State

Oregon product recalls

73,106 recalls have nationwide distribution and so reach Oregon. 7,529 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total: 7,529
Critical: 876
Severe: 1,805
Most recent: 2026-09-23

Of the 7,529 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 1,805 (24%) are Severe.

Which agencies issued them

These figures cover only the 7,529 recalls whose distribution notice names Oregon specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12501–12525 of 80635

HighCPSC·24189·2024-04-05
Procter & Gamble Recalls 8.2 Million Defective Laundry Detergent Packet Bags
Procter & Gamble is recalling about 8.2 million bags of Tide, Gain, Ace, and Ariel laundry detergent packets because the outer packaging can split open near the zipper, risking serious injury, ingestion, or skin or eye injuries—especially to children.
Product
Tide Pods, Gain Flings, Ace Pods and Ariel Pods liquid laundry detergent packets packaged in flexible film bags. This recall announcement applies only to bags distributed in the United States.
Category
Consumer Product
Distribution
Distributed nationwide
CriticalCPSC·24180·2024-04-04
C2 Crank Cocking Aids for Excalibur Crossbows Recalled for Impact Injury and Laceration Hazards
Excalibur Crossbow is recalling about 15,000 C2 Crank cocking aids because the plastic cocking hooks can break during use and become flying projectiles, causing impact injuries and lacerations. One consumer reportedly suffered a permanent eye injury.
Product
C2 Crank Cocking Aid for Crossbows
Category
Consumer Product
Distribution
Distributed nationwide
CriticalCPSC·24179·2024-04-04
Essential Medical Supply Reannounces Adult Bed Rails Recall; Entrapment and Asphyxia
Essential Medical Supply is reannouncing a recall of approximately 272,000 Endurance® Hand Bed Rails due to entrapment and asphyxiation hazards. Two additional deaths have been reported since the original 2021 recall.
Product
Endurance® Hand Bed Rails
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·24181·2024-04-04
BLACK+DECKER Garment Steamers Recalled Nationwide for Burn Hazard
Empower Brands is recalling approximately 1.6 million BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, causing burn injuries. Consumers should stop using the steamers immediately and contact the manufacturer for a full refund.
Product
BLACK+DECKER Model HGS011 Easy Garment Steamers
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·24V252000·2024-04-04
Terex Advance Recalls 2023 Commander Vehicles for Steering Defect
Terex Advance is recalling 2023 Commander vehicles because steering components may not be installed correctly, increasing the risk of a crash.
Product
TEREX ADVANCE — TEREX ADVANCE COMMANDER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24184·2024-04-04
Zazaba International Recalls Grão de Gente Baby Nests for Suffocation and Fall Hazards
Zazaba International is recalling about 430 Grão de Gente baby nests sold online from March 2023 through August 2023 due to suffocation risk and fall and entrapment hazards that violate federal infant sleep product safety standards.
Product
Grão de Gente Baby Nests
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24178·2024-04-04
Walmart Recalls Mainstays Electric Mini Choppers for Laceration Hazard
Walmart is recalling about 51,750 Mainstays Electric Mini Choppers because the blade can operate unexpectedly during assembly or when not enclosed, causing cuts. Five lacerations have been reported, two requiring medical attention.
Product
Mainstays Electric Mini Choppers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24185·2024-04-04
Zazaba International Recalls Grão de Gente Crib Bumper Bedding Sets for Suffocation Risk
Zazaba International is recalling about 795 Grão de Gente padded crib bumper bedding sets sold online between March and August 2023 due to suffocation hazard. Infants can suffocate if they roll into the bumper, which violates the federal Safe Sleep for Babies Act of 2021.
Product
Grão de Gente Crib Bumper Bedding Sets
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·24183·2024-04-04
Children's Two-Piece Pajamas and Lounge Dresses Flammability Violation Recall
Koala Tree Enterprises (DBA Lovey & Grink) is recalling approximately 23,720 children's two-piece pajamas and lounge dresses because they violate federal flammability regulations for children's sleepwear and pose a risk of burn injuries.
Product
Children's Two-Piece Pajamas and Lounge Dresses
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·24182·2024-04-04
Thule RideAlong Rear-Mounted Child Bike Seats Recalled for Chemical Hazard
Thule is recalling about 8,640 RideAlong rear-mounted child bike seats because the harness padding can contain DecaBDE, a flame retardant, in excess of regulatory limits. DecaBDE can be toxic if ingested or if it contacts skin or eyes.
Product
Thule RideAlong rear-mounted Child Bike Seats
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1326-2024·2024-04-03
Catheter Extension Recalled by Fresenius Due to Chemical Leachables
Fresenius is recalling 479,978 stay-safe Luer Lock Catheter Extensions due to chemical leachables in the tubing. Healthcare providers should contact the manufacturer for replacement information.
Product
stay-safe /Luer Lock Catheter Ext. 18 in
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1286-2024·2024-04-03
Nimbus II Infusion Pump Systems Recalled for Multiple Potential Device Failures
InfuTronix is recalling 52,328 Nimbus II Infusion Pump Systems due to potential failure modes including battery failure, system errors, drug product leakage, flow rate issues, and housing damage. The devices will no longer be available or supported after June 20, 2024.
Product
Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT1078; Nimbus II EpiD IT1124; Nimbus II EMS IT1063; Ambulatory Infusion Pump and components
