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. 1,027 recalls have been distributed to Hawaii in the last 12 months.
Showing 16221–16240 of 47,764 recalls
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 1 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HUMAN CHORIONIC GONADOTROPIN 6 Recalled by Complete Pharmacy and Medical...
The Issue: CGMP deviations: Lack of potency testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Scandonest 3% Plain (Mepivacaine Hydrochloride 3% without Vasoconstrictor)...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HLS Set Advanced Recalled by Maquet Cardiovascular Us Sales, Llc Due to The...
The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS Set Advanced Model Name: BEQ-HLS 5050 USA Recalled by Maquet...
The Issue: The HLS Set Advanced (disposable for Cardiohelp) is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haag Streit Surgical Floor stands FS 2-11 (. 615H511) Recalled by...
The Issue: Software error -Software 588 versions 2.0 to 3.3, movement of the focusing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Rod Cutter Recalled by Zimmer Biomet, Inc. Due to Device has the...
The Issue: Device has the potential for fracture during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Automation Solutions Recalled by Ortho-Clinical Diagnostics, Inc. Due...
The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System Recalled by Ortho-Clinical Diagnostics,...
The Issue: A software anomaly may cause an aliquoted sample to be labelled as the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 18.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 17.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 16.0MM REAMER HEAD FOR RIA 2 STERILE--Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 16.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 12.5MM REAMER HEAD FOR RIA 2 STERILE -Orthopedic Recalled by...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 12.0MM REAMER HEAD FOR RIA 2 STERILE -Orthopedic Recalled by...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 14.5MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 17.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The cobas z 480 analyzer including dedicated software for IVD Recalled by...
The Issue: Dirty Lens May Cause Invalid or False Positive Results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CM 50-001-01 Injectate Kit Recalled by Lidco Ltd Due to The expiration date...
The Issue: The expiration date on labeling is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 11.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual...
The Issue: RIA 2 reamer head breakage exceeds the expected occurrence rate resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.