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 · 3 months ago
Boston Scientific TheraSphere 360 Y-90 Management Platform recall: Software anomaly occurs when a user adds one or more vials to the cart
Software anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculator to modify one or more…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Olympus High Flow Insufflation Unit - UHI-4 recall: Potential for unexpected instances where the front panel display turns off
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Micro Therapeutics, Inc. Pipeline Flex Embolization Device with Shield Technology recall: Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants
Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Medline medical convenience kits labeled as: 1) KIT Pediatric Open recall: Medline Industries, LP is issuing a recall for specific Medline convenience
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Kent Imaging, Inc. SnapshotGLO Wound Imaging Device, Model KB100, KB100AA recall: The software controlling the wound imaging device's battery charging circuit
The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a battery that has fully…
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Class II · 3 months ago
AVID Medical, Inc. Halyard EYE PACK. Model/ recall: Incorrect concentration of Betadine solution contained within certain AVID
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
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Class II · 3 months ago
Wilcox Industries Corp recall: Wilcox is notifying all customers who have purchased a product from the BOSS
Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Paragon 28, Inc. P28 Phanton Intramedullary Nail System, Phantom Hindfoot TTC/TC Ball recall: Paragon 28 received two (2) complaints were received involving breaches
Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging.
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Class II · 3 months ago
Micro Therapeutics, Inc. Pipeline Flex Embolization Device with Shield Technology recall: Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants
Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants…
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Class II · 3 months ago
Medtronic Neurosurgery Ventriculostomy Kit, REF: 46154 recall: Ventriculostomy devices, used during ventriculostomy procedures to gain
Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed…
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Class II · 3 months ago
Medline medical convenience kits labeled as: 1) Total Joint Pack recall: Medline Industries, LP is issuing a recall for specific Medline convenience
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Medline medical convenience kits labeled as: 1) Shoulder Pack recall: Medline Industries, LP is issuing a recall for specific Medline convenience
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Ferno-Washington Inc Power F2 Powered Fastening System, Product No. 0567091 Powered recall: Product may experience accelerated roller wear and potential deformation
Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case…
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Class II · 3 months ago
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters 5cc recall: Affected kits contain recalled Bard Silastic Foley Catheters. Catheters
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present…
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Class II · 3 months ago
Karl Storz Endoscopy Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1 recall: Flexible hysteroscopes indicated for use during diagnostic and operative
Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal…
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Class II · 3 months ago
ICU Medical Inc. Hotline Fluid Warming Set, single use device recall: ICU Medical became aware of an increased likelihood of leakage in specific
ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate…
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Class II · 3 months ago
Medtronic MiniMed, Inc. MiniMed Go App, Model: MMT-8600 , MMT-8601 recall: For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night
For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the…