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.

47,764 total recalls
2,375 in last 12 months

Showing 2600126020 of 47,764 recalls

DrugJanuary 19, 2018· Flawless Beauty LLC

Recalled Item: TAD Glutathione Whitening Kits lyophilized powder for injection Recalled by...

The Issue: Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2018· Flawless Beauty LLC

Recalled Item: Saluta Glutathione Whitening kits Recalled by Flawless Beauty LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2018· Flawless Beauty LLC

Recalled Item: Sterilized water for injections BP Recalled by Flawless Beauty LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2018· Flawless Beauty LLC

Recalled Item: Reiki Glutathione Whitening kits Recalled by Flawless Beauty LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 19, 2018· AMERICAN HEALTH PACKAGING

Recalled Item: Aripiprazole Tablets Recalled by AMERICAN HEALTH PACKAGING Due to CGMP...

The Issue: CGMP Deviations: lot made with active pharmaceutical ingredient that did not...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 18, 2018· Beckman Coulter Inc.

Recalled Item: AutoMate 2550 "High Speed" Catalog Number ODL25255 Recalled by Beckman...

The Issue: A misaligned pipette tip sensor poses the remote risk of cross-contamination...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJanuary 17, 2018· Magno Humphries Laboratories, Inc

Recalled Item: Senna Laxative (sennosides) tablets Recalled by Magno Humphries...

The Issue: Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R Recalled by...

The Issue: Potential breakage of the endoscope s insertion tube bending section during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno fiberscope URF-P6 Recalled by Olympus Corporation of the...

The Issue: Breakage of the endoscope's insertion tube bending section during surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2018· Olympus Corporation of the Americas

Recalled Item: Uretero-reno fiberscope URF-P6RP6 Recalled by Olympus Corporation of the...

The Issue: Breakage of the endoscope's insertion tube bending section during surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJanuary 16, 2018· Ottogi America Inc

Recalled Item: Ottogi Rice Cake Soup Recalled by Ottogi America Inc Due to Undeclared Milk

The Issue: Firm determined that their Rice Cake Soup has undeclared milk in the form of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 16, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: DOXOrubicin Hydrochloride Liposome Injection Recalled by Sun Pharmaceutical...

The Issue: Lack Of Assurance Of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2018· Fresenius Kabi USA, LLC

Recalled Item: Vecuronium bromide for Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Failed impurities/ degradation specifications: Out-of-specification (OOS)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodJanuary 15, 2018· Jarrow Formulas Inc

Recalled Item: Jarrow Formulas Liquid L-Carnitine Recalled by Jarrow Formulas Inc Due to A...

The Issue: A higher than normal micro result was found at the six month time point for...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 12, 2018· Manicaretti Inc

Recalled Item: IASA COLATURA DI ALICI DI CETARA ANCHOVY EXTRACT Recalled by Manicaretti Inc...

The Issue: Rapid Alert System for Food and Feed notification received from Italy...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 12, 2018· Cook Inc.

Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a...

The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Hill-Rom, Inc.

Recalled Item: Progressa Bed - AC-powered adjustable hospital bed Recalled by Hill-Rom,...

The Issue: A component used within the braking system may break resulting in one or...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Shimadzu Medical Systems

Recalled Item: Sonialvision Safire II Recalled by Shimadzu Medical Systems Due to When...

The Issue: When selecting serial radiography with a pulse rate of 7.5fps (including...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2018· Beckman Coulter Inc.

Recalled Item: COULTER EPICS XL Flow Cytometer COULTER EPICS XL-MCL Flow Cytometer Recalled...

The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 12, 2018· Beckman Coulter Inc.

Recalled Item: 1) Cytomics FC 500 With CXP Software BECKMAN COULTER 2) Recalled by Beckman...

The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing