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. 2,322 recalls have been distributed to Hawaii in the last 12 months.
Showing 40681–40700 of 47,764 recalls
Recalled Item: Circular Lock Screws Recalled by Genesys Orthopedics Systems, LLC Due to The...
The Issue: The recall is being initiated because MK Precision (the Circular Lock Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: A glass defect was found on the interior...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ah! Laska Organic Cocoa Non Dairy Chocolate Mix Recalled by Koru Pacific...
The Issue: Internal testing confirmed the presence of milk allergen in finished product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Just Great Stuff Chocolate Dream Greens Recalled by Betty Lou's, Inc. Due to...
The Issue: Undeclared milk which was a contaminant of the dark chocolate ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: triple therapy Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: This recall is due to out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydrOXYzine Hydrochloride Oral Solution Recalled by Hi-Tech Pharmacal Co.,...
The Issue: Failed Impurity/Degradation Specification; out-of-specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Wockhardt Usa Inc....
The Issue: Failed Dissolution Specifications: failure of dissolution test observed at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glytone Acne Recalled by Genesis Pharmaceutical, Inc. Due to Failed...
The Issue: Failed Stability Specifications: Out of specification results for viscosity...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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: 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: 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: Philips Medical Systems Computed Tomography X-ray systems (Brilliance CT...
The Issue: A customer reported that the table top had become free floating. A Field...
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: 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: Xzen 1200 Recalled by Nova Products, Inc. Due to Undeclared Amounts
The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XZEN PLATINUM Recalled by Nova Products, Inc. Due to Undeclared Amounts
The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.