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. 2,386 recalls have been distributed to Hawaii in the last 12 months.
Showing 23681–23700 of 27,645 recalls
Recalled Item: VerSys¿ Hip System Recalled by Zimmer, Inc. Due to During routine...
The Issue: During routine inspection, beaded hip stem forgings received from supplier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...
The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon CUSTOM-PAK containing Anterior Chamber Cannula 27G Component Part...
The Issue: Alcon CUSTOM-PAK which is supposed to contain a 27G Anterior Chamber Cannula...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual Resuscitator Bag Series: AF1000 Recalled by Ventlab LLC Due to The...
The Issue: The pop-off valve in the defective devices remain open and a squeeze of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GYC-1000 Green Laser Photocoagulator system The Nidek Green Laser...
The Issue: Laser Aperture label was not applied to certain GYC-1000 Green Laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR systems: Ingenia HA FLEX TRAK Trolley (for Ingenia Recalled by...
The Issue: Ingenia customers have experienced clamping of the foot under the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo RT Dosimetrist 2.7 system Product Usage: The intended Recalled...
The Issue: An update to the Virtual Simulation software of the syngo RT Dosimetrist is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes B37 Replacement Screws. M3.5 Screw for insertion handle guide/aiming...
The Issue: All lots of B37 Replacement Screws are being recalled due to potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa" Flu A/B & RSV Direct Recalled by Focus Diagnostics Inc Due to...
The Issue: Focus Diagnostics is providing an urgent safety notice for a correction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISCOVERY ELBOW prosthesis Recalled by Biomet, Inc. Due to Surface finish is...
The Issue: Surface finish is different than specified. The implant has 30 grit blast on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T Recalled...
The Issue: Ingenia customers have experienced clamping of the foot under the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Recalled by Ebi, Llc Due to The Cypher MIS Screw Inserter may...
The Issue: The Cypher MIS Screw Inserter may exhibit an increased rate of instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.