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. 2,375 recalls have been distributed to Hawaii in the last 12 months.
Showing 27321–27340 of 27,645 recalls
Recalled Item: ***NOVATION MODULAR DRILL BIT LENGTH: 30mm Recalled by Exactech, Inc. Due to...
The Issue: Exactech Inc. of Gainesville, FL is recalling their Novation Modular Drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VMX Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware of...
The Issue: GE Healthcare has become aware of an issue associated with the base casting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER PrepPlus Recalled by Beckman Coulter Inc. Due to The recall was...
The Issue: The recall was initiated because Beckman Coulter has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEE-1000A Neuromaster Recalled by Nihon Kohden America Inc Due to The...
The Issue: The MEE-1000A Neuromaster had defective printed circuit boards (PCBs). Gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker AVS Navigator Trials 6mm-15mm Manufactured by: Stryker Spine SAS...
The Issue: Beginning in February 2011, Stryker Spine began receiving reports related to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viva - JR Recalled by Vital Scientific N.V. Due to The action was initiated...
The Issue: The action was initiated due power supply failure. During a power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viva-E Recalled by Vital Scientific N.V. Due to The action was initiated due...
The Issue: The action was initiated due power supply failure. During a power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action was initiated due...
The Issue: The action was initiated due power supply failure. During a power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Selectra ProS Analyzer Recalled by Vital Scientific N.V. Due to The action...
The Issue: The action was initiated due power supply failure. During a power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Selectra ProM Analyzer Recalled by Vital Scientific N.V. Due to The action...
The Issue: The action was initiated due power supply failure. During a power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "***Electric Systems Foot Control****Rx Only***" Product Usage: Cutting and...
The Issue: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "***Electric Systems Foot Control with Direction and Irrigation***Rx...
The Issue: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "***Electric Systems Foot Control with Direction Only***Rx Only***" Product...
The Issue: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling the foot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 518 Vascular Self Expanding Stent The Zilver Vascular Stent Recalled...
The Issue: Cook Ireland received a product complaint from Japan on December 22nd, 2011....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KRD1 PedFuse Rods Recalled by SpineFrontier, Inc. Due to One of the rods in...
The Issue: One of the rods in each of two test constructs did not meet fatigue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Accolade Offset Rasp Handle Howmedica Osteonics...
The Issue: Stryker Orthopaedics has become aware of the potential for the above noted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker Orthopaedics has become aware of the potential for cracking of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpineFrontier S-Lift Lock Shaft Inserter Recalled by SpineFrontier, Inc. Due...
The Issue: It has been verified through field use that there are two possible breakages...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2100 IQ Recalled by GE Healthcare, LLC Due to While...
The Issue: While performing a fluoroscopic examination on the GE Innova systems, there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare innova 3131-IQ Mobile X-ray system. The innova systems...
The Issue: It was discovered of a potential failure of the spectral filter mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.