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. 2,710 recalls have been distributed to Florida in the last 12 months.
Showing 30741–30760 of 55,837 recalls
Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroPort Orthopedics SCHANZ SCREW SELF DRILL Recalled by MicroPort...
The Issue: The item is being recalled due to an inadequate pouch seal. This defect has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torque wrench used on the bolts for the Symbia T2 model 10275008 Recalled by...
The Issue: The torque wrench used to tighten system bolts during installation was found...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for...
The Issue: Increased amount of residual blood present on the top of stopper well after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Death Wish Nitro Canned Cold Brew Coffee 11 oz Recalled by Death Wish Coffee...
The Issue: Potential for Clostridium Botulinum
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KIND Dark Chocolate Nuts and Sea Salt Bar-containing 12 /1.4 Recalled by...
The Issue: Outer box fails to declare the allergen walnuts, the individual bar is...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bio35 Recalled by Pro Bioteks Laboratories Due to Undeclared Soy
The Issue: Bio-35 has undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monarch Airway Clearance System Recalled by HILL-ROM MANUFACTURING, INC. Due...
The Issue: Monarch Electromagnetic Interference (EMI) may disrupt the operation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PapaZen 3300 capsule Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Intralipid 20% Recalled by Baxter Healthcare Corporation Due to Temperature...
The Issue: Temperature Abuse: A portion of this product lot was exposed to subfreezing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FIFTY SHADES 6000 capsule Recalled by Gadget Island, Inc Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: grande X 5800 capsule Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.