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 7641–7660 of 47,764 recalls
Recalled Item: Robotics Pack Recalled by American Contract Systems, Inc. Due to During an...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Robotics Pack SAH Recalled by American Contract Systems, Inc. Due to During...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAVH Recalled by American Contract Systems, Inc. Due to During an internal...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Pack Recalled by American Contract Systems, Inc. Due to During an...
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Urology Wolson Pack Recalled by American Contract Systems, Inc....
The Issue: During an internal investigation, ACS identified that the components, I.V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solea Models 2.0 and 3.0 Laser Surgical Instrument Recalled by Convergent...
The Issue: It has been found that potential unintended laser activation can occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Male-Female Midsection with the following sizes and model numbers. a....
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethos Collar Stem Recalled by Onkos Surgical, Inc. Due to Potential for...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: The Guardian System Product Name: The Guardian Model/Catalog...
The Issue: Device reaching End of Service prematurely.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...
The Issue: Potential for breach of Tyvek seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroPICC 5Fr Dual Lumen Maximal Barrier Kit Recalled by Access Vascular,...
The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroPICC 5Fr Dual Lumen Recalled by Access Vascular, Inc Due to Specific...
The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EarlyVue VS30 Vitals Monitor Recalled by Philips North America Llc Due to A...
The Issue: A software issue prevents the monitor from alarming when the high/low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EarlyVue VS30 Vital Signs Monitor Recalled by Philips North America Llc Due...
The Issue: A software issue prevents the monitor from alarming when the high/low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...
The Issue: Patient beds are missing test values for electrical safety tests presenting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.