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. 2,615 recalls have been distributed to Florida in the last 12 months.
Showing 50521–50540 of 55,837 recalls
Recalled Item: Terazosin Hydrochloride Capsules Recalled by Teva Pharmaceuticals USA, Inc....
The Issue: Labeling -label error on declared strength: unopened, sealed bottle of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stereotactic Circular Collimator - 3D Line stereotatic Hardware Accessories...
The Issue: Potential for clinical errors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRI Cocaine Metabolite Assay Recalled by Microgenics Corp Due to...
The Issue: Surveillance of reagent stability for specific lots of DRI Cocaine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Super-DMZ Rx 2.0 Capsules Recalled by Mira Health Products Ltd. Due to...
The Issue: Marketed without an Approved NDA/ANDA; product contains the steroid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: B-50 capsules Recalled by Mira Health Products Ltd. Due to Marketed without...
The Issue: Marketed without an Approved NDA/ANDA; product found to contain methasterone...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: METHA-DROL Extreme capsules Recalled by Mira Health Products Ltd. Due to...
The Issue: Marketed without an Approved NDA/ANDA; product found to contain dimethazine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Torrent Pharma Inc Due to Defective...
The Issue: Defective Container; This action is being taken as a precautionary measure...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: New Sun Immune 101 Recalled by New Sun Inc Due to Potential E. coli...
The Issue: Positive E.coli
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: New Sun JLB Combination Recalled by New Sun Inc Due to Potential E. coli...
The Issue: Positive E.coli
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tapered Navigator Certain Surgical Kit Product Usage: Molded plastic tray...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator Surgical Kit Product Usage: Molded plastic tray used in Recalled...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit Product Usage: Molded plastic tray used...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit For Certain Internal Connection Product...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contra-Angle Torque Driver Kit For Certain and External Connection Product...
The Issue: During recent revised sterilization validation testing, the included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.7mm and 5.0mm Dynamic Locking Screw (DLS) Product Usage: 3.7mm Recalled by...
The Issue: All lots of 3.7mm and 5.0mm Dynamic Locking Screw (DLS) were recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX 16-Slice CT Scanner System. Used as a whole-body computed Recalled by...
The Issue: A pinch point at the end of the table top can cause injury.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense...
The Issue: The firm issued a clinical alert after users reported an issue where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esbelder Siloutte Suplemento Alimenticio Recalled by Herbal Give Care Llc...
The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esbelin Siloutte Mezcal Herbal con L-Carnitine Suplemento Alimenticio...
The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Esbelin Siloutte Te Recalled by Herbal Give Care Llc Due to Undeclared...
The Issue: Marketed Without an Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.