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. 2,519 recalls have been distributed to Hawaii in the last 12 months.
Showing 11341–11360 of 27,645 recalls
Recalled Item: Alaris Auto ID Module Model 8600 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris SpO2 Module Model 8210 and Model 8220 Recalled by CareFusion 303,...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DCA Vantage Handheld Barcode Scanner - Zebra Model - Model Recalled by...
The Issue: If DCA Vantage Analyzer is configured to run Code 39 with check digit, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8000 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Module Model 8120 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8000 modular infusion pump and monitoring system...
The Issue: If one or more screws or washers are loose or missing causing the battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Module Model 8110 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pleur-Evac Adult-Ped Wet Recalled by TELEFLEX MEDICAL INC Due to Potential...
The Issue: Potential for sterile packaging to be compromised¿
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressa Bed Recalled by Hill-Rom, Inc. Due to Affected beds may have...
The Issue: Affected beds may have screws installed that do not meet material tensile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearPro Trach T-Piece Closed Suction Catheter Recalled by Medline...
The Issue: There are reports of the suction catheter coming apart from the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centrella Smart+ Bed Recalled by Hill-Rom, Inc. Due to Affected beds may...
The Issue: Affected beds may have screws installed that do not meet material tensile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearPro T-Piece Closed Suction Catheter Recalled by Medline Industries Inc...
The Issue: There are reports of the suction catheter coming apart from the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX800 patient monitor Recalled by Philips North America, LLC Due...
The Issue: Some Intellivue MX700/MX800 Patient Monitors were delivered with defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX700 patient monitor Recalled by Philips North America, LLC Due...
The Issue: Some Intellivue MX700/MX800 Patient Monitors were delivered with defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERI-LOC TARGETER 4.5MM DISTAL FEMUR Recalled by Smith & Nephew, Inc. Due to...
The Issue: The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PVA Recalled by Precision Valve & Automation,Inc Due to While operating the...
The Issue: While operating the machine in "Run" mode an unexcepted event may occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOSS DeBakey "Gator-Grip" Needle Holder 2 mm tip Recalled by Boss...
The Issue: The tungsten carbide plate, which is intended to hold the sewing needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase Assay: Lipase Colorimetric R2 Substrate - Product Usage:...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase Assay: Lipase Colorimetric R1 Buffer - Product Usage: Recalled...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipase Assay: Lipase Colorimetric Reagent - Product Usage: A Recalled...
The Issue: Randox have confirmed imprecision of quality control and patient samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.