State

Oregon product recalls

72,986 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 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8076–8100 of 80512

HighFDA (Devices)·Z-1072-2025·2025-02-12
VNS Therapy Generators May Stop Delivering Stimulation Due to Component Failure
The SenTiva and SenTiva Duo vagus nerve stimulation generators may stop delivering therapy due to an internal mechanical component becoming stuck, causing potential loss of seizure and depression control.
Product
SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D; Generators Part of the VNS Therapy System. Used for Vagus Nerve Stimulation (VNS).
Category
Medical Device
Distribution
41 states
HighFDA (Food)·F-0522-2025·2025-02-12
French Cruller Recall Due to Listeria Contamination Risk
FGF, LLC is recalling French Crullers (item 8201921) distributed nationwide in the US and Canada due to potential Listeria monocytogenes contamination.
Product
item 8201921 FRENCH CRULLER PFD 72x1.6 OZ, NET WT 6.48 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0492-2025·2025-02-12
FGF Frozen Bismark Donuts Recalled Due to Listeria Contamination Risk
FGF, LLC is recalling frozen Bismark donuts due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
Product
item 8201843 GEN BISMARK DONUT DGH FRZ 144x2OZ, NET WT 16.20 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0218-2025·2025-02-12
Prescription injection recalled for failed stability test results
Teva Pharmaceuticals is recalling Granix injection due to failed stability test results showing one peptide did not meet specification limits.
Product
GRANIX — GRANIX (TBO-FILGRASTIM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0525-2025·2025-02-12
Donuts Recalled for Potential Listeria Monocytogenes Contamination
FGF LLC is recalling egg-shaped donuts nationwide due to potential Listeria monocytogenes contamination. Approximately 2,017,614 cases were distributed in the US and Canada.
Product
item 8201926 FBALL/EGG SHPD DONUT PFD 78 X 2OZ, NET WT 8.78 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1084-2025·2025-02-12
Philips Allura and Azurion Patient Tables Recall Due to Finger Entrapment Risk
Philips is recalling AD7 and AD7X patient tables used in Allura and Azurion medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel are at risk of finger injury.
Product
AlluraXperFD20/10 System Code: (1) 722029
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0470-2025·2025-02-12
Cake Donut Rings Recalled for Potential Listeria Contamination
FGF, LLC is recalling cake donut rings due to potential contamination with Listeria monocytogenes. Distribution included nationwide US and Canada.
Product
item 8201779 GEN PLN CAKE DONUT RINGS PFD 90x2.5 OZ, NET WT 12.66LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0472-2025·2025-02-12
FGF Yeast Ring Donuts Recalled for Potential Listeria Contamination
FGF, LLC is recalling 2,017,614 cases of yeast ring donuts nationwide due to potential Listeria monocytogenes contamination. The affected product was produced on or before December 13, 2024.
Product
item 8201804 Yeast Ring Donut 108x2.15OZ, NET WT 13.06 LB
Category
Food
Distribution
Distributed nationwide
HighNHTSA·25V078000·2025-02-12
Porsche Recalls 2023 911 Models Due to Rear Seat Belt Bolt Issue
Porsche is recalling 2023 911 vehicles because rear seat belt buckle bolts may not be tightened properly, which could reduce occupant restraint during a crash.
Product
PORSCHE — PORSCHE 911
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0497-2025·2025-02-12
Just Baked Yeast Shells recalled for potential Listeria contamination
FGF, LLC is recalling Just Baked Yeast Shells due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.
Product
item 8201858 JUST BAKED YEAST SHELLS 120x1.88 OZ, NET WT 14.10 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1114-2025·2025-02-12
Endodontic Files Recalled for Excess Irradiation Causing Package Integrity Issues
US Endodontics is recalling endodontic files due to irradiation above specification, which may compromise package integrity. The recall affects 789,729 devices distributed in the US and internationally.
Product
Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK AP120253PK AP120313PK AP125213PK AP125253PK AP125313PK AP135213PK AP135253PK AP135313PK AP145213PK AP145253PK AP145313PK AP1GP213PK AP1GP253PK AP1GP313PK O.U.S. Products: EdgeFile X7 REF
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1089-2025·2025-02-12
Philips Azurion 5 M12 imaging system: finger entrapment risk during tabletop repositioning
Philips Azurion 5 M12 patient imaging systems pose a finger entrapment hazard during manual tabletop repositioning. Operators and service personnel risk finger injury from the longitudinal guiding rails.
Product
Azurion 5 M12 System Code: (1) 722227 (2) 722231
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1094-2025·2025-02-12
Philips Azurion and Allura Patient Table Finger Entrapment Risk
Philips Azurion 7 M20 and Allura patient tables pose a finger entrapment risk during manual repositioning. Fingers can get caught between the tabletop and guiding rails, potentially causing finger injury to operators and service personnel.
