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. 2,582 recalls have been distributed to Hawaii in the last 12 months.
Showing 3401–3420 of 47,764 recalls
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PCR Cartridges used with MAX System. Model Number: 437519 Recalled by...
The Issue: Potential for signal drift in specific lots of BD PCR Cartridges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS XT 7600 Integrated System Recalled...
The Issue: The VITROS XT 7600 Integrated System software versions 3.8.0 may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog...
The Issue: The VITROS 5600 Integrated System software versions 3.8.0 may not correctly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 3600 Immunodiagnostic System...
The Issue: The VITROS 3600 Immunodiagnostic System software versions 3.8.0 may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bodor P and C series laser cutting machines Recalled by Jinan Bodor Cnc...
The Issue: Non-compliant laser products
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...
The Issue: Due to an increase in complaints for pitch cable failures related to forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...
The Issue: Due to an increase in complaints for pitch cable failures related to forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope - - Optical Biopsy and Grasping Forceps Recalled by...
The Issue: Due to failure of manual cleaning validation, biopsy and grasping forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Systane Lubricant Eye Drops Recalled by Alcon Research LLC Due to Non-Sterility
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colchicine Capsules 0.6 mg Recalled by Granules Pharmaceuticals Inc. Due to...
The Issue: Failed Dissolution Specifications: Out of specification observed during the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: medroxyPROGESTERone Acetate Injectable Suspension Recalled by Eugia US LLC...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% Moisturizing...
The Issue: LABELING: LABEL MIX-UP
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.