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. 2,338 recalls have been distributed to Hawaii in the last 12 months.
Showing 35621–35640 of 47,764 recalls
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: 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 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: Phentermine Hydrochloride Capsules Recalled by PD-Rx Pharmaceuticals, Inc....
The Issue: Failed impurities/Degradation specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Verapamil Hydrochloride Extended-Release tablets Recalled by Apotex Inc. Due...
The Issue: Failed Dissolution Specification: One lot of product did not meet the first...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ALLOPURINOL TABLETS Recalled by Qualitest Pharmaceuticals Due to Failed...
The Issue: Failed Tablet/Capsule Specifications; report of oversized and discolored tablets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3.0/4.0 Cannulated Drill Bit Recalled by Trilliant Surgical Ltd. Due to The...
The Issue: The cannulation of the 3.0/4.0 Cannulated Drill Bit inner diamter is too...
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: 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.
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: 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: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....
The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Discovery LS Recalled by GE Healthcare Due to Potential for expulsion of...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Discovery ST 16 Recalled by GE Healthcare Due to Potential for expulsion...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Passive Biopsy Needle Kit Recalled by Medtronic Navigation, Inc....
The Issue: The adhesive between the sphere assembly and the biopsy needle shaft may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wall Chart for STERRAD 100NX System Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization PRoducts (ASP) is recalling the Wall Chart for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lightspeed 16 CT Recalled by GE Healthcare Due to Potential for expulsion of...
The Issue: Potential for expulsion of the Power Supply on Lightspeed CT scanner or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-¿release Tablets USP (SR) Recalled by Sun...
The Issue: Failed Dissolution Specification: During analysis of the 18 month long term...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: glycopyrrolate Recalled by Pharmedium Services, LLC Due to Stability Data...
The Issue: Stability Data Does Not Support Expiry: potential loss of potency in drugs...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.