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. 937 recalls have been distributed to Hawaii in the last 12 months.
Showing 40861–40880 of 47,764 recalls
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck¿ Recalled by Teleflex Medical Due to Complaints were received...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Standard Length...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck Vista Optical Bladeless Laparoscopic Access Port Recalled by...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mm Weck Vista Cannula-only Recalled by Teleflex Medical Due to Complaints...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal (ISP) Recalled by Philips Medical Systems (Cleveland)...
The Issue: During SPECT reconstructions using Attenuation Correction and Scatter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 mm x 100mm Weck Vista Universal Cone Open Access Recalled by...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Vista Universal Laparoscopic Port Recalled by Teleflex Medical Due to...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck Vista Universal Cannula Recalled by Teleflex Medical Due to...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck¿ Vista" Universal Laparoscopic Port Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck Vista Universal Balloon Open Access Port - Standard Length (70mm)...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12MM X 100MM Weck¿ Vista" UNIVERSAL CONE OPEN ACCESS Recalled by...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12mm Weck¿ Vista" Cannula-only Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Long Length...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 mm Weck¿ Vista" Optical Bladeless Laparoscopic Access Port Recalled...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perrigo Recalled by Paddock Laboratories, LLC Due to Presence of Particulate...
The Issue: Presence of Particulate Matter Perrigo is recalling seven lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...
The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.