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 25821–25840 of 27,645 recalls
Recalled Item: The LifeCare PCA Plus II infusion pump system is designed for safe Recalled...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare PCA Infusion System with Hospira MedNet Software Recalled by...
The Issue: Screw rotation error occurring when the pump detects a mismatch between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET CARDIOHELP Support System: CARDIOHELP-I Software (up to version...
The Issue: It has come to the attention of MAQUET that there have been episodes of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Getinge Group battery modules for use with Maquet SERVO-i Recalled by...
The Issue: When using the SERVO-i on battery power, in a very small number of cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent" irrigation tubing. Product Usage: The Torrent irrigation system...
The Issue: The firm was notified by their customers that there was a water leakage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Diagnostics Inc. MIcroScan MICroSTREP plus Type 1...
The Issue: Customer complaint investigation confirmed the issue of false skipped wells...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Inform II Blood Glucose Monitoring System bar code scanner....
The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Alere Cholestech LDX¿ high sensitivity C-Reactive Protein (hsCRP) Test...
The Issue: The Alere Cholestech LDX¿ hsCRP cassette (PN 12-807) may have increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...
The Issue: The recall was initiated because Carefusion has identified potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 with software version 9.12 Product Recalled by...
The Issue: The recall was initiated because Carefusion has received reports of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX ALT AST Test Cassette Recalled by Alere San Diego, Inc....
The Issue: The recall was initiated because Alere San Diego has an update for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS Pro meters (catalog number 05530199160)bar code scanner. Used...
The Issue: Roche investigation into complaints found Accu-Chek Inform II and CoaguChek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a...
The Issue: Unapproved medical device
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN (TM) L-P SCREW Recalled by Smith & Nephew Inc Due to One batch of 4.5...
The Issue: One batch of 4.5 mm diameter Trigen Low-Profile Bone Screws were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20-Pole Eco Cable Recalled by Biosense Webster, Inc. Due to Biosense is...
The Issue: Biosense is recalling the 20-Pole Eco Cable because it was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Inline Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntellVue Info Center iX 866023 Recalled by Philips Healthcare Inc....
The Issue: If a customer creates customized trend scales in the trend review tile and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1488 HD 3-Chip Camera Recalled by Stryker Endoscopy Due to In certain...
The Issue: In certain operating room environments, a colored screen image occurs with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 16 Multi-Slice CT Scanner System Recalled by Philips And Neusoft...
The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.