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. 2,939 recalls have been distributed to Florida in the last 12 months.
Showing 1561–1580 of 55,837 recalls
Recalled Item: Allura Xper FD10/10 Product Codes: (1)722011 Recalled by PHILIPS MEDICAL...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/15 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 OR Table Product Codes: (1)722022 Recalled by PHILIPS...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura CV20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Product Codes: (1)722010 Recalled by PHILIPS MEDICAL...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 OR Table Product Codes: (1)722023 Recalled by PHILIPS...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane OR Table Product Codes: (1)722020 Recalled by...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Product Codes: (1)722012 Recalled by PHILIPS MEDICAL...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Systems may not perform as intended due to the deterioration of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norgestimate and Ethinyl Estradiol Tablets Recalled by AvKARE Due to Failed...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Recalled by The Harvard Drug Group LLC dba...
The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Recalled by The Harvard Drug Group LLC dba...
The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tribio Implant 7.5mm x 40mm SB008 UDI code: Recalled by Berkeley Advanced...
The Issue: Due to incorrect product label (Incorrect product name identified on outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artegraft Collagen Vascular Grafts Model Numbers: (1) AG 616 Recalled by...
The Issue: The bovine carotid arteries used to produce the impacted grafts from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rolling Pin brand Dubai Style Chocolate Recalled by ROLLING PIN BAKING...
The Issue: Product does not declare wheat in the allergen statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: bevacizumab (Avastin) Injection Recalled by Fagron Compounding Services Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLEARLINK System Solution Set Recalled by Baxter Healthcare Corporation Due...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK SYSTEM CONTINU-FLO Solution Set Recalled by Baxter Healthcare...
The Issue: IV sets may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.