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. 2,287 recalls have been distributed to Hawaii in the last 12 months.
Showing 44741–44760 of 47,764 recalls
Recalled Item: LeMaitre Stent Guide: 1102-00 (100 strips) Recalled by LeMaitre Vascular,...
The Issue: Devices were not sealed correctly during the manufacturing process, and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...
The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: Pump shutting off during use without warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: Pump shutting off during use without warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...
The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glow 'N Tell 20 cm Tape: 1100-00 (100 strips) Recalled by LeMaitre Vascular,...
The Issue: Devices were not sealed correctly during the manufacturing process, and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Ojemann Cortical Stimulator Recalled by Integra Burlington MA, Inc....
The Issue: If the headphone jack is in use during a surgical procedure with the OCS2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "Well at Wallgreens" Regular Strength Antacid Liquid...
The Issue: Microbial Contamination of Non-Sterile Products: Lot in question had an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lessina(R) (Levonorgestrel and ethinyl estradiol tablets Recalled by Teva...
The Issue: Failed Impurity/Degradation Specification; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Errin (norethindrone tablets Recalled by Teva Pharmaceuticals USA, Inc. Due...
The Issue: Failed Impurity/Degradation Specification; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Junel(TM) Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets...
The Issue: Failed Impurity/Degradation Specification; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camila (norethindrone tablets Recalled by Teva Pharmaceuticals USA, Inc. Due...
The Issue: Failed Impurity/Degradation Specification; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Jolessa(R) (levonorgestrel/ethinyl estradiol tablets Recalled by Teva...
The Issue: Failed Impurity/Degradation Specification; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Balziva(TM) (norethindrone and ethinyl estradiol tablets Recalled by Teva...
The Issue: Failed Impurity/Degradation Specification; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system...
The Issue: There was an occurrence where the patient case data did not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: The proximal and distal pressure sensor calibration can drift resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: The proximal and distal pressure sensor calibration can drift resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS3000 USER MANUAL for Intuitive Surgical da Vinci Si Surgical Recalled by...
The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS2000 USER MANUAL for Intuitive Surgical da Vinci S Surgical System...
The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.