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. 2,512 recalls have been distributed to Hawaii in the last 12 months.
Showing 11881–11900 of 47,764 recalls
Recalled Item: Nitrofurantoin Capsules Recalled by American Health Packaging Due to Failed...
The Issue: Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sirolimus Oral Solution Recalled by Apotex Corp. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Sirolimus Oral Solution recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Keto Living Sugar Control Recalled by Natural Organics, Inc. Due to...
The Issue: Contains undeclared wheat (gluten) in product labeled "gluten free"
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MVASI (bevacizumab-awwb) Recalled by Amgen, Inc. Due to Defective container:...
The Issue: Defective container: loose crimp defect, potential loss of container integrity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablet Recalled by SUN...
The Issue: Presence Of Foreign Substance: Customer complaint for the presence of dark,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablet Recalled by SUN...
The Issue: Presence Of Foreign Substance: Customer complaint for the presence of dark,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adult Cap-ONE Biteblock The cap-ONE Biteblock is intended Recalled by Nihon...
The Issue: Due to products being shipped/distributed to customers after the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERGARD Woven Vascular Graft is a woven polyester graft coated Recalled by...
The Issue: Mislabeled: Product labeled as Intergard Woven Straight graft , D: 8 mm, L:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM CONTACT EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Enterprise Web Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Cardiology CA1000 Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS RA1000 Recalled by GE Healthcare, LLC Due to Potential for...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIRMap" Catheter Recalled by Abbott Due to Incorrect product labeling.
The Issue: Incorrect product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Radiology RA600 Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Zero Footprint Client Recalled by GE Healthcare,...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELITE GRAPE GUM WITH SUGAR NET WT. 2.32 (66 g) Recalled by ELITE...
The Issue: Potential contamination with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ELITE WHITE CHOCOLATE BAR & 815871012799. Net Wt. 3.53 Recalled by ELITE...
The Issue: Potential contamination with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ELITE PESEK ZMAN WAFER ROLL NET WT. 1.4 oz (40g) Recalled by ELITE...
The Issue: Potential contamination with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.