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. 1,132 recalls have been distributed to Florida in the last 12 months.
Showing 13341–13360 of 55,837 recalls
Recalled Item: Losartan Potassium & HCTZ Tablets 50mg/12.5 mg Recalled by Preferred...
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 Potassium & HCTZ Tablets 50mg/12.5 mg Recalled by Preferred...
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: Sirolimus Oral Solution Recalled by Apotex Corp. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Sirolimus Oral Solution recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Capsules Recalled by American Health Packaging Due to Failed...
The Issue: Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan HCTZ 100/12.5 mg Recalled by RemedyRepack Inc. Due to CGMP...
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 HCTZ 100/25 mg Recalled by RemedyRepack Inc. Due to CGMP...
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: MVASI (bevacizumab-awwb) Recalled by Amgen, Inc. Due to Defective container:...
The Issue: Defective container: loose crimp defect, potential loss of container integrity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.88-ounce green...
The Issue: Product(s) may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Keats London Vegan Hazelnut Dark Chocolate in a 4.93-ounce round Recalled by...
The Issue: Product(s) may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Keats London Vegan Irish Cream Truffles in a 4.93-ounce round Recalled by...
The Issue: Product(s) may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablet Recalled by SUN...
The Issue: Presence Of Foreign Substance: Customer complaint for the presence of dark,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-Release Tablet Recalled by SUN...
The Issue: Presence Of Foreign Substance: Customer complaint for the presence of dark,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: INTERGARD Woven Vascular Graft is a woven polyester graft coated Recalled by...
The Issue: Mislabeled: Product labeled as Intergard Woven Straight graft , D: 8 mm, L:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM CONTACT EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Cap-ONE Biteblock The cap-ONE Biteblock is intended Recalled by Nihon...
The Issue: Due to products being shipped/distributed to customers after the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xanax XR (alprazolam) extended-release tablets Recalled by Viatris Inc Due...
The Issue: Failed Dissolution Specifications: low out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: alprazolam XR extended-release tablets Recalled by Viatris Inc Due to Failed...
The Issue: Failed Dissolution Specifications: low out-of-specification dissolution test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ELITE PESEK ZMAN BIG BITE Net Wt. 1/94 oz (55g) Recalled by ELITE...
The Issue: Potential contamination with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.