Recalls affecting Florida
Notices that name Florida in their distribution area, plus every nationwide recall — nationwide recalls reach Florida too.
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Class II · 10 months ago
Karabetian Import and Distribution, Inc. Product: Zimi Kunefe Ready to eat Package recall: partially hydrogenated oils (PHOs) in foods exported to the US
partially hydrogenated oils (PHOs) in foods exported to the US
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Class II · 10 months ago
Chips Ahoy Baked brownie bites recall: Product Safety – choking threats
Product Safety – choking threats
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Class II · 10 months ago
Gold Star Distribution All FDA-regulated products held at facility including drugs recall: Potential Salmonella contamination, presence of rodent and avian
Potential Salmonella contamination, presence of rodent and avian contamination and insanitary conditions during the storage process.
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Class I · 10 months ago
GE Medical Systems China Co., Ltd. GE Healthcare Carestation anesthesia system Power recall: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power…
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Class II · 10 months ago
Dsaart LLC Brand Name: AART Gluteal Implant Product Name: Gluteal Implant recall: Due to manufactured products that deviated from established specifications
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket…
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Class II · 10 months ago
Dsaart LLC Brand Name: AART Pectoral Implant Product Name: Pectoral Implant Model/ recall: Due to manufactured products that deviated from established specifications
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket…
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Class II · 10 months ago
DICOM Grid, Inc. Intelerad InteleShare software, with ProViewer component recall: Software intended to aid in diagnosing conditions
Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are…
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Class II · 10 months ago
Medline Industries, LP Forcep, STD STR, Sterile Kelly, 5.5 recall: The items may have weak packaging seals that may result in a breach
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if…
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Class II · 10 months ago
Copan Italia 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk recall: Treatment reagent functionality in respiratory specimens fluidification
Treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.
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Class II · 10 months ago
Medline Industries, LP Scissors, OR, Sharp/Blunt, 5.5", Sterile recall: The items may have weak packaging seals that may result in a breach
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if…
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Class II · 10 months ago
Medtronic MiniMed, Inc. InPen App, Model/CFN Number: MMT-8061 recall: When app is uninstalled and reinstalled, insulin pen software issue causes
When app is uninstalled and reinstalled, insulin pen software issue causes Choose Notification Style Screen to not show during setup so users can't…
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Class II · 10 months ago
Seaspine Orthopedics Corporation Orthofix NorthStar OCT Navigation Surgical Technique recall: The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly
The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards…
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Class II · 10 months ago
Dsaart LLC Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog recall: Due to manufactured products that deviated from established specifications
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket…
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Class II · 10 months ago
Cepheid Brand Name: Xpert¿ BCR-ABL Ultra Model/ recall: Invitro diagnostic test kits with specimens that have elevated white blood
Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results.
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Class I · 10 months ago
GE Medical Systems China Co., Ltd. GE Healthcare Carestation anesthesia system recall: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power…
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Class II · 10 months ago
Dsaart LLC Brand Name: AART Silicone Carving Implant Product Name: Silicone recall: Due to manufactured products that deviated from established specifications
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket…
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Class II · 10 months ago
Copan Italia 1ml of DTT in liquid phase, in PET tube with capture cap recall: Treatment reagent functionality in respiratory specimens liquification cannot
Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
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Class I · 10 months ago
Fresenius Kabi USA, LLC Ivenix Infusion System , LVP Software LVP-SW-0005. Software recall: Software version 5.10.1 and earlier contain anomalies that have the potential
Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death.
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Class III · 10 months ago
Datascope Corp. Cardiosave Hybrid recall: The IFU addendum updates the Vibration and Shock Table to reference
The IFU addendum updates the Vibration and Shock Table to reference the correct standards.
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Class II · 10 months ago
Dsaart LLC Brand Name: AART Malar Implant Product Name: Malar Implant Model/ recall: Due to manufactured products that deviated from established specifications
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket…
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Class II · 10 months ago
Dsaart LLC Brand Name: AART Calf Implant Product Name: Calf Implant Model/ recall: Due to manufactured products that deviated from established specifications
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket…
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Class I · 10 months ago
GE Medical Systems China Co., Ltd. GE Healthcare Carestation anesthesia system recall: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power…
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Class III · 10 months ago
Datascope Corp. Cardiosave Rescue recall: The IFU addendum updates the Vibration and Shock Table to reference
The IFU addendum updates the Vibration and Shock Table to reference the correct standards.
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Class II · 10 months ago
Abbott Laboratories Alinity ci-series System Control Module , REF: 03R70-01, 03R70-20 recall: Abbott Laboratories is recalling their Alinity ci-series System Control
Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction. The reason for the…