Recalls affecting Oregon
Notices that name Oregon in their distribution area, plus every nationwide recall — nationwide recalls reach Oregon too.
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Class II · 10 months ago
Merck Sharp & Dohme LLC Noxafil Powdermix for Delayed-Release Oral Suspension, 300 mg recall: Presence of particulate matter: potential presence of metal particulates
Presence of particulate matter: potential presence of metal particulates in the product.
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Class II · 10 months ago
Merck Emend for oral suspension, 125 mg, Single-Dose Kit recall: Presence of particulate matter: potential presence of metal particulates
Presence of particulate matter: potential presence of metal particulates in the product.
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Class I · 10 months ago
Carousel Candies Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz recall: Undeclared pecan
Undeclared pecan
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Class I · 10 months ago
Carousel Candies Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pouch Bag recall: Undeclared wheat
Undeclared wheat
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Class II · 10 months ago
Karabetian Import and Distribution, Inc. Product: Zimi Puff Pastry French Style 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
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
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
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 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 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 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…
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Class II · 10 months ago
Myofunctional Research Company USA Myosa for Kids KS1 REF MyOsaks1_Sb/Sp/Mb/Mp/Lb/Lc recall: Due to firm mistakenly distributing product within the U.S. without FDA
Due to firm mistakenly distributing product within the U.S. without FDA premarket clearance/approval.
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Class II · 10 months ago
Mindray North America Hardware configuration of the BeneVision Central Monitoring recall: When the Worstation of the BeneVision DMS has a specific hardware
When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen…
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Class II · 10 months ago
Smith & Nephew, Inc. Biosure HA Screw, 6MM x 20 MM. Threaded metallic bone fixation recall: Removal of affected lot of screws due to labeling error
Removal of affected lot of screws due to labeling error.
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Class II · 10 months ago
Novocol Pharmaceutical of Canada, Inc. Lidocaine HCI 2% and Epinephrine 1:100,000 recall: Defective container: cracked/broken cartridges
Defective container: cracked/broken cartridges