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. 967 recalls have been distributed to Hawaii in the last 12 months.
Showing 32041–32060 of 47,764 recalls
Recalled Item: Lodrane D (Brompheniramine maleate 4 mg and Pseudoephedrine HCl 60 mg)...
The Issue: Labeling: Not Elsewhere Classified: correctly labeled bottles were packaged...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Radiesse (+) Lidocaine Recalled by Merz North America, Inc. Due to...
The Issue: Complaints reported of Radiesse (+) unable to be expelled from the syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-wire Recalled by Integra LifeSciences Corp. Due to The affected K-wires do...
The Issue: The affected K-wires do not meet specification requirements. Specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Kalare DREX-KL80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6534-08N InterActive¿ Implant Open-Tray Transfer Narrow Part Number:...
The Issue: The incorrect sized product, InterActive Implant Open-Tray Transfer Wide,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Ultimax DREX-ULT80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxycodone HCl Recalled by West-Ward Columbus Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specification; 9 month stability
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Recalled by Galderma Laboratories, L.P. Due to Labeling:...
The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: Some expiries and lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Divalproex Sodium Delayed-release Tablets USP Recalled by Teva North America...
The Issue: Failed Tablet/Capsule Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed a potential for biased calcium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Product Usage: The Monaco system is used Recalled by...
The Issue: When DICOM exporting a 3D Monaco plan and the "Composite Field Sequencing"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas¿ Liat Influenza A/B Quality Control Kit Recalled by Roche Molecular...
The Issue: Kit labeled with the incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dome Centric component ( 01.04227.005) from the Anatomical Shoulder (AS)...
The Issue: In some cases it has been difficult or not possible to disassemble the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Comprehensive ventilator Recalled by Carefusion 211 Inc dba Carefusion...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Standard ventilator- Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Comprehensive ventilator- Recalled by Carefusion 211 Inc dba Carefusion...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVEA Standard with Compressor ventilator- Recalled by Carefusion 211 Inc dba...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.