State

Oregon product recalls

72,992 recalls have nationwide distribution and so reach Oregon. 7,526 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total: 7,526
Critical: 876
Severe: 1,803
Most recent: 2026-09-16

Of the 7,526 recalls naming Oregon we have scored against our rubric, 876 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,803 (24%) are Severe.

Which agencies issued them

These figures cover only the 7,526 recalls whose distribution notice names Oregon specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8526–8550 of 80518

HighFDA (Devices)·Z-0797-2025·2025-01-08
3M Unitek Orthodontic Primer Recalled Due to Bond Failures and Skin Irritation
3M Unitek is recalling Transbond Plus Self-Etching Primer used in orthodontic bonding due to reports of bracket bond failures and skin irritation or blistering.
Product
3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self Etching Primer is an orthodontic all-in-one etchant and primer that is used in the bonding process of orthodontic appliances to teeth.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0789-2025·2025-01-08
Medline MICRODISECTOMY PACK recalled for endotoxin contamination
Medline custom MICRODISECTOMY PACK kits containing non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination are being recalled. Approximately 1,494 units were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) MICRODISECTOMY PACK, REF DYNJ80585A; 2) MICRODISECTOMY PACK, REF DYNJ80585B.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0779-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Non-Sterile Components
Medline is recalling custom surgical procedure kits containing non-sterile surgical components with potential endotoxin contamination. The recall affects 1,402 units distributed in the US, Canada, and UAE.
Product
Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS, REF CDS983470D; 2) 1/2X1/2 NEURO SPONGE PACK-LF, REF DYNJ0713177; 3) BURR HOLE SHUNT PACK, REF DYNJ56819D; 4) BURR HOLE SHUNT PACK, REF DYNJ56819F; 5) BURR HOLE SHUNT PACK, REF DYNJ56819G; 6) RO VP SH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0780-2025·2025-01-08
Medline custom surgical procedure kits recalled for non-sterile components and endotoxin contamination
Medline custom procedure kits containing non-sterile Codman Surgical Patties & Strips are being recalled due to potential endotoxin contamination. The recall affects 74 units distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER SUPPLEMENT, REF DYNJ69476; 2) DIEP FLAP, REF DYNJ910120
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0782-2025·2025-01-08
Medical Device Kits Recalled for Non-Sterile Surgical Components
Medline Industries is recalling See DocMan custom convenience kits that contain non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. Approximately 48,655 units were distributed worldwide.
Product
See DocMan
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0321-2025·2025-01-08
An Pan Buns Lack Sesame Allergen Declaration on Label
Oyatsupan Bakers is recalling An Pan buns because the allergen declaration doesn't list sesame, though black sesame seeds are visible and listed in ingredients. Distribution was limited to Oregon and Washington.
Product
An Pan bun is a sweet roll filled with sweet red bean paste, stamped with black sesame seeds on top. Product is packaged in clear polypropylene bag, heat sealed with white labels on front and back. Net wt. 2.9pz. UPC 854077007055. The affected label states "**INGREDIENTS: Azuki
Category
Food
Distribution
2 states
HighNHTSA·25V003000·2025-01-08
Blue Bird Recalls 2024-2025 All American School Buses for Wiring Defect
Blue Bird is recalling 2024-2025 All American school buses because incorrect wiring reverses high and low beams, potentially blinding other drivers.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0771-2025·2025-01-08
Medtronic SynchroMed II and III Implantable Pumps Recalled for Software Defects
Medtronic is recalling SynchroMed II and III implantable pumps used with a clinician tablet app that has software issues in version 2.x. Approximately 319 systems were distributed worldwide.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2.x, CFN CT900B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0790-2025·2025-01-08
See DocMan Surgical Kits Recalled for Non-Sterile Surgical Patties and Strips
Medline Industries is recalling See DocMan custom convenience kits containing non-sterile Codman Surgical Patties and Strips due to potential endotoxin contamination.
Product
See DocMan
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0775-2025·2025-01-08
Baxter SIGMA Spectrum Infusion Pump Recalled for Incomplete Post-Repair Testing
Baxter is recalling SIGMA Spectrum Infusion Pump (Version 6) units that were released after repair without complete flow testing. The incomplete testing poses a risk of improper device operation.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0793-2025·2025-01-08
Medline custom surgical procedure kits recalled for non-sterile components
Medline is recalling 182 custom surgical procedure kits containing non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. The kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) CERVICAL PACK-LF, REF DYNJ0867145G; 2) CERVICAL SPINE PACK HUM-LF, REF DYNJ35184F; 3) ANTERIOR CERVICAL-CORPECTOMY, REF DYNJ904827.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0774-2025·2025-01-08
SynchroMed II and III Implantable Pumps Recalled for Software Issues
