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. 2,391 recalls have been distributed to Hawaii in the last 12 months.
Showing 23081–23100 of 47,764 recalls
Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Dr. Reddy's...
The Issue: Failed stability specifications - An out of specification result was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clozapine Orally Disintegrating Tablets Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Disintegration Specifications: Out-of-specification disintegration...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle...
The Issue: CGMP Deviations; rejected product was used to manufacture final bulk lot
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meropenem for Injection Recalled by Pfizer Inc. Due to Lack of assurance of...
The Issue: Lack of assurance of sterility: loss of container integrity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Single-Use Biopsy Forceps Recalled by Micro-Tech (Nanjing) Co., Ltd. Due to...
The Issue: Single-Use Biopsy Forceps box contains incorrect product, instead it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid IABP Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: There is a potential for interruption and/or inability to start therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IABP Recalled by Maquet Datascope Corp - Cardiac Assist...
The Issue: There is a potential for interruption and/or inability to start therapy to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AS-OBGYN Information System version 7.824.x Recalled by AS Software, Inc....
The Issue: Any change made to current ultrasound machine software or hardware upgrades,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...
The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elelyso (taliglucerase alfa) for injection Recalled by Pfizer Inc. Due to...
The Issue: Lack of assurance of sterility -Reports of loose metal ferrule crimps on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/ degradation specifications: Product is Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/ degradation specifications: Product is Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Altavera Levonorgestrel and Ethinyl Estradiol Tablets Recalled by Xiromed...
The Issue: Labeling: Not Elsewhere Classified: mislabeling of the Altavera generic name...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...
The Issue: Cross contamination may have occurred between wells for the reagent pack. As...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...
The Issue: Software Update: External USB Drive performance and its impact on Graphic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic...
The Issue: O-arm 02 Imaging Systems correction to software version 4.1.0; new version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Agilis Steerable Introducer: indicated for introducing various...
The Issue: Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NucliSENS¿ Magnetic Extraction Reagents Recalled by BioMerieux SA Due to...
The Issue: Data loggers showed that one shipment to the United States experienced low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301 Recalled by...
The Issue: The power supply unit for the printer used with the device can potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: treatNOW ABILIFY (aripiprazole) / ABILIFY MAINTENA 400-mg (aripiprazole) for...
The Issue: Labeling Not Elsewhere Classified: Physician sample kits/cartons of treatNOW...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.