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. 2,386 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,386 in last 12 months

Showing 2452124540 of 47,764 recalls

DrugJuly 5, 2018· Teva Pharmaceuticals USA

Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities and Degradation Specifications and Subpotent Drug:...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2018· Medgyn Products, Inc.

Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by Medgyn Products, Inc. Due...

The Issue: CGMP Deviations: The manufacturer of this product recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2018· Abbott Vascular

Recalled Item: PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended Recalled...

The Issue: Incorrect expiration being entered for one lot.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2018· ConvaTec, Inc

Recalled Item: AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device Recalled...

The Issue: Bubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2018· Radiometer America Inc

Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...

The Issue: The analyzer software may cause a mis-match of patient demographics and test...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Hudson Scientific LLC

Recalled Item: iTOVi Tracker/Scanner Recalled by Hudson Scientific LLC Due to The device...

The Issue: The device and its accessories may not have been manufactured according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Water Pik, Inc.

Recalled Item: Waterpik Sonic-Fusion Professional Recalled by Water Pik, Inc. Due to...

The Issue: Charging base may overheat with localized melting and sparking, possibly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2018· Cypress Medical Products LLC

Recalled Item: Powder Free Vinyl Exam Gloves Recalled by Cypress Medical Products LLC Due...

The Issue: The firm is recalling one lot of McKesson Powder Free Vinyl Exam Gloves...

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

Class II — Potential Health HazardOngoing
DrugJuly 2, 2018· AuroMedics Pharma LLC

Recalled Item: Piperacillin and Tazobactam for Injection USP 3.375 grams per vial Recalled...

The Issue: Presence of Particulate Matter: identified as glass and silicone material

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 29, 2018· Fagron Compounding Services LLC dba Fagron Sterile Services

Recalled Item: Neostigmine Methylsulfate Injection Solution Recalled by Fagron Compounding...

The Issue: Labeling: Label Error on Declared Strength: syringes of Neostigmine...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 29, 2018· Fagron Compounding Services LLC dba Fagron Sterile Services

Recalled Item: Neostigmine Methylsulfate Injection Solution Recalled by Fagron Compounding...

The Issue: Labeling: Label Error on Declared Strength: syringes of Neostigmine...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer (SMN 11066000). The Atellica" Solution is Recalled...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Quasar Bio-Tech, Inc.

Recalled Item: Pure Rayz Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not receive...

The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation stand-alone software treatment planning system Recalled by...

The Issue: If the beam model has a highly asymmetric primary source, it is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Additional (SMN 11069004). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Connect (SMN 11069018). The Atellica" Solution is...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer (SMN 11066001). The Atellica" Solution is Recalled...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer (SMN 11067000) . The Atellica" Solution Recalled by...

The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: 3D V Recalled by Siemens Medical Solutions USA, Inc Due to In rare cases of...

The Issue: In rare cases of insufficient maintenance or high clinical workload, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: 3D TOP Ceiling Stand Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: In rare cases of insufficient maintenance or high clinical workload, the...

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

Class II — Potential Health HazardOngoing