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. 2,372 recalls have been distributed to Hawaii in the last 12 months.
Showing 31381–31400 of 47,764 recalls
Recalled Item: Senexon Liquid (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...
The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ninjacof-A (acetaminophen Recalled by Pharmatech LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Senna Syrup (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...
The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD 23 G x .75 in. BD Vacutainer¿ Push Button Recalled by Becton Dickinson &...
The Issue: BD has received multiple reports of units associated with the 23 G x .75 in....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Permits access...
The Issue: Shipping carton labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Calibrator U Recalled by Siemens Healthcare...
The Issue: Failure of analytical sensitivity with Calibrator U kit lots ending in 63...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Module Model 8110 with software version 9.15 The Recalled by...
The Issue: A software anomaly with the Alaris Syringe module software version 9.15 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Line Catheterization Kit with Sharps Safety Features Permits access...
The Issue: Shipping carton labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Claravis (isotretinoin capsules USP) Recalled by Teva North America Due to...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...
The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.x picture archiving and communication system Syngo.x is a software...
The Issue: Software error. Incorrect values for the volume calculation from a freehand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via picture archiving and communication system Syngo via is a Recalled...
The Issue: Software error. Incorrect values for the volume calculation from a freehand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nylon Surgical Suture for human use and vet use Recalled by Riverpoint...
The Issue: Nylon Surgical Sutures are recalled because the seals may become open during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam and Symbia E gamma camera systems with patient beds Recalled by...
The Issue: "We have received reports of patients hair being caught in the e.cam and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polypropylene Surgical Sutures Recalled by Riverpoint Medical, LLC Due to...
The Issue: Polypropylene Surgical Sutures are recalled because the seals may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bupivacaine Hydrochloride Inj. Recalled by Hospira Inc., A Pfizer Company...
The Issue: Presence of particulate matter: Confirmed customer report for the presence...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablets Recalled by Amerisource...
The Issue: Failed dissolution specifications - the out of specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: O Organics Vegetable Tray Recalled by Mann Packing Company, Inc. Due to...
The Issue: Incorrect ingredient label was attached to 18 oz. O Organics vegetable Trays...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MISAGO RX Self Expanding Peripheral Stem Recalled by Terumo Medical Corp Due...
The Issue: During recent routine testing, the MISAGO Peripheral Stent was found not to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.