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. 2,350 recalls have been distributed to Hawaii in the last 12 months.
Showing 35341–35360 of 47,764 recalls
Recalled Item: Mahurkar" Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraPrep Surgical Solution Iodine Povacrylex (0.7% Available Iodine) and...
The Issue: Chemical contamination: Product may be contaminated with a toxic compound.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KABOOM action strips Recalled by Blue Square Market, Inc. Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared Sulfoaildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LiDa DAIDAIHUA (also packaged as LiDa DAIDAIHUAJIAONANG) Recalled by Blue...
The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared Sibutramine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Topicort (desoximetasone) Topical Spray Recalled by Taro Pharmaceuticals,...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biomet Parsippany Recalled by Biomet Spine, LLC Due to Mislabeling
The Issue: Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology...
The Issue: The Leica ASP200S/ASP300S Tissue Processor have an incorrect internal wiring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to A software fix...
The Issue: A software fix has been released to prevent automatic movement resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy Recalled by...
The Issue: The neoBLUE Instruction For Use (IFU) and Service Manuals for the neoBLUE 3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NebuTech Nebulizer Recalled by Salter Labs Due to The Inspiratory valve cap...
The Issue: The Inspiratory valve cap on the nebulizer reservoir tower may be loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angiographic Injector. Medrad Mark 7 Arterion Injection System Recalled by...
The Issue: Software Version SW 005.006_SH, resulted in the removal of purge enforcement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROFEMUR PLUS CoCr MODULAR NECK Recalled by MicroPort Orthopedics, Inc. Due...
The Issue: Unexpected rate of postoperative fractures resulting in the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Formula IM packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula E packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Expello-C packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Golden Seal Extract packaged in 1 FL OZ (29mL) droppers. HoneyCombs...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula L packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Formula KB packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.