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. 1,007 recalls have been distributed to Hawaii in the last 12 months.
Showing 17921–17940 of 47,764 recalls
Recalled Item: Hip Products Item Number: 1) 110010462 RingLoc Hip System Recalled by...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 154335 Oxford Partial Knee System Recalled by Biomet, Inc....
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Products: 141356 Regenerex Series-A Patella 3 Peg Recalled by Biomet,...
The Issue: Potential presence of elevated endotoxin levels that exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553)...
The Issue: This product has been confirmed to exhibit holes in the packaging, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta MONACO RTP Sytem Recalled by Elekta Inc Due to The Monaco RTP...
The Issue: The Monaco RTP Radiation Treatment Planning System may change the shape and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System - Product Usage: Intended for use Recalled by...
The Issue: There is potential for a white paper-type residue attached to the catheter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cefixime for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Subpotent Drug: low out of specification (OOS) test result observed in long...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KORE ORGANIC CBD Oil Watermelon 15mg* Recalled by Summitt Labs Due to...
The Issue: Chemical Contamination; product contains elevated levels of lead
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nizatidine Oral Solution Recalled by Amneal Pharmaceuticals of New York, LLC...
The Issue: CGMP Deviations: potential N-Nitrosodimethylamine (NDMA) amounts above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Recalled by B & B Pharmaceuticals, Inc. Due to Foreign Object...
The Issue: cGMP deviations: Presence of foreign material (Teflon)introduced at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Finasteride Plus 1.25 mg Capsule Recalled by MasterPharm LLC Due to Cross...
The Issue: Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD BBLTM Gram Crystal Violet 3.8L-- IVD Primary stain for Recalled by Becton...
The Issue: May exhibit increased levels of artifacts which could be difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBLTM Gram Crystal Violet 250mL-- IVD Primary stain for Recalled by...
The Issue: May exhibit increased levels of artifacts which could be difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBLTM Gram Stain Kit with Stabilized Iodine-- IVD For Recalled by Becton...
The Issue: May exhibit increased levels of artifacts which could be difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...
The Issue: The surgical gowns were manufactured in a facility that is not registered by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A2 C17/5 - Recalled by...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL Defibrillator/Monitor (Model number M4735A) - Product...
The Issue: The rotary therapy selector switch may fail, resulting in unexpected device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.