State

Oregon product recalls

73,566 recalls have nationwide distribution and so reach Oregon. 7,533 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total: 7,533
Critical: 876
Severe: 2,128
Most recent: 2026-10-14

Of the 7,533 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 2,128 (28%) are Severe.

Which agencies issued them

These figures cover only the 7,533 recalls whose distribution notice names Oregon specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26576–26600 of 81099

HighFDA (Devices)·Z-1831-2021·2021-06-16
Laboratory Software Device May Produce Erroneous Results from Inadequate Instructions
Normand Remisol Advance Data Manager versions 1.5–1.9 have insufficient instructions for proper rule programming and testing. User-written rules may not be properly validated, potentially leading to erroneous laboratory results.
Product
Normand Remisol Advance Data Manager is a software device that interfaces between laboratory information systems (LIS) and laboratory instruments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1802-2021·2021-06-16
Alphatec Insignia Anterior Cervical Plate Screw Blocking Mechanism Disassociation Recall
Alphatec Spine is recalling the Insignia Anterior Cervical Plate System due to a potential failure in the screw blocking mechanism that may disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0119, Insignia, ACP, 1-Level, 19 mm, Rx Only, Non-Sterile, UDI: (01)00190376268453
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1812-2021·2021-06-16
Anterior Cervical Plate System Screw Mechanism May Fail Intraoperatively
Alphatec Spine is recalling the Atec Insignia Anterior Cervical Plate System due to a potential defect in the screw blocking mechanism that could disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0242 Insignia, ACP, 2-Level, 42 mm, Rx Only, Non-Sterile, UDI: (01)00190376268415
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1844-2021·2021-06-16
Quanta System Sterile Optical Laser Fiber Recall for Potential Sterility Compromise
Quanta System is recalling 307 reusable sterile optical laser fibers nationwide due to potential sterility compromise. The affected devices were distributed through six U.S. distributors.
Product
Quanta System Sterile Optical Laser Fiber, reusable
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21151·2021-06-16
Cove Appliance 24-inch Built-in Dishwashers Recalled for Fire Hazard
Cove Appliance is recalling about 42,000 built-in dishwashers because the heating element can fail to shut off and overheat, creating a fire hazard. The company has received five reports of burning smells, flames, and smoking inside the dishwashers, though no injuries have been reported.
Product
Cove Appliance 24-inch built-in dishwashers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1804-2021·2021-06-16
Atec Insignia Anterior Cervical Plate System Recall: Potential Screw Mechanism Failure
Alphatec Spine is recalling 7 units of the Atec Insignia Anterior Cervical Plate System because the screw blocking mechanism could disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0121, Insignia, ACP, 1-Level, 21 mm, Rx Only, Non-Sterile, UDI: (01)00190376268477
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1813-2021·2021-06-16
Atec Insignia Anterior Cervical Plate System recall due to potential screw mechanism failure
Alphatec Spine is recalling Atec Insignia Anterior Cervical Plate System units due to a potential defect where the screw blocking mechanism may disassociate or unlock during or after surgery. No adverse events have been reported.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0244 Insignia, ACP, 2-Level, 44 mm, Rx Only, Non-Sterile, UDI: (01)00190376268507
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1838-2021·2021-06-16
Medical Device Software Defects in RayStation Treatment Planning System
RayStation radiation therapy treatment planning software versions 6 through 10A contain defects that may cause misleading dose evaluations and contouring errors. Healthcare facilities should verify treatment plans and contact the manufacturer for guidance.
Product
RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 , 8.0.0.6 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 , 9.2.0.483 , 10.0.0.1154 , 10.0.1.52 or 10.1.0.613 .
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1820-2021·2021-06-16
Atec Insignia Anterior Cervical Plate System Screw Mechanism Recall
Alphatec Spine is recalling the Atec Insignia Anterior Cervical Plate System due to potential disassociation or postoperative unlock of the screw blocking mechanism during or after cervical spine surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0358 Insignia, ACP, 3-Level, 58 mm, Rx Only, Non-Sterile, UDI: (01)00190376268606
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1801-2021·2021-06-16
Anterior cervical plate system screw mechanism may disassociate during or after surgery
Alphatec Spine's Atec Insignia Anterior Cervical Plate System has a potential defect where the screw blocking mechanism may disassociate during or after surgery, which could compromise spinal stabilization.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0118, Insignia, ACP, 1-Level, 18 mm, Rx Only, Non-Sterile, UDI: (01)00190376268446
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0663-2021·2021-06-16
Adobo para Chorizo Seasoning Recalled for Undeclared Soy Lecithin
Jesmar Spices, LLC is recalling Adobo para Chorizo Seasoning for Sausage because it contains undeclared soy lecithin from chocolate used in the product. The allergen is not listed on the product label.
Product
Adobo para Chorizo - Chorizo Marinade - Seasoning for Sausage. Product is packaged in a plastic bucket seal with lid, 5 gallons. No UPC. The label is read in parts: "*** Adobo para Chorizo *** Seasoning for Sausage *** Ingredients: Dried Chilies, vinegar, almonds, salt…
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-1803-2021·2021-06-16
Cervical Spine Plate System Screw Mechanism May Disassociate or Unlock
Alphatec Spine recalls its Atec Insignia Anterior Cervical Plate System due to a potential defect in the screw blocking mechanism, which may disassociate or unlock during or after spinal surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0120, Insignia, ACP, 1-Level, 20 mm, Rx Only, Non-Sterile, UDI: (01)00190376268460
