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 55661–55680 of 55,837 recalls
Recalled Item: ULTRA Fabric Reinforced Surgical Gown Recalled by Kimberly-Clark Corporation...
The Issue: The impacted product was not intended for commercial distribution to end users.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M3150 Information Center Local Database Recalled by Philips Electronics...
The Issue: Potential for early component failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Standard Polyaxial Screw Assembly 6.5MM x 55MM. Part # Recalled by...
The Issue: The recall was initiated because Alphatec Spine confirmed that the TI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BCS(R) Behring Coagulation System Recalled by Siemens Healthcare...
The Issue: Firm has confirmed that if the Cleaner SCS vial becomes empty after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Pointe Scientific CK-MB Isoenzyme Control Pointe Scientific CK-MB Level...
The Issue: Incorrect control range in product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morphine Sulfate Extended Release tablet Recalled by Physicians Total Care,...
The Issue: Labeling: Label mix-up; Bottles labeled to contain Morphine Sulfate IR may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Immediate Release tablet Recalled by Physicians Total Care,...
The Issue: Labeling: Label mix-up; Bottles labeled to contain Morphine Sulfate IR may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Canon Solid State X-ray Imager (Flat Panel/Digital Imager) Recalled by Canon...
The Issue: Screws holding the 55REF circuit board are loosening and roaming inside of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 0-arm Imaging System with Software Version 3.1.1 Recalled by...
The Issue: Software Version 3.1.1 does not meet navigational accuracy.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789504001 VerSys Femoral Head Provisional 40mm -3.5 00789504002 VerSys...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780302201 MIS 12/14 Slotted Femoral Head Provisional -2X22 00780302202 MIS...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: . 00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780302801 MIS 12/14 Slotted Femoral Head Provisional -3.5X28 00780302802...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00789503201 VerSys Femoral Head Provisional 32mm -3.5 00789503202 VerSys...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 100789502202 VerSys Femoral Head Provisional 22mm +0 00789502203...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.