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 26781–26800 of 27,645 recalls
Recalled Item: Visual-ICE¿ Cryoablation System Recalled by Galil Medical, Inc. Due to Galil...
The Issue: Galil Medical is recalling a number of Visual Ice Cryoablation Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Monitor B850 Product Usage: The CARESCAPE TM Monitor B850 Recalled...
The Issue: GE Healthcare become aware of 4 potential issues associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 Recalled by...
The Issue: Abbott Point of Care (APOC) has determined that for the Cliniqa Liquid QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to There is a...
The Issue: There is a potential malfunction in which a miscalculation occurs for images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Imaging XS. Radiological image processing system. Recalled by Siemens...
The Issue: There is a potential malfunction when using syngo Imaging XS, version VA70A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00-4309-029-01 - Trabecular Metal Reverse Shoulder Liner 36 mm 65¿¿ Recalled...
The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiley Reusable Cannula Low Pressure Cuffed Tracheostomy Tubes Recalled by...
The Issue: Covidien is recalling certain cuffed Shiley tracheostomy tubes due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trabecular Metal Reverse Shoulder Liner 40mm Recalled by Zimmer, Inc. Due to...
The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00-4309-029-00- Trabecular Metal Reverse Shoulder Liner 36mm Recalled by...
The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00-4309-028-01 - Trabecular Metal Reverse Shoulder Liner 40mm 65¿ Neck...
The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Syphilis (SYPH) Assay Recalled by Siemens Healthcare...
The Issue: Syphilis Assay Interference with HBsAg Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conformis iTotal CR-Cruciate Retaining Knee Replacement System Model...
The Issue: Addendum Labeling iTotal CR Surgical Technique with Detailed Instructions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RF Cannula Recalled by Stryker Instruments Div. of Stryker Corporation Due...
The Issue: Stryker has received 6 complaints that the 5mm needle was placed in 10 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension(R) Reagent Management System (RMS) - Power Cord. The Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed that partial insertion of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RF Cannula Recalled by Stryker Instruments Div. of Stryker Corporation Due...
The Issue: Stryker has received 6 complaints that the 5mm needle was placed in 10 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IR1200 Recalled by Animas Corporation Due to Wear of the keypad that may...
The Issue: Wear of the keypad that may lead to damage such as tearing or peeling of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: djo surgical Screw 6.5 mm Recalled by Encore Medical, Lp Due to Mislabeling
The Issue: One lot of the 010-55-030, 6.5 mm Cancellous Bone Screw was recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The COBAS INTEGRA 400/400 plus system (software version 3.4) is Recalled by...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MagNA Pure 96 System (versions 1.0 and 2.0) is Recalled by Roche...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DataCare POC is an information management system that provides Recalled by...
The Issue: Roche Molecular Systems, Inc. has become aware of a device-associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.