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. 2,375 recalls have been distributed to Hawaii in the last 12 months.
Showing 27281–27300 of 27,645 recalls
Recalled Item: i-STAT cTnI cartridges Product Usage: The i-STAT cTnl test is Recalled by...
The Issue: Abbott Point of Care has determined that i-Stat CTNL cartridges have the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4 Cervical (S4C) Revision Instruments (FW099R and FW101R). The S4C Recalled...
The Issue: Aesculap Implant Systems, LLC has initiated a voluntary removal of the S4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle Hip Solutions ALTRX Polyethylene Acetabular Liner Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of one lot of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Quasar Nuclear Medicine System Recalled by GE Healthcare, LLC...
The Issue: Accelerated fatigue of the lateral axis motion subsystem of the Infinia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium Heparin (LH) Recalled by Becton Dickinson...
The Issue: BD is conducting a recall of the BD Vacutainer Plus Plastic Plasma Separator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-STAT PT/INR cartridge Abbott Point of Care Inc. Abbott Park Recalled by...
The Issue: The i-STAT PT/INR cartridges have the potential to exhibit incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo.plaza. Radiological image processing system Recalled by...
The Issue: Siemens became aware of a potential malfunction when using syngo.plaza with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-01...
The Issue: Braemar has recently became aware of a battery related incident that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyroglobulin Antibody (TgAB) Calibrator - Product Usage: intended for IN...
The Issue: Some combinations of Calibrator lots and AlA PACKS resulted in Calibrator #6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TX1 Tissue Removal System Console. Model: TX1 TX1 Tissue Removal Recalled by...
The Issue: Two reasons for recall. 1. Incorrect pressure relief valve installed inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Columbus Tibia Plateau (component of the Columbus REVISION Knee System)...
The Issue: During an internal quality inspection, the tibia plateau was found to be out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Ultra-Short Magnetic Resonance Imaging System Recalled by Toshiba...
The Issue: The firm recalled due to a potentail problem with the position of the hold...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The brand name of the device is AlgiNot Recalled by Kerr Corporation Due to...
The Issue: The firm recalled the product because it may cure harder than expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enFlow IV Fluid Warmer (510k name: EFLOW IV FLUID WARMER Recalled by Vital...
The Issue: The EnFlow Warmer Strap does not meet the requirements of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOW-I Anesthesia System The system is intended for use in Recalled by...
The Issue: A technical alarm may be generated on the FLOW-i system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific Hitachi AST Reagent R1 : PE plastic bottle Recalled by...
The Issue: A Discrepancy was found on Hitachi AST (HA7 61) package insert. Limitations...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empi STIMC RE Self Adhesive electrodes. For use on TENS Recalled by Covidien...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...
The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.