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. 2,375 recalls have been distributed to Hawaii in the last 12 months.
Showing 25681–25700 of 27,645 recalls
Recalled Item: INSTAT - Agent Recalled by Integra LifeSciences Corporation Due to Due to...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter for difficult...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraGen XS Dural Regeneration Matrix DuraGen XS Dural Regenerative Matrix...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set Recalled by...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuraWrap Nerve Protector NeuraWrap Nerve Protector is indicated for the...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CollaPlug Absorbable Collagen Wound Dressing for Dental Surgery The...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro¿ Single Stage Embryo Replacement Catheter Product Code:...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOTECH Endoscope Cleaner and Reprocessor System Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HCS3011 AV Loop Kit For use with Transonic CO status System Only Recalled by...
The Issue: Transonic Systems Inc. have received complaints of blood leakage involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter with Obturator...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OraTape Absorbable Collagen Wound Dressing for Dental Surgery The Absorbable...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Layershield Adhesion Barrier Matrix Layershield Adhesion Barrier Matrix is...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wallace Sure-Pro Ultra¿ Embryo Replacement Catheter with Obturator Product...
The Issue: Unable to pass catheter through outer sheath during embryo transfer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity 1.1. Integrity is the interface and control software for Recalled...
The Issue: The problem is that the "static tolerances" from the calibration files...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The CEP 8 SpectrumGreen (SG) ASR Probe Kit Recalled by Abbott Molecular Due...
The Issue: 20 kits of CEP 8 SG ASR Probe (list 06J37-018, lot 440023), contained Vysis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helitene Absorbable Collagen Hemostatic Sponge Helitene is indicated in...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Spine ISSYS LP Inverted Screw System. 8.5MM X 45 Recalled by Custom...
The Issue: On March 28, 2013, Custom Spine, Inc. issued a minor removal of a lot of 18...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMend¿ Extend" Absorbable Collagen Membrane BioMend¿ Extend" Absorbable...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraGen Plus Dural Regeneration Matrix DuraGen Plus Adhesion Barrier Matrix...
The Issue: Due to the process deviation, product lots in question may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A) Product Code 2N8371: Non-DEHP Y-Type Catheter Extension Set Kit Recalled...
The Issue: Customers have reported that when separating an individual package from its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.