State

Oregon product recalls

72,971 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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6951–6975 of 80497

SevereFDA (Devices)·Z-1630-2025·2025-05-07
GE Healthcare Anesthesia Systems Recalled Over Ventilation Failure
GE Healthcare is recalling certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems because they may not provide effective ventilation in Volume Control Ventilation (VCV) mode. The issue does not affect Pressure Control Ventilation (PCV), PCV-VG, or manual ventilation modes.
Product
GE Healthcare Carestation 650 SE, Model/REF Number 1012-9650-012. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1625-2025·2025-05-07
GE Healthcare CARESTATION 620 A2 Anesthesia System Ventilation Failure
Certain GE Healthcare CARESTATION anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation (VCV) mode. Alternative ventilation modes or manual ventilation can be used.
Product
GE Healthcare CARESTATION 620 A2, Model/REF Number 1012-9620-002. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1635-2025·2025-05-07
GE Healthcare CARESTATION 750 Anesthesia System Volume Control Ventilation Failure
Certain GE Healthcare CARESTATION 750 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Affected systems can deliver ventilation through alternative modes or manual ventilation.
Product
GE Healthcare CARESTATION 750 A1, Model/REF Number 1012-9750-000. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1704-2025·2025-05-07
Enhanced Verify Evaluation Handset May Fail to Connect to Neurostimulator
Medtronic Enhanced Verify Evaluation Handsets (CFN HH90130FA) may fail to communicate with neurostimulators due to faster processing speed, causing therapy to stop and patients to experience return of underlying symptoms.
Product
Enhanced Verify Evaluation Handset (CFN HH90130FA)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1696-2025·2025-05-07
Quantum Informatics VISION LIVE VUE Patient Monitor Recalled Without FDA Clearance
Spectrum Medical Ltd. is recalling the Quantum Informatics VISION / LIVE VUE patient monitoring software because it was marketed without required FDA clearance or approval.
Product
Brand Name: Quantum Informatics - VISION / LIVE VUE Product Name: Monitor, Physiological, Patient (Without Arrhythmia Detection or Alarms) Product Description: VISION / LIVE VUE is a software-only device (SaMD) that is intended to provide near real-time patient safety and clini
Category
Medical Device
Distribution
38 states
SevereFDA (Devices)·Z-1695-2025·2025-05-07
Quantum Informatics VIPER Physiological Monitor Recalled for Lack of FDA Clearance
Spectrum Medical Ltd. is recalling the Quantum Informatics VIPER, a patient monitoring software device, because it was marketed without required FDA clearance. The software is used in operating rooms to provide patient safety information.
Product
Brand Name: Quantum Informatics - VIPER Product Name: Monitor, Physiological, Patient (Without Arrhythmia Detection or Alarms) Product Description: VIPER is a software-only device (SaMD) that is intended to provide near real-time patient safety and clinical best practice soluti
Category
Medical Device
Distribution
38 states
SevereFDA (Devices)·Z-1626-2025·2025-05-07
GE Healthcare Carestation 620 SE Anesthesia System Ventilation Defect Recall
GE Healthcare is recalling certain Carestation 620 SE anesthesia systems (27 units) because they may not provide effective ventilation in Volume Control Ventilation mode. Alternative ventilation modes remain functional.
Product
GE Healthcare Carestation 620 SE, Model/REF Number 1012-9620-012. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1631-2025·2025-05-07
GE Healthcare Carestation Anesthesia Systems Ventilation Defect Recall
Certain GE Healthcare Carestation anesthesia delivery systems may fail to provide effective ventilation in Volume Control Ventilation (VCV) mode. Affected systems can still be used safely in Pressure Control Ventilation or Manual ventilation modes.
Product
GE Healthcare Carestation 650 A1, Model/REF Number 1012-9650-200. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1637-2025·2025-05-07
GE Healthcare CARESTATION 750c A1 Anesthesia System Ventilation Defect
GE Healthcare CARESTATION 750c A1 anesthesia systems may not provide effective ventilation in Volume Control Ventilation mode. Affected units can achieve ventilation through alternative modes or manual operation.
