State

Oregon product recalls

72,936 recalls have nationwide distribution and so reach Oregon. 7,525 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total: 7,525
Critical: 876
Severe: 1,803
Most recent: 2026-09-09

Of the 7,525 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 7,525 recalls whose distribution notice names Oregon specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3126–3150 of 80461

HighCPSC·26306·2026-02-26
Andersen Windows Recalls Window Opening Control Devices on 100 Series Casement Windows
Andersen Windows is recalling about 91,000 window opening control devices sold as kits or installed on 100 Series casement windows because they can break or detach after impact, posing fall and serious injury hazards. No injuries have been reported.
Product
Window opening control devices sold as kits or installed on 100 Series casement windows
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26295·2026-02-26
TheKiddoSpace Recalls Reusable Water Balloons Over Phthalate Ban Violation
TheKiddoSpace is recalling about 4,300 reusable water balloons because the cord lock on the storage bag contains a regulated phthalate that violates the federal phthalate ban. No injuries have been reported.
Product
TheKiddoSpace Reusable Water Balloons
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26305·2026-02-26
SumDirect LED Mini Lights Recalled Over Battery Ingestion Hazard
SumDirect LED Mini Lights are recalled because the button cell batteries can be easily accessed by children, posing an ingestion hazard. No injuries have been reported.
Product
SumDirect LED Mini Lights
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26292·2026-02-26
TheKiddoSpace Recalls Children's Story Books Due to Choking Hazard
TheKiddoSpace is recalling about 140 children's story books because felt parts can detach and pose a choking hazard. No injuries have been reported.
Product
TheKiddoSpace Children's Story Books
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·26V115000·2026-02-26
BMW Recalls One 2026 S 1000 RR Motorcycle for Turn Signal Defect
BMW is recalling one 2026 S 1000 RR motorcycle because the turn signal reset button can be unintentionally activated, causing the turn signal to fail.
Product
BMW — BMW S 1000 RR
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·26289·2026-02-26
Magnetic Chess Games Recalled Over Magnet Ingestion Risk
Magnetic chess games sold on Amazon by Kaiwenshangpin are recalled because loose magnets inside can be swallowed by children, potentially causing intestinal damage or death. No injuries have been reported.
Product
Magnetic Chess Games
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26264·2026-02-26
Vevor Retractable Baby Gates Recalled Due to Entrapment Hazard
Sanven Technology is recalling approximately 10,400 Vevor Retractable Baby Gates because they violate safety standards and pose an entrapment risk to children.
Product
Vevor Retractable Baby Gates
Category
Consumer Product
Distribution
Distributed nationwide
ModerateNHTSA·26V114000·2026-02-26
General Motors Vehicles Recalled for Missing Electronic Owner's Manual
General Motors has recalled multiple Chevrolet, GMC, Cadillac, and Buick vehicles from 2025–2027 because their radios were not properly configured to download the electronic owner's manual during production. Without the manual, owners may not know how to safely operate the vehicle.
Product
CHEVROLET — CHEVROLET, CADILLAC, BUICK SILVERADO 2500, SILVERADO 3500, BLAZER EV, VISTIQ
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1353-2026·2026-02-25
Olympus High Flow Insufflation Unit Model UHI-2 Recalled Due to Software Issue
Olympus Corporation of the Americas is recalling 744 Olympus High Flow Insufflation Units (Model UHI-2) because a software algorithm issue may cause overpressure events.
Product
Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to facilitate laparoscopic observation and treatment within the abdominal cavity.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0510-2026·2026-02-25
Moringa capsules recalled over potential contamination with Salmonella
Art Monkey LLC is recalling 8,500 bottles of Why Not Natural Moringa Capsules because they have the potential to be contaminated with Salmonella.
Product
Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the bottom and with an expiration date of 07/2028 stamped on the bottom.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1352-2026·2026-02-25
Olympus High Flow Insufflation Unit Recalled Due to Software Algorithm Issue
Olympus Corporation of the Americas is recalling the Olympus High Flow Insufflation Unit (Model UHI) because a software algorithm issue may cause overpressure events.
Product
Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to facilitate laparoscopic observation and treatment within the abdominal cavity.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1354-2026·2026-02-25
Olympus High Flow Insufflation Unit Recalled Due to Software Overpressure Risk
Olympus is recalling 485 High Flow Insufflation Units (Model UHI-3) nationwide due to a software algorithm issue that may cause dangerous overpressure during abdominal surgery.
Product
Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to facilitate laparoscopic observation and treatment within the abdominal cavity.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1382-2026·2026-02-25
Olympus Thunderbeat Surgical Device Recall Over Adverse Events
Olympus is recalling 1,538 Thunderbeat 5 mm surgical devices worldwide due to continued reports of adverse events. The recall affects all units of Model No. TB-0510IC.
Product
Olympus Thunderbeat 5 mm, 10 cm, Inline Grip
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1415-2026·2026-02-25
Medline Recalls Surgical Convenience Kits Over Sterilization Calibration Issues
