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. 1,077 recalls have been distributed to Hawaii in the last 12 months.
Showing 8481–8500 of 47,764 recalls
Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexi-Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Recalled by...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCHELIT Safety Clear Tracheal Tube Recalled by TELEFLEX LLC Due to Reports...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal Murphy Eye Recalled by TELEFLEX LLC Due to...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enterade Advanced Oncology Formula Recalled by ENTRINSIC HEALTH SOLUTION INC...
The Issue: Potential for the product to develop mold and spoil.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Travoprost Ophthalmic Solution Recalled by Golden State Medical Supply Inc....
The Issue: Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EliA GBM Wells Recalled by Phadia Ab Due to Complaints that specific samples...
The Issue: Complaints that specific samples produced false positive EliA GBM results. A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-PRO 2- A powered ambulance cot that consists of a platform Recalled by...
The Issue: Base leg assembly may bend and result in difficulty engaging/disengaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RET Proximal Probe. Used in Fluorescence in situ hybridization (FISH)...
The Issue: DNAs used during the manufacture of two affected models were accidentally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuMoDx Cartridge-used for extraction Recalled by NeuMoDx Molecular Inc Due...
The Issue: Top label on some of the NeuMoDx cartridges within these lots may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RET Distal Probe. Used in Fluorescence in situ hybridization (FISH) Recalled...
The Issue: DNAs used during the manufacture of two affected models were accidentally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revize Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revize-X Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.