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 25741–25760 of 30,686 recalls
Recalled Item: ***Baxter***BURETROL Solution Set***105" (2.7 m) 150 mL Burette***Drip...
The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patella 38mm Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ascenda Intrathecal Catheter models 8780 and 8781 Recalled by...
The Issue: Medtronic is removing specific lots of the Ascenda Intrathecal Catheters and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibila Insert UC Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Post-Op Surgical Kits . Kit includes: Amerigel Wound Dressing...
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management....
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS Tibial Insert Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Serrated Soft Tissue Shields. Orthopedic surgical instruments Recalled by X...
The Issue: Revision B of the tissue shields of the device was 7 mm longer than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Daily Dressing Advanced 3-in-1 Hydrogel Recalled by Amerx Health...
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Hydrogel Saturated Gauze Dressing Recalled by Amerx Health Care...
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibila Insert CK Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowCOUPLER. An implantable device that is used to detect blood Recalled by...
The Issue: Baxter Healthcare is recalling the FlowCOUPLER Device because there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pivot Bipolar Cup 22x42/43-51/53mm Recalled by Ortho Development Corporation...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table with Dual 2 Way Drop Section...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Foley Urinary Catheter Insertion Tray with 10cc syringe Recalled by...
The Issue: Labeling error: The manufacturing date is the same as the expiration date....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The Recalled...
The Issue: An on-site evaluation of the equipment parts that attach the Beta Assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...
The Issue: The temperature probe does not properly connect to the temperature port.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.