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. 2,873 recalls have been distributed to Florida in the last 12 months.
Showing 12061–12080 of 55,837 recalls
Recalled Item: CENTURION SnagFree Chest Tube insertion Tray Recalled by MEDLINE INDUSTRIES,...
The Issue: One lot of chest tube insertion trays, containing a silk suture component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima Coil System Model Number OPTI0208CSS10 Recalled by BALT USA, LLC Due...
The Issue: Product pouch label does not match up with carton label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wisp and Wisp Youth Nasal Mask Recalled by Philips Respironics, Inc. Due to...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DreamWisp Nasal Mask with Over the Nose Cushion Recalled by Philips...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics Amara View Minimal Contact Full-Face Mask Recalled by...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR Patient Care Portal 5000 (Desktop Unit) Recalled by Philips North America...
The Issue: Device may intermittently fail to produce audio. Turning the unit off and on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Therapy Mask 3100 NC/SP Recalled by Philips Respironics, Inc. Due to No...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics DreamWear Full Face Mask Recalled by Philips...
The Issue: No contraindication/warning regarding magnetic components in CPAP masks for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clip COVID Rapid Antigen Test Kit (25-pack) Recalled by LUMINOSTICS, INC dba...
The Issue: COVID test kit shelf life was periodically extended, as real-time stability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Starling Monitor Recalled by Baxter Healthcare Corporation Due to Labeling...
The Issue: Labeling has incorrect or incomplete Unique Device Identification (UDI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy Hand Sanitizer Recalled by SUPERIOR GLOVE WORKS, LTD. Due to CGMP...
The Issue: CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Recreo Hair Growth Laser Comb Recalled by OMM Imports, Inc. dba Zero Gravity...
The Issue: The firm distributed the laser products without affixing the warning,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Surgical Level 3 Gown Recalled by Texas Medical Technology Inc....
The Issue: Surgical gowns recalled due to gown fabric failing to pass the hydrostatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introcan Safety FEP 14G Recalled by B Braun Medical Inc Due to Potential for...
The Issue: Potential for leakage at the catheter hub.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veritas Advanced Infusion Packs. Used in ophthalmic procedures. Recalled by...
The Issue: As a result of returned product complaints for Veritas Phaco packs related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydrochloride Jelly USP Recalled by Akorn, Inc. Due to cGMP...
The Issue: cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Ophthalmic Ointment USP Recalled by Akorn, Inc. Due to cGMP...
The Issue: cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MICRO-X ROVER MOBILE X-RAY SYSTEM Recalled by Micro-X Ltd. Due to Software...
The Issue: Software calibration error with product equip with a Dose Area Product (DAP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Antiserum to Human IgG Recalled by SIEMENS HEALTHCARE DIAGNOSTICS INC Due...
The Issue: N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.