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1824-2021·2021-06-16
Alphatec Insignia Cervical Plate System: Screw Mechanism Disassociation Risk
Alphatec recalls the Insignia Anterior Cervical Plate System due to risk that the screw blocking mechanism may disassociate during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0468 Insignia, ACP, 4-Level, 68 mm, Rx Only, Non-Sterile, UDI: (01)00190376268675
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1822-2021·2021-06-16
Anterior Cervical Plate System Screw Mechanism Recall
Alphatec Spine recalls Atec Insignia Anterior Cervical Plate Systems because the screw blocking mechanism may fail during or after surgery. The mechanism may disassociate or unlock, potentially compromising implant stability.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0362 Insignia, ACP, 3-Level, 62 mm, Rx Only, Non-Sterile, UDI: (01)00190376268620
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1842-2021·2021-06-16
FDA Recalls Olympus Sterile Optical Laser Fibers for Potential Sterility Compromise
Quanta System is recalling Olympus Sterile Optical Laser Fibers nationwide due to potentially compromised sterility. Approximately 26,925 units distributed through six U.S. distributors are affected.
Product
Olympus Sterile Optical Laser Fiber, single use and reusable
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1815-2021·2021-06-16
Anterior Cervical Plate System Recalled for Potential Screw Mechanism Failure
Alphatec Spine is recalling the Atec Insignia Anterior Cervical Plate System because the screw blocking mechanism could disassociate or unlock during or after cervical spine surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0250 Insignia, ACP, 2-Level, 50 mm, Rx Only, Non-Sterile, UDI: (01)00190376268538
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1846-2021·2021-06-16
Radiotherapy positioning software may delay patient movement display
Brainlab's ExacTrac Dynamic radiotherapy positioning software may delay display of patient movement during high-dose treatments, risking treatment precision errors. 22 systems affected across 11 U.S. states.
Product
ExacTrac Dynamic software, Model 20910-01B ETD Positioning and Monitoring Installer 1.0.2 - Product Usage: intended to position patients at an accurately defined point within the treatment beam of a medical accelerator for stereotactic radiosurgery or radiotherapy procedures, to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1814-2021·2021-06-16
Anterior Cervical Plate System Screw Mechanism May Disassociate or Unlock
Alphatec Spine recalls its Insignia Anterior Cervical Plate System because the screw blocking mechanism may disassociate during spinal surgery or unlock afterward. Healthcare providers should contact the manufacturer for guidance.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0248 Insignia, ACP, 2-Level, 48 mm, Rx Only, Non-Sterile, UDI: (01)00190376268521
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1827-2021·2021-06-16
Anterior cervical plate system screw blocking mechanism defect recalled
Alphatec Spine's Atec Insignia anterior cervical plate system has a defect in the screw blocking mechanism that could disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0482 Insignia, ACP, 4-Level, 82 mm, Rx Only, Non-Sterile, UDI: (01)00190376268712
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1809-2021·2021-06-16
Anterior cervical plate system screw blocking mechanism may disassociate
Alphatec Spine Inc. is recalling the Atec Insignia anterior cervical plate system because the screw blocking mechanism may disassociate intraoperatively or unlock postoperatively. No injuries reported.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0236 Insignia, ACP, 2-Level, 36 mm, Rx Only, Non-Sterile, UDI: (01)00190376268385
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1823-2021·2021-06-16
Anterior cervical plate system screw mechanism may disassociate or unlock
The Alphatec Insignia anterior cervical plate system may have a defect where the screw blocking mechanism disassociates during surgery or unlocks afterward. Consult your doctor if you have this implant.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0364 Insignia, ACP, 3-Level, 64 mm, Rx Only, Non-Sterile, UDI: (01)00190376268637
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1811-2021·2021-06-16
Alphatec Insignia Anterior Cervical Plate System screw locking mechanism failure
Alphatec Spine is recalling the Insignia Anterior Cervical Plate System due to a potential failure in the screw locking mechanism. The mechanism may disassociate or unlock during or after spinal surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0240 Insignia, ACP, 2-Level, 40 mm, Rx Only, Non-Sterile, UDI: (01)00190376268408
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1817-2021·2021-06-16
Atec Insignia Anterior Cervical Plate System Screw Blocking Mechanism Risk
The FDA is recalling certain Atec Insignia Anterior Cervical Plate Systems due to a potential defect in the screw blocking mechanism that could disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0352 Insignia, ACP, 3-Level, 52 mm, Rx Only, Non-Sterile, UDI: (01)00190376268576
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1821-2021·2021-06-16
Anterior Cervical Plate System Screw Blocking Mechanism May Disassociate
Alphatec Spine is recalling the Atec Insignia Anterior Cervical Plate System due to a potential defect in the screw blocking mechanism. The screws may disassociate or unlock during or after surgery, risking implant failure.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0360 Insignia, ACP, 3-Level, 60 mm, Rx Only, Non-Sterile, UDI: (01)00190376268613
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1845-2021·2021-06-16
DePuy Synthes Hip Prosthesis Recall Due to Incorrect Size Labeling
DePuy Orthopaedics recalled 50 hip prostheses with incorrect part numbers and sizes etched on the devices. The affected Lot D20111130 was distributed domestically and to Bermuda.
Product
DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer semi-constrained cemented prosthesis. Part Number: 1365-21-000, Part Description: ARTICUL/EZE BALL 32 +1 GR
Category
Medical Device
Distribution
21 states