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 25821–25840 of 30,686 recalls
Recalled Item: Zimmer Dental Tapered Screw-Vent Implant Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Dental is conducting a voluntary recall of a single lot of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a...
The Issue: A potential splitting of the surface treatment of the thread ends on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter...
The Issue: Potential for inadvertent scalpel stick injury involving the safety scalpel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonopet Ultrasonic Surgical System Console Recalled by Stryker Instruments...
The Issue: The firm received complaints regarding insufficient irrigation to the tip of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MK5 NX Controller--Wheelchair controller Recalled by Invacare Corporation...
The Issue: M41 Powered Wheelchairs received through Invacare Service Parts (ISP) have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...
The Issue: Complaints of failed calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis EMPIRA RX PTCA Dilatation Catheter Recalled by Cordis Corporation Due...
The Issue: The balloon may exhibit resistance to the removal of the balloon cover....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis EMPIRA NC RX PTCA Dilatation Catheter Recalled by Cordis Corporation...
The Issue: The balloon may exhibit resistance to the removal of the balloon cover....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...
The Issue: Complaints of failed calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT: product code 882482 Recalled by Philips Medical Systems...
The Issue: Flat Panel Display (FPD) failed to remain securely locked in the deployed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable StrykeFlow Tip Recalled by Stryker Endoscopy Due to Internal...
The Issue: Internal review found that six lots of Disposable StrykeFlow Tips were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LP Recalled by Laser Peripherals LLC Due to Mislabeling
The Issue: Laser Peripherals LLC is recalling DBLF-60-2 Bare Laser due to a mislabeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Name: Pasteur Pipets Recalled by ORIGIO, Inc Due to Identification of...
The Issue: Identification of packaging breach of the nylon pouch sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific ENDOTAK RELIANCE¿ SG Recalled by Boston Scientific CRM...
The Issue: A review of manufacturing test records for Boston Scientific ENDOTAK...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 mL Reaction Vessels (a consumable of the Abbott m2000sp Recalled by Abbott...
The Issue: Abbott Molecular identified that some of the 5 ml Reaction Vessels (RVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo¿ Advanced Perfusion System 1 100/120V AC Recalled by Terumo...
The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap with Povidone-Iodine Solution Recalled by Baxter Healthcare...
The Issue: Inadequate iodine and packaging related defects.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo¿ Advanced Perfusion System 1 220/240V AC Recalled by Terumo...
The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Series High Energy Linear Accelerator - Models: Novalis Tx Recalled by...
The Issue: Trend in reports of unexpected decrease in beam output in C-series High...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion Set because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.