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. 2,391 recalls have been distributed to Hawaii in the last 12 months.
Showing 22441–22460 of 27,645 recalls
Recalled Item: The I-Cart is used to store Recalled by Richard Wolf Medical Instruments...
The Issue: The transformers installed on carts used for Richard Wolf medical video...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Integrated APD Set with Cassette 3-Prong Recalled by Baxter...
The Issue: Baxter is issuing a recall for one lot of Integrated Automated Peritoneal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Brilliance and Ingenuity Computed Tomography X-ray systems Recalled...
The Issue: Improper assembly of the vertical motor/brake system may lead to uncommanded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS3000 Vision Side Cart (VSC) used in conjunction with the Recalled by...
The Issue: Intuitive Surgical is initiating a voluntary correction related to da Vinci...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INRatio 2 Monitors - 0200431 Alere INRatio 2 PT/INR Professional Recalled by...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio PT/INR Test Strips Recalled by Alere San Diego, Inc. Due to In...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INRatio Monitors - 0100004 Alere INRatio PT/INR System Professional -...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G- Series Beds Recalled by Invacare Corporation Due to Invacare identified...
The Issue: Invacare identified that the rail mounting bracket on the G29 full length...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle Recalled by...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensei X Robotic Catheter System Recalled by Hansen Medical Inc Due to The...
The Issue: The Set Up Joint subassembly of the Sensei X Robotic Catheter System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Recalled by Zimmer...
The Issue: Zimmer received a single complaint wherein a Trilogy® Fiber Metal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The...
The Issue: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriaDyne Proventa Critical Care Therapy System. The TriaDyne Proventa...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RotoRest Delta Advanced Therapy System. The RotoRest Delta Advanced Kinetic...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotoprone Therapy System. The Rotoprone Therapy System is an advanced...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing...
The Issue: The firm discovered that during the use of these defibrillation electrodes a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTH8 Rotor Recalled by Iris Diagnostics Due to Iris International is...
The Issue: Iris International is recalling the RTH8 Rotor used in the StatSpin Express...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ferno Model 35X PROFlexx Stretchers Recalled by Ferno-Washington Inc Due to...
The Issue: The wheel castor assemblies may be loosening on the stretchers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating...
The Issue: The manufacturing dates and expiration dates were transposed on the Tyvek label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.