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. 2,391 recalls have been distributed to Hawaii in the last 12 months.
Showing 22701–22720 of 47,764 recalls
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne CDx Test Results Recalled by Foundation Medicine, Inc. Due to...
The Issue: An incorrect test result for a single analyte may have been reported for up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protexis Neoprene Surgical Glove Recalled by Cardinal Health 200, LLC Due to...
The Issue: Labeling issue in that the breakthrough (i.e., permeation) times for two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by Akorn, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...
The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GSMS Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due to CGMP...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...
The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminister Irbesartan Tablets Recalled by Sciegen Pharmaceuticals Inc Due...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminster Irbesartan Tablets Recalled by Westminster Pharmaceuticals Llc...
The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Feast Mode Flavors Garlic Beer Seasoning Recalled by Feast Mode Blending &...
The Issue: Feast Mode Garlic Beer Seasoning is mislabeled as "Gluten Free"
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Levetiracetam in 0.54 % Sodium Chloride Injection 1 Recalled by Dr. Reddy's...
The Issue: Labeling: Label Error on Declared Strength; the pre-printed text on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Apple juice concentrate and organic apple juice concentrate in 52 gallon...
The Issue: The apple juice concentrates contain high levels of inorganic arsenic. The...
Recommended Action: Do not consume. Return to store for a refund or discard.