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
Windstone Medical Packaging, Inc. AMS Aligned Medical Solutions medical convenience recall: Windstone Medical Packaging recalled specific items and lots of AMS
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…
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Class II · 3 months ago
Windstone Medical Packaging, Inc. AMS Aligned Medical Solutions medical convenience recall: Windstone Medical Packaging recalled specific items and lots of AMS
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…
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Class III · 3 months ago
Ascend Laboratories, LLC Dabigatran Etexilate Capsules, 150 mg recall: Failed impurity/degradation specification: an OOS result observed in Related
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total…
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Class II · 3 months ago
Micro Labs USA Inc Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP recall: Defective Container: Firm received multiple complaints of broken cap spikes
Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.
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Class II · 3 months ago
Mylan Pharmaceuticals Inc Mycophenolate Mofetil for Injection USP, 500 mg/Vial recall: Presence of precipitate
Presence of precipitate
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Class II · 3 months ago
Glenmark Pharmaceuticals Inc., USA Azelaic Acid Gel, 15%, 50 gram tubes recall: CGMP Deviations: Product quality complaints concerning abnormal texture
CGMP Deviations: Product quality complaints concerning abnormal texture or consistency (described as grainy, gritty, or sandy) were received.
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Class III · 3 months ago
Ascend Laboratories, LLC Dabigatran Etexilate Capsules, 75 mg recall: Failed impurity/degradation specification: an OOS result observed in Related
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total…
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Class III · 3 months ago
Ascend Laboratories, LLC Dabigatran Etexilate Capsules, 75 mg recall: Failed impurity/degradation specification: an OOS result observed in Related
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total…
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Class II · 3 months ago
Mellish Island Super Skin recall: Firm's finished product label does not declare the source of marine collagen
Firm's finished product label does not declare the source of marine collagen which was determined to be fish.
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NHTSA safety recall · 3 months ago
General recall: The high voltage battery may have an improperly secured internal module
The high voltage battery may have an improperly secured internal module component.
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Highest risk · 3 months ago
Jake's Fireworks World Class Fireworks "Skull Strobe" Rockets recall: Risk of Serious Injury from Explosion and Burn Hazards
Risk of Serious Injury from Explosion and Burn Hazards
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Highest risk · 3 months ago
Golden Link Fantastic Four Cups and Captain America Popcorn Helmet Containers recall: Risk of Serious Injury or Death from Battery Ingestion Hazard
Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
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Highest risk · 3 months ago
Galanz Americas Retro Refrigerators recall: Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported
Risk of Serious Injury or Death from Fire and Burn Hazards; One Death Reported
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Public Health Alert · 3 months ago
Mary's Harvest Fresh Foods, Inc. Public Health Alert for Chicken Salad products recall: Product Contamination
Product Contamination
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Class II · 3 months ago
Olympus 4K UHD LCD Monitor recall: Potential for the HDMI and DisplayPort (DP) connectors can become faulty
Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.
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Class II · 3 months ago
Boston Scientific Corporation Faradrive Steerable Sheath - US recall: Boston Scientific's complaint investigations have identified that a subset
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage…
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Class II · 3 months ago
Boston Scientific Corporation Faradrive Steerable Sheath Clear IDE recall: Boston Scientific's complaint investigations have identified that a subset
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage…
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Class II · 3 months ago
Medline medical convenience kits labeled as: Neuro 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
Prismatik Dentalcraft, Inc. Brand Name: Silent Nite Product Name: Silent Nite Sleep recall: Due to device not having FDA Clearance
Due to device not having FDA Clearance
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Class II · 3 months ago
PIE Medical Imaging B.V. 3mensio Workstation software recall: User measurement value reported by diagnostic bioimaging software intended
User measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to…
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Class II · 3 months ago
SeaSpine Polyaxial Head REF Number: 41-3010 recall: Due to manufacturing error, polyaxial head may popoff from the screw
Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
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Class II · 3 months ago
Boston Scientific Corporation Faradrive Steerable Sheath Clear OUS recall: Boston Scientific's complaint investigations have identified that a subset
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage…
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Class II · 3 months ago
Emano Flow with software version v2.0.0 GS1 GTIN code: 199874903484 recall: Problem description/Reason for recall: During the period March 22, 2026
Problem description/Reason for recall: During the period March 22, 2026, to May 29, 2026, recorded urination audio was captured at 48,000 Hz while…
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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…