Medline is recalling 12,418 units of various surgical convenience kits due to calibration issues with equipment used for sterilization and packaging, which may affect the sterility assurance level of the devices.
Product
Medline Convenience Kits: 1) ROBOTIC GYN CDS-1, Model Number: CDS982893I; 2) GYN LAPAROSCOPY CDS, Model Number: CDS983300J; 3) NHP ROBOTIC GYNE CDS, Model Number: CDS984243G; 4) ROBOTIC-LF, Model Number: CDS984543D; 5) ROBOTIC-LF, Model Number: CDS984543F; 6) ROBOTIC-L
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1385-2026·2026-02-25
Medline Tracheostomy Convenience Kits Recalled Over Sterilization Calibration Concerns
Medline is recalling 753 units of its tracheostomy convenience kits and trach tote due to potential sterilization equipment calibration issues that may affect the sterility assurance level of the devices.
Product
Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY, Model Number: DYKMBNDL55; 2) KIT STC TRACHEOSTOMY, Model Number: DYKMBNDL55A; 3) TRACH TOTE, Model Number: DYNJ85691
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1365-2026·2026-02-25
Integra CVS Wound Dressing Recall Over Sterile Barrier Breach Risk
Integra LifeSciences is recalling 2,906 units of its Private Label CVS wound dressings (Model CVS405406) due to potential packaging failures that could compromise the sterile barrier.
Product
Private Label CVS. Model Number: CVS405406. Helps maintain a moist wound environment, which has shown to be conducive to wound healing. Intended for minor scalds & burns, minor cuts, lacerations & minor abrasions.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1371-2026·2026-02-25
Olympus Thunderbeat Surgical Device Recall Due to Adverse Events
Olympus is recalling 9,542 Thunderbeat surgical devices worldwide due to continued reports of adverse events. The recall affects all lots of the TB-0545FCS model.
Product
Olympus Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1414-2026·2026-02-25
Medline Labor and Delivery Convenience Kits Recalled Over Sterilization Calibration
Medline is recalling 27,320 labor and delivery convenience kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the devices.
Product
Medline Convenience Kits: 1) OB KIT, Model Number: DYKM2326; 2) KIT LABOR DELIVERY TUBAL LIGAT, Model Number: DYKMBNDL165; 3) KIT LABOR & DELIVERY D&C/D&E, Model Number: DYKMBNDL31; 4) KIT LABOR & DELIVERY CERCLAGE, Model Number: DYKMBNDL38; 5) L & D PACK-LF, Model Numbe
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1404-2026·2026-02-25
Medline Burn Care Kits Recalled Over Sterilization Calibration Issues
Medline is recalling 291 units of three burn care convenience kits due to calibration issues with sterilization and packaging equipment that may affect sterility assurance.
Product
Medline Convenience Kits: 1) BURN PACK, Model Number: DYNJ15668R; 2) BURN PACK-LF, Model Number: DYNJ42829B; 3) BURN CARE PACK-LF, Model Number: DYNJT3437
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1397-2026·2026-02-25
Medline Sterile Surgical Kits Recalled Over Sterilization Equipment Calibration
Medline is recalling 4,757 units of convenience surgical kits distributed worldwide due to calibration issues with sterilization and packaging equipment that may affect sterility assurance.
Product
Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS, Model Number: ACC010499; 2) KIT UROLOGY URETHROPLASTY, Model Number: DYKMBNDL117C; 3) KIT PLASTIC INSERT TISSUE EXPA, Model Number: DYKMBNDL158; 4) KIT PLASTIC ABDOMINOPLASTY, Model Number: DYKMBNDL170; 5) KIT PLASTIC
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1387-2026·2026-02-25
Medline Nerve Block Trays Recalled Over Sterilization Calibration Issues
Medline is recalling 448 units of its BASIC NERVE BLOCK TRAY W/LINEN (Model PAIN0150C) due to calibration issues with sterilization and packaging equipment that could affect the sterility assurance level of the devices.
Product
Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN, Model Number: PAIN0150C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1366-2026·2026-02-25
Medline Industries IV Administration and Extension Sets Recalled Due to Potential Leaks
Medline Industries, LP is recalling various IV administration and extension sets because male luer connectors may leak, crack, or break during use.
Product
Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET,60DRP,1NEEDLE-FREE VALV, Model Number: DYNDTB0529; 2) IV ADMIN SET, 10DRP, 1NF, 92, Model Number: DYNDTB1029; 3) DBD-IVEXTSET2.4ML2 NEEDLE-FREEVLVE,35, Model Number: DYNDTB1516; 4) DBD-IV ADMIN SE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1402-2026·2026-02-25
Driveline and central venous kits recalled over sterilization calibration issues
Medline is recalling 684 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Product
Medline Convenience Kits: 1) LVAD DRIVELINE TRAY, Model Number: DM1035; 2) KIT SURG ONC INSERT CENT.VENOU, Model Number: DYKMBNDL43
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1380-2026·2026-02-25
Olympus Thunderbeat 5 mm 35 cm Inline Grip Medical Device Recall
Olympus Corporation of the Americas is recalling Olympus Thunderbeat 5 mm, 35 cm, Inline Grip devices due to reports of adverse events.
Product
Olympus Thunderbeat, 5 mm, 35 cm, Inline Grip
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1406-2026·2026-02-25
Choice drape packs recalled over sterilization equipment calibration issues
Medline is recalling 72 units of convenience kits because calibration issues with the equipment used to sterilize and package them may affect the sterility assurance level.
Product
Medline Convenience Kits: 1) DRAPE PACK-CHOICE, Model Number: DYNJ63118A
Category
Medical Device
Distribution
Distributed nationwide