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 6761–6780 of 27,645 recalls
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to a failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Hoffmann LRF Recalled by Stryker GmbH Due to Stryker has identified...
The Issue: Stryker has identified a nonconformance in specific lots of Hoffmann LRF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial mobile application Recalled by Securitas Healthcare LLC Due to The...
The Issue: The mobile application for Android devices downloaded from the Google Play...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA comprises AST Filters in conjunction with VITEK MS Recalled by...
The Issue: For users with MYLA V4.8.X / V4.9 that use VITEK MS to identify organisms as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avanos Ballard Oral Care Swab Recalled by Avanos Medical, Inc. Due to...
The Issue: Incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE designed specifically for clinical use in the Recalled by...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE PRO-Analyzer designed specifically for clinical use in the...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE- Analyzer designed specifically for clinical use in the Recalled...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE PRO )-Analyzer designed specifically for clinical use in Recalled...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD* ACCESS Closed Suction System for Neonates/Pediatrics Recalled by...
The Issue: Potential for product manifold to crack during use on patients, possibly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD ACCESS Closed Suction System for Neonates/Pediatrics Recalled by...
The Issue: Potential for product manifold to crack during use on patients, possibly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEAR Implant (Bridge-Enhanced ACL Restoration) Recalled by Miach...
The Issue: The field action was initiated in February of 2023 and was limited to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno systems with a Siemens Healthineers table or Trumpf/MAQUET...
The Issue: If, during the procedure, X-ray has been released and a image has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EndoHPB Bipolar Radiofrequency (RF) Catheter 8F (2.7mm). A...
The Issue: Cease use of the Habib EndoHPB Bipolar RF Catheter with the ERBE VIO3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno systems with a Siemens Healthineers table or a Recalled by...
The Issue: In the event of any unintended table movement, the system may not detect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATITUDE NXT Remote Patient Management System Recalled by Boston Scientific...
The Issue: Under specific circumstances, the U.S. product registration system did not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOLOC 3DSi CLAW II 4 HOLE Plate Recalled by Wright Medical Technology,...
The Issue: Stryker has identified an issue that impacts two specific lots of CLAW" II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOLOC 3DSi CLAW II 4 HOLE Plate Recalled by Wright Medical Technology,...
The Issue: Stryker has identified an issue that impacts two specific lots of CLAW" II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Insulin Syringe 0.5mL Recalled by Becton Dickinson & Company...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml Recalled by...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.