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. 2,375 recalls have been distributed to Hawaii in the last 12 months.
Showing 25961–25980 of 47,764 recalls
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Dialysate Sack: 1) UDI-M535SAK3010 Recalled by NxStage Medical, Inc....
The Issue: May contain endotoxin levels which have been confirmed to exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips QCPR Meter - used with MRx Product Usage: The Recalled by Philips...
The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound System Product Usage: The SC2000 ultrasound imaging...
The Issue: The application may underestimate the EROA (Effective Regurgitant Orifice...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ray Station 4.9 Ray Station 5 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: Software issue with Center Beam in Field functionality. Issue can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel Recalled...
The Issue: The mounts on the monitor may have an insufficient (missing or incomplete) weld.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Limbrel (flavocoxid 500 mg) capsules Recalled by Primus Pharmaceuticals,...
The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Limbrel500 (flavocoxid and citrated zinc bisglycinate) 500 mg/50 mg capsules...
The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Limbrel250 (flavocoxid and citrated zinc bisglycinate) 250 mg/50 mg capsules...
The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Limbrel (flavocoxid 250 mg) capsules Recalled by Primus Pharmaceuticals,...
The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biograph Horizon - PET/CT Recalled by Siemens Medical Solutions USA, Inc....
The Issue: Error introduced into PET images acquired and reconstructed with VJ20A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux VITEK 2 Gram Positive Cefoxitin Screen Recalled by bioMerieux,...
The Issue: Customer reports indicated an increase in the rate of non-detected MRSA in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Product Usage: Usage: Centricity PACS-IW with...
The Issue: Potential that one or more image series may be missing from an exam without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity...
The Issue: Potential that one or more image series may be missing from an exam without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets...
The Issue: CGMP deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: O-arm 1000 mobile image-intensified fluoroscopic x-ray system Recalled by...
The Issue: Software update ("SW Update 3.2.1") is being implemented to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Select Cycler (SW v.2.8.7) Recalled by Fresenius Medical Care Renal...
The Issue: The recalling firm identified a software issue related to the Patient Line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cefuroxime Recalled by JCB Laboratories LLC Due to Subpotent Drug: The...
The Issue: Subpotent Drug: The product is sub-potent prior to its 90-day beyond use date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panera Chive&Onion Reduced Fat Cream Cheese Spread Recalled by Panera, LLC...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ready-to-Eat Powdered Peanut Butter in 1 lb (16 oz.) plastic jars Recalled...
The Issue: Analytical results for generic non-pathogenic E. coli surpassed firm's...
Recommended Action: Do not consume. Return to store for a refund or discard.