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. 1,889 recalls have been distributed to Hawaii in the last 12 months.
Showing 15441–15460 of 47,764 recalls
Recalled Item: FREESTYLE LIBRE 2 GLUCOSE MONITORING SYSTEM: Item number: 5658877 Recalled...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 42 cm (16.5 IN) APPX 2.6ml Recalled by ICU Medical, Inc. Due to Due to...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Closed Male Luer Recalled by ICU Medical, Inc. Due to Due to...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Closed Male Luer - Product Usage: Recalled by ICU Medical,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Controller - Product Usage: intended for use with a Recalled by Boston...
The Issue: May have been programmed with a less than optimal brightness setting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Appx 0.50 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 45" (114 cm) Appx 1.7 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 35" (89 cm) Appx 3.9 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Abre Venous Self-expanding Sent System Recalled by Medtronic Inc....
The Issue: Incorrect size printed on the device; packaging is labeled correctly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros¿ Closed Male Luer Recalled by ICU Medical, Inc. Due to Due...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDURITY Pulse Generator **** SN ********* St. Jude Medical Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Filtered Triple-Leg Extension Set - Intravascular administration set....
The Issue: BBMI has identified through complaints the potential for the extension set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diluent Recalled by Medline Industries Inc Due to Possible false negative or...
The Issue: Possible false negative or false positive results due to the product being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSURITY Pulse Generator **** SN ********* ST. JUDE MEDICAL Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuts.com brand Diced Dried Figs packaged in 1lb stand up gusset pouches....
The Issue: Undeclared almonds in diced fig product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Omeprazole Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZOMA-Jet 10 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...
The Issue: Defective Delivery System: customer complaints concerning the injector pen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZOMA-Jet 5 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...
The Issue: Defective Delivery System: customer complaints concerning the injector pen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.