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. 1,679 recalls have been distributed to Hawaii in the last 12 months.
Showing 43241–43260 of 47,764 recalls
Recalled Item: ADVIA 120 Hematology Analyzer Recalled by Siemens Healthcare Diagnostics Due...
The Issue: The ADVIA 120 optics cover or hood is located on the very top of the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSA Assays for use in the IMMULITE/IMMULITE 1000 Systems Analyzers Recalled...
The Issue: Customers complained of a positive bias in patient results on the IMMULITE/...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS zee and zeego x-ray Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens issued a customer safety advisory notice and field safety corrective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur HCY Diluent - 10mL Bottle Catalog number 09877493 (124533)...
The Issue: ADVIA Centaur Homocysteine dilution recovery on the diluent identified the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Flexi-Seal SIGNAL Fecal Management System Recalled by Convatec Inc....
The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Flexi-Seal SIGNAL + Recalled by Convatec Inc. Due to ConvaTec...
The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Latanoprost Ophthalmic Solution Recalled by Apotex Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: Failed at expiry for Preservative...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin Injection Recalled by Fresenius Kabi USA, LLC Due to Subpotent...
The Issue: Subpotent Drug; 15-month stability test station
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-852-000 (Console 230V) Product...
The Issue: A supplied component exhibiting corrosion was built into the power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-851-000(Console 100V) Product...
The Issue: A supplied component exhibiting corrosion was built into the power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SC2316 Recalled by Stelkast Co Due to The firm became aware of an incident...
The Issue: The firm became aware of an incident relating to a breach of sterility in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonopet Ultrasonic Aspirator Console (Console 110V with Pedal & Pole)...
The Issue: A supplied component exhibiting corrosion was built into the power supply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Matrix 5.5.mm Left and Right Coronal Bender Product Usage: Recalled...
The Issue: A complaint was received of the tips of the Matrix 5.5.mm Left and Right...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-2.5 mL LeGoo with 1 Cannula Pouch Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MHI-TM2000 Linear Accelerator System Recalled by MITSUBISHI HEAVY...
The Issue: Software anomaly: Mitsubishi Heavy Industries, Ltd. became aware of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.5 mL LeGoo w/ no Cannula Product...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Internal Vessel Occluder .25mL Product Number: 10-0025 LeGoo is...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Internal Vessel Occluder 2.5mL Product Number: 10-0250 LeGoo is...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo Internal Vessel Occluder 10mL Product Number: 10-1000 LeGoo is...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeGoo¿ Endovascular Occlusion Gel-1.0 mL LeGoo with 3 Cannula Pouch Recalled...
The Issue: Product contains particulates (fibers)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.