Product
GE Healthcare CARESTATION 750c A1, Model/REF Number 1012-9755-000. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1632-2025·2025-05-07
GE Healthcare CARESTATION 650C A1 Anesthesia System Ventilation Recall
GE Healthcare CARESTATION 650C A1 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Ventilation can be achieved using alternate modes or manual ventilation.
Product
GE Healthcare CARESTATION 650C A1, Model/REF Number 1012-9655-000. Anesthesia system.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1624-2025·2025-05-07
GE Healthcare CARESTATION anesthesia systems ventilation malfunction recall
GE Healthcare CARESTATION 620 A1 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Effective ventilation is available in Pressure Control or Manual ventilation modes.
Product
GE Healthcare CARESTATION 620 A1, Model/REF Number 1012-9620-000. anesthesia systems
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1699-2025·2025-05-07
Distal Femoral Augment medical device recall for defective screw
Waldemar Link GmbH & Co. KG is recalling Distal Femoral Augment devices because the preassembled femoral augment screw was missing its thread. The defect may affect proper device function.
Product
Distal Femoral Augment; Item Numbers: (1) 880-300/11 (Sz. 0 - cemented sm), (2) 880-300/21 (Sz. 0 - cemented lg), (3) 880-301/11 (Sz. 1-2 - cemented sm), (4) 880-301/21 (Sz. 1-2 - cemented lg), (5) 880-303/11 (Sz. 3-4 - cemented sm), (6) 880-303/12 (Sz. 3-4 - cemented md), (7) 88
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1702-2025·2025-05-07
Tibial Augment devices recalled for missing screw thread
Waldemar Link GmbH & Co. KG is recalling Tibial Augment devices distributed nationwide because preassembled Femoral Augment screws were delivered missing their threads.
Product
Tibial Augment; Item Numbers: (1) 880-331/11 (Sz. 1-2 - cemented x-sm), (2) 880-331/12 (Sz. 1-2 - cemented sm), (3) 880-331/13 (Sz. 1-2 - cemented md), (4) 880-331/21 (Sz. 1-2 - cemented lg), (5) 880-331/22 (Sz. 1-2 - cemented x-lg), (6) 880-331/23 (Sz. 1-2 - cemented xx-lg), (7)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0758-2025·2025-05-07
La Victoria Cilantro Salsa recalled for wood pieces in ingredient
La Victoria Cilantro Salsa (15.5 oz) is being recalled because the fresh cilantro ingredient may contain wood pieces. The product was distributed to California, Nevada, Oregon, Washington, and Michigan.
Product
La Victoria Cilantro Salsa; Med; Net Wt 15.5 OZ; UPC# 0 72101 34470 3; Distributed by: Megamex Foods, LLC Orange, CA 92868
Category
Food
Distribution
5 states
HighNHTSA·25V295000·2025-05-07
2025 Freightliner trucks recalled for insufficient air tank capacity
Daimler Trucks North America is recalling certain 2025 Freightliner, Western Star, and related models due to undersized air tanks that reduce braking performance and increase crash risk.
Product
FREIGHTLINER — FREIGHTLINER, WESTERN STAR 114SD, CASCADIA, BUSINESS CLASS M2, 49X
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V296000·2025-05-07
2025 Utilimaster Aeromaster Recalled for Missing Rear Seat Belts
Shyft Group is recalling 2025 Utilimaster Aeromaster vehicles because rear seat belts may be missing, increasing injury risk.
Product
UTILIMASTER — UTILIMASTER AEROMASTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V294000·2025-05-07
2022–2024 Audi Q5 Engine Cylinder Head Cover Screws Fire Risk
Volkswagen Group of America (Audi) is recalling certain 2022–2024 Q5 and Q5 Sportback Quattro vehicles due to cylinder head cover screws that may loosen, causing oil leaks and increasing fire risk. Dealers will inspect and replace the screws at no charge.
