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 24961–24980 of 47,764 recalls
Recalled Item: SDA Senna Syrup (Sennosides 8.8mg) Recalled by RIJ Pharmaceutical LLC Due to...
The Issue: CGMP Deviations: Products are being recalled due to an out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gericare Diocto Liquid (Docusate Sodium 50mg) Recalled by RIJ Pharmaceutical...
The Issue: CGMP Deviations: Products are being recalled due to an out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: The recalling firm has identified two lots of test strips that are out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Inform II Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: The recalling firm has identified two lots of test strips that are out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Aviva Plus Test Strip Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: The recalling firm identified four US lots of test strips out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Sodium Slides Recalled by Ortho-Clinical Diagnostics Due to Potential...
The Issue: Potential for positively biased results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drainer(R) Centesis Catheters: (a) Recalled by Vascular Solutions, Inc. Due...
The Issue: The supplier of Drainer(R) centesis catheters notified Vascular Solutions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Torque Limiting Handle Recalled by Synthes (USA) Products LLC Due to...
The Issue: The adapter may demonstrate a degradation of function as the final products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: remel SUPERPACK CS/ 500 SEG/FLASK Recalled by Thermo Fisher Due to Product...
The Issue: Product may fail performance testing for S aureus ATCC 43300.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) 0.1 mg/day Recalled by Noven...
The Issue: Defective Delivery System: no longer meets the specification for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) 0.0375 mg/day Recalled by Noven...
The Issue: Defective Delivery System: no longer meets the specification for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...
The Issue: The devices may have been assembled with an internal component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...
The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P.R.O. Matt: (a) PROMATT PLUS 36 X 76 MATRESS Recalled by Joerns Healthcare...
The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...
The Issue: The devices may have been assembled with an internal component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...
The Issue: Ingress of fluids into the device can affect various electronic circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware Medtronic HVAD System for cardiac use. Including the following...
The Issue: Possible transient electrical connection interruption between an HVAD System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagNA Pure 24 System Recalled by Roche Molecular Systems, Inc. Due to...
The Issue: Cross-contamination of samples has been reported when running the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew ANTHOLOGY POROUS HIGH OFFSET STEM Recalled by Smith & Nephew,...
The Issue: Three lots of Anthology HO Porous size 7 stems were manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis Recalled by...
The Issue: The bottles are mislabeled with an incorrect part number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.