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. 2,338 recalls have been distributed to Hawaii in the last 12 months.
Showing 39121–39140 of 47,764 recalls
Recalled Item: Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Saba Shark Cartilage Complex Dietary Supplement Recalled by AMS Health...
The Issue: The product is being recalled due to the potential presence of Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AMS Monarc + Subfascial Hammock with Tensioning Suture Recalled by American...
The Issue: During routine periodic packaging testing, AMS identified that in simulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdVance"Male Sling System Recalled by American Medical Systems, Inc. Due to...
The Issue: During routine periodic packaging testing, AMS identified that in simulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Intuition Distal Femoral Jig Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: Issuing a device correction because if the pin bushing is over loaded or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5% Dextrose and 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Water for Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactated Ringer's Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactated Ringer's and 5% Dextrose Injection Recalled by Hospira Inc. Due to...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Normosol-R Multiple Electrolytes Injection Type 1 Recalled by Hospira Inc....
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Normosol-R pH 7.4 Multiple Electrolytes Injection Type 1 Recalled by Hospira...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hapi Pudding Recalled by J F C International Inc Due to Product's label...
The Issue: Product's label fails to declare milk.
Recommended Action: Do not consume. Return to store for a refund or discard.