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. 2,350 recalls have been distributed to Hawaii in the last 12 months.
Showing 35181–35200 of 47,764 recalls
Recalled Item: Baidyanath brand Sarivadi Bati Recalled by Butala Emporium, Inc. Due to The...
The Issue: The dietary supplements were found to contain lead, mercury and/or arsenic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baidyanath brand Arogyavardhini Bati Recalled by Butala Emporium, Inc. Due...
The Issue: The dietary supplements were found to contain lead, mercury and/or arsenic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baidyanath brand Rajahpravartini Bati Recalled by Butala Emporium, Inc. Due...
The Issue: The dietary supplements were found to contain lead, mercury and/or arsenic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baidyanath brand Gaisantak Bati Recalled by Butala Emporium, Inc. Due to The...
The Issue: The dietary supplements were found to contain lead, mercury and/or arsenic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baidyanath brand Shankh Bati Recalled by Butala Emporium, Inc. Due to The...
The Issue: The dietary supplements were found to contain lead, mercury and/or arsenic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baidyanath brand Brahmi Bati Recalled by Butala Emporium, Inc. Due to The...
The Issue: The dietary supplements were found to contain lead, mercury and/or arsenic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baidyanath brand Agnitundi Bati Recalled by Butala Emporium, Inc. Due to The...
The Issue: The dietary supplements were found to contain lead, mercury and/or arsenic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KAL Brand Amino Acid Complex Recalled by Nutraceutical International...
The Issue: Undeclared allergen, casein is a disclosed ingredient, but the word milk not...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD AffirM VPIII Microbial Identification Test Recalled by Becton Dickinson &...
The Issue: BD has confirmed that a portion of tests associated with the affected lots(...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX Multianalyte Controls Recalled by Alere San Diego, Inc....
The Issue: Alere San Diego is recalling the Alere Cholestech LDX Multianalyte Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Guide Wires for orthopedic procedures. Recalled by Zimmer, Inc. Due...
The Issue: Product labeling of these sterile guide wires (external carton label and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes...
The Issue: Manufacturer of 0.9% Sodium Chloride Flush Syringes recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD4 (SK3) Recalled by Becton, Dickinson and Company, BD Biosciences Due to...
The Issue: CD4 FITC label contains an error in the Spanish small text - it states CD8 FITC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascadian Farm Organic Cut Green Beans Recalled by General Mills, Inc Due to...
The Issue: General Mills is recall one lot of 10 ounce bags of frozen Cascadian Farm...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: syngo Lab Data Manager System - Product Usage: syngo Lab Recalled by Siemens...
The Issue: Software Issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThruPort Knot Pusher. This device is sold individually (Model KP1) Recalled...
The Issue: The configuration of the slot at the tip of the knot pusher may inhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Apotex Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1% Lidocaine HCl Injection Recalled by Hospira, Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: particulate matter identified as iron oxide,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ambitex NMD400 Nitrile Exam Gloves size medium. General Hospital and...
The Issue: Ambitex Nitrile NMD400 Exam Gloves size medium on exam hold were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to...
The Issue: Cross-threading of the hemostasis valve may occur if it is tightened with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.