Florida recalls
1541 federal recalls on file affecting Florida - 129 Florida-specific plus 1412 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-04-01FDA-DeviceGEClass IINationwideStop using affected GE Imactis CT-Navigation systems
There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position.
- 2026-04-01FDA-DeviceNavajo ManufacturingClass INationwideStop using Handy Solutions heating pad model 25607
If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad under the body, then the high limit device is unable to sense the higher temperature so power is not terminated. May cause a burning smell prior to melting/burning potentially causing burns to persons and property.
- 2026-04-01FDA-DeviceMerit MedicalClass INationwideStop using Merit Medical BioFlo DuraMax Catheter
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.
- 2026-04-01FDA-DeviceMerit MedicalClass INationwideStop using Merit Medical DuraMax catheters
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.
- 2026-04-01FDA-DeviceMerit MedicalClass INationwideStop using Merit Medical 16F sheath introducer
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.
- 2026-04-01FDA-DeviceMerit MedicalClass INationwideStop using Merit Medical ProGuide dialysis catheters
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.
- 2026-04-01FDA-DeviceMerit MedicalClass INationwideStop using Merit Medical CentrosFLO catheters
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.
- 2026-04-01FDA-DeviceErbeClass INationwideStop using Erbe USA Flexible Cryoprobe
Probes may rupture/burst during activation
- 2026-04-01FDA-DeviceErbeClass INationwideStop using Erbe USA Flexible Cryoprobe devices
Probes may rupture/burst during activation
- 2026-04-01FDA-DeviceErbeClass INationwideStop using Erbe USA cryoprobes immediately
Probes may rupture/burst during activation
- 2026-04-01FDA-FoodNuts.comClass INationwideStop eating Nuts.com Espresso Malted Milk Balls
Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy.
- 2026-04-01FDA-FoodSouth Florida FoodClass IIDo not eat South Florida Food Pan de Bono
Undeclared Soy.
- 2026-04-01FDA-FoodBakkavorClass IIDiscard roasted tomato parmesan focaccia bread
Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
- 2026-04-01FDA-FoodBakkavorClass IIStop eating Bakkavor basil pesto pizza
Metal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by one of their ingredient suppliers.
- 2026-04-01FDA-FoodAmerican LaboratoriesClass IIStop using American Laboratories Pepsin powder
Potential Salmonella contamination.
- 2026-04-01FDA-FoodAmerican LaboratoriesClass IIStop using American Laboratories pepsin powder
Potential Salmonella contamination.
- 2026-04-01FDA-FoodAmerican LaboratoriesClass IIStop using American Laboratories Pepsin powder
Potential Salmonella contamination.
- 2026-04-01FDA-FoodHerbal Creations USAClass IINationwideBulk packaged Colustrum Powder. packaged with generic product label.
Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.
- 2026-04-01FDA-FoodWestern MixersClass IINationwideStop using Treasured Harvest Chilli Spanish Peanuts
Foreign object (glass) found inside sealed container of finished product.
- 2026-04-01FDA-FoodWestern MixersClass IINationwideStop eating First Street Chilli Spanish Peanuts
Foreign object (glass) found inside sealed container of finished product.
- 2026-04-01FDA-DrugAmerisourceClass IINationwideStop using recalled Meclizine Hydrochloride tablets
Failed tablet specifications.
- 2026-04-01FDA-DrugTevaClass IINationwideStop using recalled Teva Octreotide Acetate injections
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
- 2026-04-01FDA-DrugTevaClass IINationwideStop using Teva Octreotide Acetate injections
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
- 2026-04-01FDA-DrugTevaClass IINationwideStop using Teva Octreotide Acetate injection
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
- 2026-04-01FDA-DrugMacLeods PharmaClass IINationwideStop using Macleods Pharma levothyroxine tablets
Subpotent Drug
- 2026-04-01FDA-DrugChiesiClass IINationwideStop using recalled CUROSURF lung surfactant
Lack of Assurance of Sterility
- 2026-04-01FDA-DrugRadnostixClass IIINationwideStop using Radnostix Gelatin Capsule Pack
Failed Tablet/Capsule Specifications
- 2026-03-30FDA-PRBuy-herbal.comNationwideStop using Kian Pee Wan capsules immediately
FOR IMMEDIATE RELEASE – 03/30/2026 - Flushing, New York, Aphreseller (Ebay seller ID), Buy-herbal.com is recalling all lots of Kian Pee Wan capsules to the consumer level. FDA analysis has found that the product contains the undeclared drug ingredients dexamethasone and cyproheptadine. Products cont
- 2026-03-26CPSCBioenrrtyNationwideStop using MPINOI bed rails immediately
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail, or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.
- 2026-03-26CPSCDIY Cold PlungeNationwideStop using DIY Cold Plunge Sauna Heater Kit
Electrical conductors within the sauna heater kits can overheat, posing a fire hazard and risk of serious injury or death.
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