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. 2,723 recalls have been distributed to Florida in the last 12 months.
Showing 25301–25320 of 55,837 recalls
Recalled Item: smith&nephew SMF(TM) STANDARD OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1...
The Issue: Complaints were received indicating that the outer label incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive...
The Issue: Deterioration of C-reactive protein (CRP) reagent in Optilite C-Reactive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew SMF(TM) HIGH OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1H...
The Issue: Complaints were received indicating that the outer label incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Knife 5.0mm 30¿ Recalled by Beaver Visitec Due to The product contains...
The Issue: The product contains a misprinted expiration date on the peel pack. Both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with the following systems: 722001 Allura Xper Recalled...
The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector...
The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to Recalled by Avitus...
The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to Recalled by Avitus...
The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concord Fresh Success Mild Salsa Seasoning Mix Recalled by Concord Foods,...
The Issue: Product contains undeclared allergen, milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nature's Path Organic Cinnamon Jungle Munch cereal. Net Wt. 10 oz (284 g)...
The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nature's Path Organic Gorilla Munch Corn Puffs cereal. Net Wt. 10 oz (284 g)...
The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nature's Path Organic Chocolate Choco Chimps Organic cereal. Net Wt....
The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alere Cholestech LDX Analyzer Recalled by Alere San Diego, Inc. Due to The...
The Issue: The polarity of the output of power supply was reversed. Due to polarity of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickTox 5 Panel Drug Screen DipCard Recalled by Ameditech Inc Due to Mixed...
The Issue: Mixed Products containing QuickTox 5 Panel Drugs Screen Dipcard (P/N QT11,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Force TriVerse electrosurgical device 10 cord-Intended as...
The Issue: Potential for the sterile packaging to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etomidate Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...
The Issue: Subpotent Drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimercaptopropanesulfonate Sodium (DMPS) Recalled by McGuff Compounding...
The Issue: Presence of Particulate Matter: Particulates observed in vials release for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane...
The Issue: Complaints received that products packaged with the incorrect introducer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.