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. 2,549 recalls have been distributed to Hawaii in the last 12 months.
Showing 6521–6540 of 47,764 recalls
Recalled Item: Kroger Cherry Cough Drops Recalled by Bestco LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Equate Cherry Cough Drops Recalled by Bestco LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Family Wellness Cherry Cough Drops Menthol cough suppressant/Oral Anesthetic...
The Issue: CGMP Deviations: Potential Glass and Silicone particulates in product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeza Skin Protectant Recalled by OMEZA LLC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeza Lidocaine Lavage pain relief oil 10*2mL VIALS Recalled by OMEZA LLC...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TrueDent Clear Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent Yellow Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent Cyan Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent Magenta Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent White Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS5HND / Integra Cranial access kit (without Prep Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : HITHSP04 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7260 / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7270 / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7250 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : 31156 / COMBO KIT CONTAINS INS-8301 Recalled by Integra LifeSciences Corp....
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INS7280 / Integra¿ Cranial Access Kit. For access to the Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITHND / Integra¿ Cranial access kit (without Prep Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : HITHSP06 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITH / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.