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. 2,616 recalls have been distributed to Florida in the last 12 months.
Showing 45861–45880 of 55,837 recalls
Recalled Item: siemens Dimension¿ Phenytoin Flex¿ Reagent Cartridge The PTN method used...
The Issue: Internal testing has confirmed a low absorbance range between the levels 1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed...
The Issue: The Easy-Care Care-Lock feature installed at the foot of the bed may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety...
The Issue: An investigation identified that the product was incorrectly manufactured as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare Perfecto 2 V Oxygen Concentrator The finished device is Recalled by...
The Issue: It was determined that a defective sieve bed subassembly enabled zeolite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego systems Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A cable inside the C-arm systems may have been routed in an inappropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Mobile X-ray Systems used to take diagnostic radiographic exposures...
The Issue: There is a potential for unintended and erratic motion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoswift PGCL [poly(glycolide-co-caprolactone)] Absorbable Surgical Suture...
The Issue: CP Medical Inc. is recalling five lots of Monoswift PGCL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Nature's Place Organic Campfire Trail Mix Recalled by United Natural...
The Issue: The various trail mixes may contain undeclared cashew kernels.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mars Chocolate North America Milk Chocolate M & M's Net Recalled by Mars...
The Issue: Mars Chocolate North America is recalling M & Ms due to undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Straumann Bone Level Tapered Implant 04.1 mm RC Recalled by Straumann USA,...
The Issue: Assembled with Narrow Connect (NC) transfer piece instead of Regular Connect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE /IMMULITE 1000 Systems COR Cortisol Recalled by Siemens Healthcare...
The Issue: Customer complaints were received for positive bias reported on the controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status+ The Clinitek...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status Connect System...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status Power Supply...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module Recalled by GE Healthcare, LLC...
The Issue: GE Healthcare has recently become aware of a potential safety issue to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z- GAS II EFFERVESCENT GRANULES Antacid/Antiflatulent Recalled by Bracco...
The Issue: Subpotent Drug: Out of Specification (OOS) result during routine stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcitonin ELISA Kit Recalled by Biomerica Due to A potential issue with...
The Issue: A potential issue with false high values.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number:...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.