Florida recalls
3970 federal recalls on file affecting Florida - 895 Florida-specific plus 3075 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-04FDA-DeviceNiproClass IINationwideStop using NIPRO Conductivity Standard Solution
due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for dialysate.
- 2026-02-04FDA-DeviceGold Star DistributionClass IINationwideStop using Gold Star Distribution pregnancy tests
Potential exposure of rodents and rodent activity in the distribution center.
- 2026-02-04FDA-DeviceGold Star DistributionClass IINationwideStop using recalled Oral-B and Colgate toothbrushes
Potential exposure of rodents and rodent activity in the distribution center.
- 2026-02-04FDA-DeviceGold Star DistributionClass IINationwideStop using recalled feminine hygiene products
Potential exposure of rodents and rodent activity in the distribution center.
- 2026-02-04FDA-DeviceGold Star DistributionClass IINationwideStop using recalled Trojan condoms
Potential exposure of rodents and rodent activity in the distribution center.
- 2026-02-04FDA-DeviceGold Star DistributionClass IINationwideStop using Gold Star first aid kits and bandages
Potential exposure of rodents and rodent activity in the distribution center.
- 2026-02-04FDA-DeviceCanonClass IINationwideCheck your Canon Medical X-ray system
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
- 2026-02-04FDA-DeviceCanonClass IINationwideCheck your Canon Medical X-ray system
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
- 2026-02-04FDA-DeviceCanonClass IINationwideContact Canon Medical about your Alphenix X-ray system
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
- 2026-02-04FDA-DeviceCanonClass IINationwideCheck your Canon Medical X-ray system
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
- 2026-02-04FDA-DeviceSiemensClass IINationwideContact Siemens about your LUMINOS Q.namix T system
Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.
- 2026-02-04FDA-DeviceSiemensClass IINationwideContact Siemens about your LUMINOS Q.namix R X-ray system
Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Aju Pharm AlternatiV+ anchors
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Aju Pharm AlternatiV+ Max anchors
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Aju Pharm suture anchors
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Genesis Knotless Anchor devices
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Genesis Dual Thread Screw-In Anchor
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Genesis Screw-In Anchor devices
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Aju Pharm Fixone Biocomposite Anchor
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
- 2026-02-04FDA-DeviceAju PharmClass IINationwideStop using Aju Pharm Fixone Hybrid Anchor
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
- 2026-02-04FDA-DeviceCerapedicsClass IINationwideCheck Cerapedics PearMatrix P-15 expiration dates
Incorrect expiration date
- 2026-02-04FDA-DeviceElektaClass IINationwideCheck your Elekta radiation therapy system
Due to a manufacturing issue and electrical grounding of systems.
- 2026-02-04FDA-DeviceSunMedClass INationwideStop using affected Broselow Tape units
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
- 2026-02-04FDA-DeviceSunMedClass INationwideStop using Broselow ALS Organizer model 7730ALS
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
- 2026-02-04FDA-DeviceSunMedClass INationwideStop using affected Broselow emergency tape
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
- 2026-02-04FDA-DeviceSunMedClass INationwideStop using SunMed Broselow emergency tape
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
- 2026-02-04FDA-FoodSuperfoodsClass INationwideStop using Live it Up Super Greens powder
Products may be contaminated with Salmonella Typhimurium
- 2026-02-04FDA-FoodSuperfoodsClass INationwideStop using Live it Up Super Greens powder
Products may be contaminated with Salmonella Typhimurium
- 2026-02-04FDA-FoodQuten Research InstituteClass IIStop using Qunol turmeric capsules
Mold contamination detected for raw material lots that were produced in July and used in finished goods.
- 2026-02-04FDA-DrugNovadozClass IIINationwideStop using recalled Novadoz glycopyrrolate solution
Failed Impurities/Degradation Specifications
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