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. 2,544 recalls have been distributed to Hawaii in the last 12 months.
Showing 8341–8360 of 47,764 recalls
Recalled Item: Femoral Resurfacing Cup - (xx)MM Recalled by Synovo Production Due to...
The Issue: Medical device components were marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACETABULAR FIXATION CUP Recalled by Synovo Production Due to Medical device...
The Issue: Medical device components were marketed without FDA clearance and without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACETABULAR BEARING (xx)MM I.D X (xx) O.D. UHMWPE 1020 Recalled by Synovo...
The Issue: Medical device components were marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs...
The Issue: Weld protrusion/physical gap between the housing and pack cover, may exceed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) STURDI STRAINER TRAY STANDARD...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) CATH ANGIOGRAPHY DRAPE PACK...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) OPEN HEART TRACECART Recalled...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) PELVIC EXAM TRAY Recalled by...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom medical procedure packs labeled as: a) STANDARD OB PACK ASCENSION WI...
The Issue: The outer package seal could be open, or compromised which affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .14.800 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...
The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .14.500 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...
The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscope Reprocessor OER-Mini-For use in cleaning and high-level...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheal Intubation Fiberscope OLYMPUS LF-P- To be used with an Recalled by...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscope Reprocessor OER-Elite-For use in cleaning and high-level...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VISERA Tracheal Intubation Videoscope OLYMPUS LF Type V- For airway Recalled...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Endoscope Reprocessor OER-Pro-For use in cleaning and high-level...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed 14Fr Low Profile Introducer Set Recalled by Abiomed, Inc. Due to...
The Issue: There was one complaint that the sidearm of the device detached during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: 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: Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be Recalled...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.