Product
Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) 722234 (4) 722282 System Code: (1) 722078 (2) 722223 (3) 722233
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0516-2025·2025-02-12
Apple Cider Cake Rings Recalled for Potential Listeria Contamination
FGF, LLC is recalling Just Baked Apple Cider Cake Rings due to potential Listeria monocytogenes contamination. Approximately 2,017,614 cases were distributed nationwide in the US and Canada.
Product
item 8201901 JUST BAKED APPLE CIDER CAKE RINGS WITH NATURAL FLAVORS 144x2.5OZ, NET WT 22.5 LB
Category
Food
Distribution
Distributed nationwide
HighNHTSA·25V079000·2025-02-12
Porsche Recalls 2025 911 Models Due to Headlight Glare Software Error
Porsche is recalling 878 2025 911 vehicles because a software error causes low beam headlights to create excessive glare for oncoming traffic, increasing crash risk.
Product
PORSCHE — PORSCHE 911
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V080000·2025-02-12
Audi Q5 and A7 high voltage batteries may overheat
Volkswagen is recalling certain 2021-2024 Audi Q5 and 2022 A7 e plug-in hybrid vehicles because the high-voltage battery may overheat, increasing the risk of a fire.
Product
AUDI — AUDI Q5, A7 E
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1045-2025·2025-02-12
GE Discovery XR656 HD X-ray system AEC control malfunctions during imaging
GE Medical Systems is recalling the Discovery XR656 HD X-ray imaging system due to a malfunction in the Automatic Exposure Control (AEC) feature. The defect allows continued X-ray exposure beyond intended limits without requiring operator acknowledgment.
Product
Discovery XR656 HD. X-Ray imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1097-2025·2025-02-12
PERMA-HAND Silk Sutures Recalled for Packaging Sterility Breach
Ethicon is recalling PERMA-HAND Silk Sutures that may have open seals on packaging due to manufacturing defects, risking sterility compromise and patient infection. Approximately 78,792 units were distributed nationwide and internationally.
Product
PERMA-HAND Silk Suture, REF: K872H, W723H, 623H, K833H; Perma-hand Silk Suture is indicated for use in general soft tissue approximation and/or ligation, including use in cardiovascular, ophthalmic and neurosurgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1098-2025·2025-02-12
Surgical sutures recalled for potential sterility breach
Ethicon is recalling ETHIBOND EXCEL Polyester Sutures due to open packaging seals that could compromise sterility and allow pathogen contamination. No illnesses have been reported.
Product
ETHIBOND EXCEL Polyester Suture, REF: 6664H, X425H, X872H, EH7491H. Not sold in US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0504-2025·2025-02-12
Just Baked Pumpkin Cake Munchkins recalled for potential Listeria contamination
FGF, LLC is recalling Just Baked Pumpkin Cake Munchkins nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume this product.
Product
item 8201867 JUST BAKED PUMPKIN CAKE MUNCHKINS 440x0.47 OZ, NET WT 12.93 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0512-2025·2025-02-12
FGF LLC Recalls Unfilled Bismarck Donuts for Listeria Contamination Risk
FGF LLC is recalling 2,017,614 cases of unfilled Bismarck donuts nationwide due to potential listeria monocytogenes contamination. Consumers should not consume the affected product.
Product
item 8201883 UNFLD BISMARK DONUT PFD 57x2.75OZ, NET WT 8.82 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0498-2025·2025-02-12
FGF LLC Just Baked Cake Rings Recalled for Potential Listeria Contamination
FGF, LLC recalls approximately 2,017,614 cases of Just Baked Cake Rings distributed nationwide due to potential contamination with Listeria monocytogenes.
Product
item 8201859 JUST BAKED CAKE RING 144x2.45 OZ, NET WT 22.05 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1079-2025·2025-02-12
Philips Allura patient tables recall due to finger entrapment risk
Philips recalls AD7 and AD7X patient tables in Allura and Azurion systems due to finger entrapment risk during manual repositioning. Operators and service personnel could suffer finger injuries.
Product
Allura Xper FD10C System Code: (1) 722001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0501-2025·2025-02-12
FGF LLC Recalls Just Baked Coffee Rolls Over Listeria Contamination Risk
FGF LLC is recalling 2,017,614 cases of Just Baked Coffee Rolls (78 x 3oz packages) due to potential Listeria monocytogenes contamination. The affected product was produced on or before 12/13/24 and distributed nationwide in the US and Canada.
Product
item 8201864 JUST BAKED COFFEE ROLLS 78x3OZ, NET WT 14.62 LB
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1078-2025·2025-02-12
Philips AlluraXper Patient Tables Pose Finger Entrapment Risk
Philips is recalling AD7 and AD7X patient tables used in Allura and Azurion fluoroscopy systems. Manual repositioning can trap fingers between the tabletop and rails, risking injury to operators and service personnel.
Product
AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027
Category
Medical Device
Distribution
Distributed nationwide