Product
AUDI — AUDI Q5 SPORTBACK, Q5
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1684-2025·2025-05-07
epoc BGEM BUN Test Cards for Blood Analysis System Recalled
Siemens Healthcare Diagnostics is recalling epoc BGEM BUN Test Cards (25 pk) due to discrepant high pH results when samples are introduced with higher injection volumes on affected sensor configurations.
Product
epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736515; epoc Software Version & Sensor Configuration: epoc Host SW v3.41.2, epoc NXS SW v4.14.9 & 4.14.11, Sensor Configuration 45.n.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1672-2025·2025-05-07
Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer Recall
Beckman Coulter is recalling certain DxC 500 AU Clinical Chemistry Analyzers due to incorrect sample barcode identification and processing errors that can result in erroneous and delayed test results.
Product
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 Software versions: V1.3, V1.4, V1.4.1, V1.4.2, V1.4.3 The Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer is an automated chemistry analyzer that meas
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1678-2025·2025-05-07
Belmont 3.0 Liter Disposable Set Recalled for Cracked Female Connector
Belmont Instrument LLC is recalling the 3.0 Liter Disposable Set (Model 903-00032) due to a potential crack in the female connector on the Heat Exchanger/patient line set that can cause fluid leaks during device priming.
Product
3.0 Liter Disposable Set (4 sets/case). Model Number: 903-00032. The P/N 903-00032 consists of 4 Large Volume Reservoirs (P/N 903-00018) and 4 Heat Exchanger/Patient Line set (P/N 403-00382). The two components are packaged separately in individual pouches and placed in the
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1714-2025·2025-05-07
Medline Sterile Water and Saline Bottles Leaking at Seal Interface
Medline is recalling sterile water and 0.9% normal saline bottles due to leaking at the peel-foil and bottle opening interface. The defect affects 159 units distributed nationwide and internationally.
Product
Medline procedure kits, labeled as: HAND, REF DYNJ902002J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0396-2025·2025-05-07
Levothyroxine Sodium Tablets 88 mcg Recall for Subpotency
Accord Healthcare is recalling Levothyroxine Sodium Tablets 88 mcg (Lot D2300044, expiring 12/2025) nationwide because the tablets are subpotent—below the required strength. Patients on this medication should contact their pharmacy or prescriber.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·25V293000·2025-05-07
2025 Polestar 3 vehicles recalled for faulty rearview camera display
Polestar is recalling certain 2025 Polestar 3 vehicles because the rearview camera image may not display when the vehicle is in reverse, reducing driver visibility and increasing crash risk.
Product
POLESTAR — POLESTAR POLESTAR 3
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1711-2025·2025-05-07
Medline Wound Care and Laceration Procedure Kits Recalled for Leaking Bottles
Medline is recalling Sterile Water and Sterile 0.9% Normal Saline bottles in wound care and laceration procedure kits due to leaking at the peel-foil and bottle opening interface.
Product
Medline procedure kits, labeled as: 1) WOUND CARE TRAY, REF DYNDA1412A; 2) LACERATION TRAY, REF DYNDL1263A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1675-2025·2025-05-07
Belmont Straight Inflow/Outflow Patient Line Kit recalled for potential connector crack
Belmont Instrument LLC is recalling the Straight Inflow/Outflow Patient Line Kit (Model 902-00037) due to a potential crack in the female connector on the Heat Exchanger set that may cause fluid leaks during use.
Product
Straight Inflow/Outflow Patient Line Kit. Model Number: 902-00037. Sterile, single-use, disposable set used with the Hyperthermia Pump. The Straight Inflow/Outflow Patient Line Kit (P/N 902-00037) consists of 4.4 Liter Reservoir (P/N 902-00034P), Heat Exchanger set (P/N 902
Category
Medical Device
Distribution
Distributed nationwide