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 24701–24720 of 27,645 recalls
Recalled Item: Stryker Orthopaedics Ball Impactor Tip Product Usage: Used for ADM Recalled...
The Issue: Stryker has received complaints associated with cracks and/or fracture of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic RestoreUltra Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic notified customers regarding Loss of Stimulation of specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Zero-P VA Implant 7 MM Height Parallel Sterile The Recalled by...
The Issue: A potential non conformance was identified with the Zero-P VA plate where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Activa PC Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic notified customers regarding over stimulation or stimulation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adjustable Gastric Band Recalled by Ethicon Endo-Surgery Inc Due to During...
The Issue: During aging studies, the firm determined that the gastric belts were unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic RestoreUltra Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic notified customers regarding over stimulation or stimulation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine...
The Issue: Custom Procedural Trays/Kits contain 1% Lidocaine HCl injection which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Movita 603x/DVE 803x Ceiling Supply Unit. It is intended Recalled by...
The Issue: Cases were encountered with the Draeger Movita 603x/DVE 803x Ceiling Supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adjustable Gastric Band Recalled by Ethicon Endo-Surgery Inc Due to During...
The Issue: During aging studies, the firm determined that the gastric belts were unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Activa PC Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic notified customers regarding Loss of Stimulation of specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod Insulin Management System Starter Kit Recalled by Insulet...
The Issue: Alcohol Prep Pads contained within the kit are not properly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod Insulin Management Product Demonstration Kit Recalled by Insulet...
The Issue: Alcohol Prep Pads contained within the kit are not properly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TB-0545PC: THUNDERBEAT 5 mm Recalled by Olympus America Inc. Due to...
The Issue: Complaints of damage to various models of Thunderbeat Hand Instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B. Braun Introcan Safety IV Catheter PUR 24G Recalled by B. Braun Medical,...
The Issue: One lot of Introcan Safety IV Catheters may not contain the anti-needlestick...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis OPTEASE Vena Cava Filter Is indicated for use in Recalled by Cordis...
The Issue: Cordis identified a printing error on one unit of the Optease Vena Cava...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breeze C Scooter is a motorized electric scooter for elderly Recalled by...
The Issue: Breeze C Scooter, motorized 3-wheeled electric scooter for elderly people,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-C2 Ventilator: Manufactured by Hamilton Medical AG CH-7402 Bonaduz...
The Issue: Manufacturer defined limits for improperly functioning loudspeakers of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Recalled by Baxter Healthcare Corp. Due to Incomplete foil seal on...
The Issue: Incomplete foil seal on one lot of sterile product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon Stratafix Symmetric PDS Plus Knotless Tissue Control Device Ethicon...
The Issue: Ethicon Stratafix Symmetric PDS Plus Knotless Tissue Control Device has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Soft Tissue Retractor Small Extendible Offset blade facilitates easy...
The Issue: The potential exists for the locking screw nut to break on the Soft Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.