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. 2,512 recalls have been distributed to Hawaii in the last 12 months.
Showing 12861–12880 of 27,645 recalls
Recalled Item: Transducer S8-3t UDI (01)00884838073524 Can be used as Recalled by Philips...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S7-3t UDI (01)00884838061439 Can be used with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S8-3t UDI (01)00884838067523 Can be used with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transducer S7-3t UDI (01)00884838067530 Used as accessory with: Recalled by...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPROTTE Lumbar with Introducer Recalled by Pajunk GmbH Due to Problem with...
The Issue: Problem with packaging sealing process which affects sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ApexPro Telemetry Server System. Also identified as Modification To: ApexPro...
The Issue: May not provide visual and/or audible alarms at the CARESCAPE Central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dario Blood Glucose Monitoring System Recalled by LABSTYLE INNOVATIONS Due...
The Issue: The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.3 CM BELL-single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 701 and 702 Analyzer/Module-RF interference claims for the Recalled...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 311 Recalled by Roche Diagnostics Operations, Inc. Due to Tina-quant...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomograpy and Computed Tomography System Recalled by...
The Issue: Potential sporadic software bugs in R001.3.0.0.750505 software version may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pharos Excimer Laser Recalled by Ra Medical Systems, Inc. Due to At doses of...
The Issue: At doses of less than 100 mJ, in custom and auto repeat modes, a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The...
The Issue: Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CentriMag Acute Circulatory Support System Motor Recalled by Thoratec...
The Issue: Reports have been received of the CentriMag Systems experiencing motor and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMP RVRS Shoulder Baseplates Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMOD PORCOAT HA GLENTRAY Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALL NOSE GUIDE WIRE 80CM Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Hip systems Recalled by Zimmer Biomet, Inc. Due to Elevated levels...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HA Pins (DFS HA Cort Screw) Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.