...
The Issue: customers are receiving a high number of Abnormal Assay Errors or are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips GoSafe Mobile Help Button Recalled by Lifeline Systems, Incorporated...
The Issue: Irregular battery disconnection resulted in issues with Mobile Health Button...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Pioneer Plus Re-Entry Catheter Recalled by Volcano Corporation Due...
The Issue: Due to a manufacturing defect, there is the possibility that a small wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Application Instrument for Sternal ZIPFIX Recalled by Synthes (USA)...
The Issue: The end cap may loosen and detach making the instrument non-functional. No...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER LH Series Diluent Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Lineum OCC Starter Flexible and Lineum Flexible Inner Shaft...
The Issue: Biomet has initiated a recall on Biomet Spine Lineum OCC Starter Flexible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER ISOTON 4 Diluent Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the LH 750 and LH780 Hematology Systems because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Kinetics Recalled by Neuro Kinetics, Inc. Due to The devices that...
The Issue: The devices that included the OVAR research test were not cleared for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to Channel Error...
The Issue: Channel Error code is displayed on the PC unit with an audio and visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CrossCHECK Non-Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CrossCHECK Locking Screw in the following sizes: 3.0 x 8 mm Recalled by...
The Issue: These screws have a potential of passing through the plate in the case when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune 2 Waste Management System Docking Station (120V and 230V) Recalled...
The Issue: The Fluid Coupling Sleeve, a component within the Neptune Waste Management...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concave Reamer Head Recalled by Trilliant Surgical Ltd. Due to The...
The Issue: The cannulation of the Concave and Convex Reamer Heads may be too small to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tiger Cannulated Tray Lid Part # 210-00-001-1 NON-STERILE Recalled by...
The Issue: Sterilization tray lids for the Tiger and Tiger Headless Cannulated Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and...
The Issue: The cutting efficiency of the Countersinks was out of specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.