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. 2,386 recalls have been distributed to Hawaii in the last 12 months.
Showing 23881–23900 of 27,645 recalls
Recalled Item: Pipeline Embolization Device (PED). Used endovascular treatment of adults...
The Issue: Potential for the PTFE (polytetrafluoroethylene) coating to delaminate and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS-C Femoral Nonporous Rt Sz 6 Recalled by Ortho Development Corporation Due...
The Issue: A femoral component containing pegs was found in a box for the pegless version.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Linear Accelerator (LINAC) models. Product Usage: deliver X-ray...
The Issue: Siemens Radiation Oncology became aware that customers may be using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRABECULAR METAL MODULAR ACETABULAR SYSTEM Recalled by Zimmer, Inc. Due to...
The Issue: The shell was missing the locking ring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 550 TxT Treatment Table of the Digital Linear Accelerator (LINAC) Recalled...
The Issue: Table may lose calibration during patient treatment, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alligator Retrieval Device (ARD). Used in the peripheral and...
The Issue: Potential for the PTFE (polytetrafluoroethylene) coating to delaminate and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ-IO 45mm (40kg & up) Needle Set Recalled by Vidacare Corporation Due to...
The Issue: The voluntary recall is due to the needle set not meeting its specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Recalled by...
The Issue: Urgent Device Correction notifications are being sent to USA distributors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henora 300psi I.V. Catheter Extension Set Product Usage: Recalled by RGI...
The Issue: Problem with low adhesion of the tubing to luer connection which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E9 Ultrasound System Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sit/stand Rolling Walker Recalled by Central Purchasing LLC DBA Harbor...
The Issue: Harbor Freight Tools intiaited a recall of Sit/Stand Rolling Walker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 Proton Therapy System for cancer treatment. Recalled by Ion Beam...
The Issue: While the Proteus 235 is in the pencil beam scanning (PBS) treatment mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Block assembly-lock stop subframe of service latch was not manufactured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INOmax DSIR Recalled by INO Therapeutics (dba Ikaria) Due to An anomaly...
The Issue: An anomaly impacts the monitoring system of INOmax DSIR Plus (software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Osteo-Clage System consists of stainless steel cable/sleeves and...
The Issue: Manufacturing of these devices with a grade of stainless steel that is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker PenAdapt" Recalled by Stryker Instruments Div. of Stryker...
The Issue: During packaging verification testing, a failure occurred due to cuts in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ToxCup Drug Screen Cup Recalled by Branan Medical Corporation Due to May be...
The Issue: May be labeled with incorrect result interpretation graphics on the ToxCup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products FS Diluent Pack 3 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed the potential for lower than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Acumed Tension Band Pin is a fixation pin which Recalled by Acumed LLC...
The Issue: Certain lots of Acumed Tension Band Pins are being recalled because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Specialty Diluent Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed the potential for lower than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.