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. 2,582 recalls have been distributed to Hawaii in the last 12 months.
Showing 2501–2520 of 47,764 recalls
Recalled Item: ELECTRO BUZZ Recalled by SAINI TRADE INC Due to Undeclared Chloropretadalafil
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTRA ARMOR Recalled by SAINI TRADE INC Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Male Ultra Pro Recalled by SAINI TRADE INC Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MALEXTRA Recalled by SAINI TRADE INC Due to Undeclared Propoxyphenylsildenafil
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Male Ultra Recalled by SAINI TRADE INC Due to Undeclared Propoxyphenylsildenafil
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Breckenridge...
The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Breckenridge...
The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug Group LLC...
The Issue: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " Recalled by Prismatik...
The Issue: Due to packaging mix up. Package of finished devices were reported to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges...
The Issue: Product was incorrectly assigned GEN 88 instead of GEN 83 on product carton,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plus Initial Drill Recalled by Straumann USA LLC Due to The batch was...
The Issue: The batch was produced without the laser engraving of 7 mm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Augmedics Perc Pin Adaptor Recalled by Augmedics Ltd. Due to The perc pin...
The Issue: The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Recalled by Medical...
The Issue: Potential for DC Power Supply housing to become hot to the touch and deform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pruitt Occlusion Catheter. Catalog Numbers: 2103-36 Recalled by LeMaitre...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X)...
The Issue: Potential for the presence of visible foreign matter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09 Recalled by...
The Issue: During internal product testing, it was observed that some packages to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Craniotomy Kit Recalled by Integra LifeSciences Corp. (NeuroSciences)...
The Issue: Inadequate weld that can potentially cause the product to disassemble.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN Disposable Perforator Recalled by Integra LifeSciences Corp....
The Issue: Inadequate weld that can potentially cause the product to disassemble.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.