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. 2,412 recalls have been distributed to Hawaii in the last 12 months.
Showing 19961–19980 of 27,645 recalls
Recalled Item: Liko Universal SlingBars Universal SlingBar" 350 Recalled by Hill-Rom, Inc....
The Issue: The center bolt of the sling bar, which connects the bar to the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol II Elecsys and cobas e analyzers 190 Recalled by Roche Diagnostics...
The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERO MHI-TM2000 Linear Accelerator System --- Common Name: Medical Linear...
The Issue: In rare cases the VERO/MHI-TM2000 Operator Console could set an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol III Recalled by Roche Diagnostics Operations, Inc. Due to Due to...
The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD ArcticGel Pads Product Usage: The Arctic Sun Temperature Management...
The Issue: Complaints were received of restricted/inaccurate flow rate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guardian II Hemostasis Valve Recalled by Vascular Solutions, Inc. Due to...
The Issue: Vascular Solutions became aware of a potential problem with the click...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spectra-System Dental Implant 2008 system is comprised of dental...
The Issue: Implant Direct Sybron Manufacturing, LLC is recalling GoDirect Implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity All Purpose Sponges Recalled by Covidien LLC Due to Compromised...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dynarex Specimen Containers Recalled by Dynarex Corporation Due to Exterior...
The Issue: Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hand-Held Scanner USB IT3800 For sample identification and tracking when...
The Issue: The hand-held barcode scanner model IT3800 used with the COBAS AmpliPrep...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity Gauze Sponges Recalled by Covidien LLC Due to Compromised sterility...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...
The Issue: Compromised sterility due to breach of barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.