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. 2,003 recalls have been distributed to Hawaii in the last 12 months.
Showing 5701–5720 of 47,764 recalls
Recalled Item: ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number:...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clarity and Clarity Diagnostics LLC Recalled by Wondfo USA Co Ltd Due to...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptococcal A rapid test kits Recalled by Wondfo USA Co Ltd Due to Wondfo...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE LUER LOCK DISPOSABLE SYRINGE WITHOUT NEEDLE Recalled by MEDLINE...
The Issue: It has been identified that testing documentation does not support that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptococcal A rapid test kits Recalled by Wondfo USA Co Ltd Due to Wondfo...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Independent Medical Co-op Inc. Recalled by Wondfo USA Co Ltd Due to Wondfo...
The Issue: Wondfo USA has identified unauthorized distribution of the Preview Strep A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE LUER SLIP DISPOSABLE SYRINGE WITHOUT NEEDLE Recalled by MEDLINE...
The Issue: It has been identified that testing documentation does not support that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tirzepatide 10 mg/0.5 mL Sterile Solution Recalled by Revive Rx LLC dba...
The Issue: Labeling: Label Mix-up - product labeled as tirzepatide contains...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUL-GLO Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GloStrips Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUL-GLO Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GloStrips Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amphotericin B Liposome for Injection Recalled by SUN PHARMACEUTICAL...
The Issue: Out of specification for assay
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Patient Information Center iX and Patient Information Center iX Expand...
The Issue: Event Catalog information does not save when copied and transferred from one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optum Nimbus II Plus Recalled by OptumHealth Care Solutions LLC Due to...
The Issue: Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sammy's Milk GOAT MILK TODDLER FORMULA Recalled by Graceleigh, Inc. dba...
The Issue: FDA inspection and investigation of firm's website and social media pages...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sammy's Milk GOAT MILK TODDLER FORMULA Recalled by Graceleigh, Inc. dba...
The Issue: FDA inspection and investigation of firm's website and social media pages...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG:...
The Issue: Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OES 4000 Hysteroscope Recalled by Olympus Corporation of the Americas Due to...
The Issue: The required leakage test was not performed following of a re-work for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Recalled by BD...
The Issue: Due to infusion set tubing drip chamber becoming detached from the tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.