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 27421–27440 of 47,764 recalls
Recalled Item: EMBLEM S-ICD Recalled by Boston Scientific Corporation Due to The device can...
The Issue: The device can deliver an atypical amount of energy due to memory corruption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Instrument Set EM ENT Recalled by Medtronic Navigation, Inc. Due...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic ENT Prgm 9734636 Add Fusion Nav AxiEM Recalled by Medtronic...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Suction 9734308 Small AxiEM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg 30 tablets per...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and...
The Issue: Presence of Foreign Substance: possibility of the presence of metal in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Obagi-C Rx System C-Therapy Night Cream Recalled by Valeant Pharmaceuticals...
The Issue: Labeling: Incorrect or Missing Package Insert - Obagi-C Rx System C-Therapy...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Converters(R) Under Buttocks Drape with Fluid Control Pouch II Recalled by...
The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Converters(R) Tiburon(R) Arthroscopy Drape Recalled by Cardinal Health 200,...
The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.