Medtronic has recalled 3,981 SynchroMed implantable pumps worldwide due to software issues in application version 2.x used to program the devices.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900E CLINICIAN TABLET GLBL SMSNG and PROG CT900E CLINICIAN TABLET PAPER EN with the A810 CP app version 2.x, CFN CT900E
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·25088·2025-01-08
Children's Bike Helmets Recalled for Failure to Meet Federal Safety Standards
About 6,500 Wemfg children's bike helmets sold on Amazon fail to comply with federal safety standards for impact protection and stability. The helmets can fail to protect in crashes, posing a risk of head injury.
Product
Wemfg Children's Multi-Purpose Bike Helmets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25087·2025-01-08
SIG SAUER ROMEO5 Red Dot Firearm Sights Recalled Due to Button Battery Ingestion Hazard
SIG SAUER recalled about 230,000 ROMEO5 red dot sights because the included button cell battery can be easily accessed and lacks required child-resistant packaging, posing a serious ingestion hazard to children.
Product
SIG SAUER ROMEO5 Red Dot Sights
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0172-2025·2025-01-08
Dapsone Topical Gel Recalled Due to Crystallization Defect
Viona Pharmaceuticals is recalling Dapsone Gel 7.5% (2760 packs) distributed nationwide due to crystallization in the formulation. The voluntary recall affects lots T400514 and T400808.
Product
DAPSONE — DAPSONE (DAPSONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0778-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Endotoxin Contamination Risk
Medline Industries is recalling 2344 custom surgical kits with non-sterile components that may contain endotoxins. The kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF, REFCDS840451M; 2) NEURO PACK, REFDYNJ41516M; 3) RFD- AAA PACK, REFDYNJ54242B; 4) OPEN HEART A&B, REFDYNJ901203C; 5) OPEN HEART A&B, REFDYNJ901203D; 6) ACDF-LF, REFDYNJ906681B; 7) ACDF-LF, REFDY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0773-2025·2025-01-08
Medtronic Implantable Drug Pumps Recalled for Software Defects
Medtronic has recalled 566 SynchroMed II and III implantable drug infusion pumps due to software issues in the controlling application. No injuries or illnesses have been reported.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V004000·2025-01-08
Blue Bird Recalls 2025 All American Bus for Wiring Defect
Blue Bird is recalling one 2025 All American transit bus because incorrect wiring reverses high and low beams, potentially blinding other drivers.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0776-2025·2025-01-08
Baxter Infusion Pump Recalled for Incomplete Post-Repair Testing
Baxter Healthcare is recalling certain infusion pumps that were released after repair without complete testing. Incomplete testing could affect how the device delivers medication to patients.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0365-2025·2025-01-08
Sam's Club Hatch Chile Chicken Enchiladas Recalled for Listeria
Sam's Club is recalling Member's Mark Hatch Chile Chicken Enchiladas because the product may contain Listeria monocytogenes.
Product
Member's Mark Hatch Chile Chicken Enchiladas, ready to cook, perishable, packaging type: aluminum/black oven-safe tray Net wt. variable - average 1.52 lbs. UPC 00226529000004, UPC 00409802813793
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0784-2025·2025-01-08
Medline Custom Surgical Procedure Kits Recalled for Potential Endotoxin Contamination
Medline Industries is recalling custom medical procedure kits due to non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. Approximately 1,072 units were distributed in the US, Canada, and UAE.
Product
Medline custom medical procedure kits labeled as: 1) ENDOSCOPIC SKULL BASE, REF DYNJ58648B; 2) ENDOSCOPIC SKULL BASE, REF DYNJ58648C; 3) ENT ENDO SINUS WILMINGTON PACK, REF DYNJ66447; 4) ENDOSCOPIC SKULL BASE, REF DYNJ58648D; 5) ENDOSCOPIC SKULL BASE, REF DYNJ58648J.
Category
Medical Device
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-01082025-01·2025-01-08
Chicken Curry Empanadas Recalled For Undeclared Milk Allergen
USDA FSIS issued a public health alert for Chicken Curry Empanadas that may contain undeclared milk. Consumers with milk allergies should not consume these products.
Product
Rajbhog Foods (NJ), Inc. — FSIS Issues Public Health Alert For Chicken Empanada Products Due To Misbranding And Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0770-2025·2025-01-08
Auryon Laser Atherectomy System Recalled for Activation Failure
Angiodynamics is recalling 138 units of the Auryon atherectomy laser system due to potential failure to advance to activation mode during use. This malfunction could cause procedural delays or interruptions.
Product
AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0171-2025·2025-01-08
Dapsone Gel Recalled Nationwide for Crystallization
Viona Pharmaceuticals is recalling Dapsone Gel 7.5% nationwide due to crystallization detected in multiple lots. Patients should contact their pharmacy or healthcare provider for guidance.
Product
DAPSONE — DAPSONE (DAPSONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0168-2025·2025-01-08
AvKARE Nitrofurantoin 100 mg Capsules Recalled for Dissolution Failures
AvKARE is recalling Nitrofurantoin 100 mg capsules (NDC 50268-625-15, lot 47101, exp. 02/2026) nationwide because they failed dissolution specifications. Affected users should consult their healthcare provider.
Product
Nitrofurantoin Capsules, USP, 100 mg, 50 Capsules (5 x 10) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478. NDC#: 50268-625-15.
Category
Drug
Distribution
Distributed nationwide