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. 2,519 recalls have been distributed to Hawaii in the last 12 months.
Showing 11781–11800 of 27,645 recalls
Recalled Item: HeartStart MRx Processor Board PCA Replacement Kits 453563478461 Recalled by...
The Issue: Damaged ESD bags used for storing components in Processor PCA Replacement Kits
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 70 Recalled by Philips North America, LLC Due to When...
The Issue: When strain relief is lost at the stand side of the Stand MVS Trolley Cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 50 Recalled by Philips North America, LLC Due to When...
The Issue: When strain relief is lost at the stand side of the Stand MVS Trolley Cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Optilite Clinical Chemistry Analyzer. IVD. Model Number: IE700....
The Issue: A software issue that may affect the analyzer's result accuracy.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris PCEA Administration Set Recalled by BD SWITZERLAND SARL Due to The...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris PCEA Administration Set Recalled by BD SWITZERLAND SARL Due to The...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris PCEA Administration Set Recalled by BD SWITZERLAND SARL Due to The...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WRIGHT INBONE Tibial Tray Recalled by Wright Medical Technology Inc Due to...
The Issue: One lot of INBONE Tibial Trays is missing the plasma coating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: therascreen EGFR RGQ PCR Kit (24) Recalled by Qiagen Sciences LLC Due to...
The Issue: There is a risk for a false mutation positive result in rare cases resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAC Tray/5 Catheter Introducer Tray 8F Recalled by Argon Medical Devices,...
The Issue: Arterial Line Kits include thicker curved reverse-cutting needle with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Line Kit 20ga X 3" Recalled by Argon Medical Devices, Inc Due to...
The Issue: Arterial Line Kits include thicker curved reverse-cutting needle with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Line Kit 20ga X 3" Recalled by Argon Medical Devices, Inc Due to...
The Issue: Arterial Line Kits include thicker curved reverse-cutting needle with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerator a3600 Automation System using the Aliquoter Module (Inpeco P/N...
The Issue: In certain firmware versions, in case a Clot Detection error (error code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation System using the Aliquoter Module (Inpeco P/N FLX-212)...
The Issue: In certain firmware versions, in case a Clot Detection error (error code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab Augomation System using the Aliquoter Module (Inpeco P/N FLX-212)...
The Issue: Potential for discrepant patient results due to a potential for the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerator a3600 Automation System with Advia2120LAS Interface Module (P/N...
The Issue: The identified problem is an erroneous association between the carrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab Automation System with Advia2120LAS Interface Module (P/N FLX-219-00...
The Issue: The identified problem is an erroneous association between the carrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation System with Advia2120LAS Interface Module (P/N FLX-219-00...
The Issue: The identified problem is an erroneous association between the carrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oryx Cervical Screw Caddy Recalled by Innovasis, Inc Due to Cervical screw...
The Issue: Cervical screw caddies have incorrect text markings for the 4.5mm Fixed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.