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1323-2024·2024-04-03
Catheter Extension Tubing Recalled Due to Identified Leachable Substances
Fresenius Medical Care is recalling 114,982 stay-safe Safe Lock Catheter Extensions due to peroxide cross-linked tubing leachables. Patients and healthcare providers are advised to discontinue use and contact the manufacturer for replacement.
Product
stay-safe /Safe Lock Catheter Ext. 12 in
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V248000·2024-04-03
Aston Martin Recalls 2021 DBX Vehicles for Loose Driveline Fasteners
Aston Martin is recalling 2021 DBX vehicles because loose fasteners on the front propeller shaft and differential may cause loss of front wheel drive or engine stall.
Product
ASTON MARTIN — ASTON MARTIN DBX
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1327-2024·2024-04-03
FDA Recalls Fresenius Catheter Extension Tubing Due to Chemical Leachables
Fresenius Medical Care is recalling 105,700 stay-safe /Luer Catheter Extension 6 in devices nationwide due to chemical leachables identified in the peroxide cross-linked tubing. FDA classified this as a Class I recall.
Product
stay-safe /Luer Catheter Ext. 6 in
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1285-2024·2024-04-03
Nimbus Ambulatory Infusion Pump recalled due to multiple failure modes
InfuTronix is recalling Nimbus Infusion Pump Systems (Nimbus Flex, Nimbus PainPro) due to potential battery failure, system errors, drug leakage, flow rate abnormalities, and housing damage. About 52,328 units are affected nationwide.
Product
Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); Catalog Number IT1025. Ambulatory Infusion Pump and components
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0429-2024·2024-04-03
Treprostinil Injection recalled nationwide due to particulate matter contamination
Par Pharmaceutical is recalling Treprostinil Injection nationwide due to the presence of particulate matter. This FDA Class I recall affects 466 vials of lot 57014 distributed throughout the United States.
Product
Treprostinil Injection, 20 mg/20 mL (1 mg/mL), For Subcutaneous or Intravenous Infusion Only, 20 mL Multiple-Dose Vial, Rx Only, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977. NDC: 42023-206-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1324-2024·2024-04-03
FDA Recalls stay-safe Luer Lock Adapter for Chemical Leachables
The FDA is recalling approximately 828,954 stay-safe Luer Lock Adapters due to chemical leachables identified in the peroxide cross-linked tubing. The nationwide recall affects all lots of Model Number 050-95003.
Product
stay-safe /Luer Lock Adapter 4 in
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1325-2024·2024-04-03
Stay-safe Luer Lock catheter extension recalled for chemical leachables
Fresenius is recalling 663,221 stay-safe Luer Lock catheter extension units nationwide due to chemical leachables (NDL PCBAs) identified in the tubing.
Product
stay-safe /Luer Lock Catheter Ext. 12 in
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1383-2024·2024-04-03
RELAY PRO Thoracic Stent-Graft System recalled for incorrect size
Bolton Medical Inc. is recalling 21 RELAY PRO Thoracic Stent-Graft Systems because the stent-graft inside the delivery system is the incorrect size.
Product
RELAY PRO Thoracic Stent-Graft System, containing one endovascular stent-graft system, IFU, and patient tracking card, sterile: (a) Part number 28-M4-34-100-34U; (b) Part number 28-M4-30-095-30U; (c) Part number 28-M4-46-155-46U; (d) Part number 28-M4-32-155-32S; (e) Part…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1388-2024·2024-04-03
Epix Universal Clip Applier Recalled for Potential Clip Loading Failure
Applied Medical Resources is recalling the Epix Universal Clip Applier because the device may fail to load the surgical clip after the trigger is actuated. Units were distributed worldwide.
Product
Epix Universal Clip Applier, REF: CA500, STERILEEO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0408-2024·2024-04-03
HYDROmorphone Injectable Recalled Due to Sterility Assurance Failure
SCA Pharmaceuticals is recalling HYDROmorphone HCl injections due to lack of assurance of sterility. Patients who received the affected lot should contact their healthcare provider.
Product
HYDROmorphone HCl 25 mg/25 mL in 0.9% Sodium Chloride Injection, (Concentration = 1mg/mL), 25 mL fill 30 mL Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0303-17, Bar Code 7004030317
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1358-2024·2024-04-03
Bio-Rad QXDx BCR-ABL diagnostic kit recalled for calibration errors
Bio-Rad Laboratories is recalling a diagnostic test kit due to incorrect calibrations and controls that may produce inaccurate test results. Patients and healthcare providers should contact the manufacturer.
Product
Bio-Rad, REF: 12005660, QXDx BCR-ABL %IS Kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1395-2024·2024-04-03
Emergency traction splint adhesive failure may compromise device function
Emergency Products & Research is recalling 190,000 O.T.D. traction splints because adhesive may fail to secure the pole insert, potentially compromising function in emergency medical situations.
Product
O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0414-2024·2024-04-03
Phenylephrine HCl Injections Recalled Nationwide for Sterility Assurance Issues
SCA Pharmaceuticals is recalling Phenylephrine HCl injections nationwide affecting approximately 33,000 units due to lack of assurance of sterility.
Product
PHENYLephrine HCl 1000 mcg/10 mL in 0.9% Sodium Chloride Injection, (Concentration = 100 mcg/mL), 10 mL fill 12 mL Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0810-12, Bar Code 70004081012
Category
Drug
Distribution
Distributed nationwide