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. 1,051 recalls have been distributed to Hawaii in the last 12 months.
Showing 14001–14020 of 47,764 recalls
Recalled Item: Arformoterol Tartrate Inhalation Solution 15 mcg*/2 mL For Oral Inhalation...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zonisamide Capsules USP 100 mg Rx Only Manufactured by: Glenmark Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Naproxen Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorzoxazone Tablets USP 750 mg 100 Tablets Rx Only NDC Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avicel RC-591 NF (MCC/Carboxymethylcellulose Sodium) NF Recalled by DuPont...
The Issue: Microbial Contamination of Non-Sterile Product: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fulvestrant Injection 250 mg/5 mL (50 mg/mL) For Intramuscular Use Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Naproxen Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorzoxazone Tablets USP 375 mg 100 Tablets Rx Only NDC Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by AVRIO...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...
The Issue: The firm is revising the Indication for Use, Contraindications, Warnings,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative...
The Issue: Labeled On-board instrument stability issue for current and future lots,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium ADVANTA VXT Vascular Graft Recalled by Atrium Medical Corporation Due...
The Issue: The product package may potentially contain a mismatched graft that does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnisound Gel Recalled by Accelerated Care Plus Corporation Due to...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog # BEK4511 Recalled by Bard Peripheral Vascular Inc Due to Due to...
The Issue: Due to misbranded products shipped to customers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog # BEK3411 Recalled by Bard Peripheral Vascular Inc Due to Due to...
The Issue: Due to misbranded products shipped to customers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.