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. 1,077 recalls have been distributed to Hawaii in the last 12 months.
Showing 8521–8540 of 47,764 recalls
Recalled Item: Phenylephrine HCl 20 mg added to 0.9% Sodium Chloride 250mL Bag Recalled by...
The Issue: Product Mix up; Product was compounded in 250 mL 5% Dextrose instead of 250...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UroPass Ureteral Access Sheaths Recalled by Olympus Corporation of the...
The Issue: Dilator tips may break in the package and in patients during surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviCare Patient Safety V3.9.200 to 3.9.600 Recalled by Baxter Healthcare...
The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voalte Patient Safety Recalled by Baxter Healthcare Corporation Due to...
The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW Endurance Extended Dwell Peripheral Catheter System Recalled by ARROW...
The Issue: Potential for catheter separation or leakage
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HMOD 70000-USA/QUADROX-iD Adult Recalled by Maquet Medical Systems USA Due...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HMO 71000-USA /QUADROX-i Adult Recalled by Maquet Medical Systems USA...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to Product packaging...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products NT-proBNP II Range Verifiers-For in vitro...
The Issue: May not meet the stability specifications for shelf life outlined in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Hardshell Cardiotomy Reservoir Recalled by Maquet Medical Systems USA...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Hardshell Cardiotomy Reservoir Recalled by Maquet Medical Systems USA...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Small Adult Recalled by Maquet Medical Systems USA Due to 1. An...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Pediatric Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to 1. An...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to 1. An accessory may...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.