Product Recalls in Florida
Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,866 recalls have been distributed to Florida in the last 12 months.
Showing 13221–13240 of 55,837 recalls
Recalled Item: Pertussinum Recalled by Washington Homeopathic Products, Inc. Due to cGMP...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candida Albicans Recalled by Washington Homeopathic Products, Inc. Due to...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Influenzinum Recalled by Washington Homeopathic Products, Inc. Due to cGMP...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candida Parapsilosis Recalled by Washington Homeopathic Products, Inc. Due...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tivicay (dolutegravir) Tablets 50 mg Recalled by GlaxoSmithKline LLC Due to...
The Issue: Labeling: incorrect or missing lot and/or expiration date. An incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zonisamide Capsules USP Recalled by Direct Rx Due to CGMP Deviations: Gaps...
The Issue: CGMP Deviations: Gaps in the quality system in the Quality Control...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one...
The Issue: The outer package is mislabeled and the package contains a different IOL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA Autosuture Circular Stapler with DST Series Technology Recalled by...
The Issue: The affected staplers have the potential for the staple guide to not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...
The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...
The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip Recalled by NeuMoDx...
The Issue: There is a potential for reduced analytical sensitivity for samples in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anagrelide Capsules USP Recalled by Teva Pharmaceuticals USA Inc Due to...
The Issue: Failed Dissolution Specifications- Low Out-Of-Specification results obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Pot/HCTZ 100/12.5 mg 90 Tabs NDC 72189-290-90 Packaged and Recalled...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits .
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Pot/HCTZ 50/12.5 mg 90 Tabs NDC 72189-297-90 Packaged and Recalled...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits .
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Pot/HCTZ 100/25 mg 90 Tabs NDC 72189-289-90 Packaged and Recalled...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits .
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wise Woman Herbals Standardized Kava Glycerite Recalled by EarthLab Inc Due...
The Issue: The microbial test result is found to be out of specification due to high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wise Woman Herbals Sleepytime Glycerite. Product is liquid and strength...
The Issue: The microbial test result is found to be out of specification due to high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wise Woman Herbals Kava Capsules Recalled by EarthLab Inc Due to The...
The Issue: The microbial test result is found to be out of specification due to high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PLANET OAT Chocolate Chip Cookie Dough Recalled by HP Hood LLC Due to...
The Issue: Product may contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medline Pill Splitters Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Product lid (which houses a blade) is coming unhinged from the base, thus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.