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. 2,918 recalls have been distributed to Florida in the last 12 months.
Showing 5221–5240 of 30,686 recalls
Recalled Item: RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement....
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7514...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DUR PCA MTK REV INS RT Intended for knee replacement Recalled by Howmedica...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P7 28MM 10 DEGREE +4MM INSERT Intended for knee replacement Recalled by...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips North America Due to While using...
The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bkActiv Ultrasound System 2300 Recalled by B-K Medical A/S Due to An issue...
The Issue: An issue on the Dual Live Compare feature on the bkActiv system could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Link Patella Glide Resection Guide- For the implantation of the Recalled by...
The Issue: Mislabeled: Angle and height of the device marked as L(large) corresponds to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GammaPod - Treatment Planning System-a component of the GammaPod Irradiation...
The Issue: Wrong structures imported into the GammaPod Treatment Planning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT 7500 Recalled by Philips North America Llc Due to Multiple...
The Issue: Multiple software issues that affect device functionality.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips North America Due to While using...
The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Recalled by Philips North America Due to While using...
The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Model 3120 ZOOM LATITUDE Programmer/Recorder/Monitor (PRM)...
The Issue: The software application on the Programmer/Recorder/Monitor (PRM) for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnipod 5 App (on compatible Android smartphones) Recalled by Insulet...
The Issue: The bolus calculator is not recording the decimal point if it is the first...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 9251R1 Recalled by Busse Hospital Disposables, Inc. Due to Firm...
The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 1443 DRESSING CHANGE TRAY / STERILE - LATEX FREE Recalled by...
The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE Recalled by...
The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe Hemo Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility of the Sensis documentation functionality application to crash.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.