Oregon recalls
3,528 federal recalls affecting Oregon in the last 12 months - 196 Oregon-specific plus 3,332 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-04-01FDA-DeviceI.T.SClass IINationwideStop using I.T.S. GmbH olecranon plates before MRI
I.T.S. GmbH olecranon plates and olecranon hook plates used in orthopedic surgery may heat up more than expected during MRI scans under certain conditions. Updated safety testing found higher temperature increases than the original instructions stated.
- 2026-04-01FDA-DeviceI.T.SClass IINationwideContact your doctor about I.T.S. GmbH Pilonplate
I.T.S. GmbH has recalled certain Pilonplate devices used in orthopedic surgery because new MRI safety testing found they heat up more than expected during MRI scans under certain conditions. The devices affected include Anterolateral Tibia Plates, Pilon Plates 4mm, and Pilon Plates Small with specific article and lot numbers.
- 2026-04-01FDA-DeviceI.T.SClass IINationwideContact your surgeon about I.T.S. calcaneus plate
I.T.S. GmbH's FR.O.H. Calcaneus Repair System (anterolateral calcaneus plate, Article Number 21064-60) may heat more than expected during MRI scans under certain conditions. New testing found higher radiofrequency-induced temperature increases than the original instructions stated. Only 4 units were distributed nationwide.
- 2026-04-01FDA-DeviceI.T.SClass IINationwideCheck MRI safety if you have this shoulder plate
I.T.S. GmbH issued a recall for certain Humeral Head Plate with Angular Stability implants used in shoulder surgery. Testing found the device may heat up more than expected during MRI scans under certain conditions. The product labeling did not reflect these updated safety findings.
- 2026-04-01FDA-DeviceI.T.SClass IINationwideContact your surgeon about I.T.S. clavicle plate
I.T.S. GmbH clavicle plates used in shoulder surgery may heat up more than expected during MRI scans under certain conditions. New testing found higher temperature increases than the original instructions stated. This affects specific article numbers and lot numbers distributed across the US.
- 2026-04-01FDA-DeviceI.T.SClass IINationwideCheck MRI safety info for I.T.S. radius plates
I.T.S. GmbH's Radius Plate PROlock II (a surgical implant for wrist fractures) has been recalled because new MRI safety testing found the device heats up more than the instructions said it would under certain MRI scanner conditions. The original safety information in the product labeling did not reflect these higher temperature increases.
- 2026-04-01FDA-DeviceGEClass IINationwideStop using affected GE Imactis CT-Navigation systems
GE Medical Systems' Imactis CT-Navigation System (Models E85101LA and E85101LP) has a potential issue where the needle's simulated path shown to the doctor may not match where the needle actually goes during CT-guided procedures. This discrepancy could affect the accuracy of needle placement during medical procedures. No injuries have been reported.
- 2026-04-01FDA-DeviceNavajo ManufacturingClass INationwideStop using Handy Solutions heating pad model 25607
The Handy Solutions Neck & Shoulders Heating Pad (model 25607) can overheat and cause burns if folded while in use or placed under your body. When folded, the device's safety temperature sensor cannot detect the excessive heat, so it does not shut off. The pad may emit a burning smell before melting or catching fire.
- 2026-04-01FDA-DeviceMerit MedicalClass INationwideStop using Merit Medical BioFlo DuraMax Catheter
Merit Medical Systems is recalling certain BioFlo DuraMax Catheters because the sheath introducer may not split as designed. This defect could lead to complications during medical procedures, including bleeding, blood clots, or difficulty removing the catheter.
- 2026-04-01FDA-DeviceMerit MedicalClass INationwideStop using Merit Medical DuraMax catheters
Merit Medical Systems is recalling certain DuraMax chronic hemodialysis catheters due to a design defect in the 16F dual-valved splittable sheath introducer. The sheath may not split properly during insertion, which could cause bleeding, blood clots, catheter malfunction, or loss of future vascular access.
- 2026-04-01FDA-DeviceMerit MedicalClass INationwideStop using Merit Medical 16F sheath introducer
Merit Medical Systems is recalling specific lots of its 16F dual-valved splittable sheath introducer because of a design defect that may prevent it from splitting properly during use. This could lead to serious complications including bleeding, blood clots, or damage to blood vessels.
- 2026-04-01FDA-DeviceMerit MedicalClass INationwideStop using Merit Medical ProGuide dialysis catheters
Merit Medical Systems is recalling certain ProGuide Chronic Dialysis Catheters with a 16F dual-valved splittable sheath introducer due to a design defect. The sheath may not split as intended during insertion, which could cause serious complications including bleeding, blood clots, or damage to blood vessels.
- 2026-04-01FDA-DeviceMerit MedicalClass INationwideStop using Merit Medical CentrosFLO catheters
Merit Medical Systems is recalling certain CentrosFLO hemodialysis catheters because the introducer sheath may not split properly during placement. This design defect could lead to bleeding, blockages, or difficulty placing the catheter correctly.
- 2026-04-01FDA-DeviceErbeClass INationwideStop using Erbe USA Flexible Cryoprobe
Erbe USA Inc is recalling specific lots of Flexible Cryoprobe devices used in surgery because the probes may rupture or burst when activated. This defect could affect patient safety during the procedure. No injuries have been reported to date.
- 2026-04-01FDA-DeviceErbeClass INationwideStop using Erbe USA Flexible Cryoprobe devices
Erbe USA Inc. is recalling certain Flexible Cryoprobe surgical devices (model OD 1.7mm, L1.15mm, REF: 20402-410) because the probes may rupture or burst when activated during surgery. This defect could cause injury to patients or surgical staff. No injuries have been reported so far.
- 2026-04-01FDA-DeviceErbeClass INationwideStop using Erbe USA cryoprobes immediately
Erbe USA has recalled certain flexible cryoprobes used in surgery because they may rupture or burst when activated. The defect could cause unexpected device failure during a procedure. No injuries have been reported, but the risk requires immediate action.
- 2026-04-01FDA-FoodNuts.comClass INationwideStop eating Nuts.com Espresso Malted Milk Balls
Nuts.com Espresso Malted Milk Balls contain wheat and soy allergens that are not listed on the package label. The ingredient soy lecithin contains soy, and wheat is also present in the product. People with wheat or soy allergies could have a serious reaction if they eat this product.
- 2026-04-01FDA-FoodAlbertsonsClass IIStop using Lucerne 2% Cottage Cheese
Lucerne 2% Cottage Cheese (24 oz. tubs, UPC 0 21130 07662 8) may contain a small stainless steel spring. The spring could be present in the product and may pose a choking or injury risk if ingested or if broken pieces become sharp. No injuries have been reported.
- 2026-04-01FDA-FoodMangalmClass IIDo not eat Tops GOLD Green Chilli Pickle
Tops GOLD Green Chilli Pickle (31.74 oz cans) may contain higher-than-allowed levels of erucic acid from the mustard oil ingredient. Erucic acid in high amounts can pose health risks. The affected product was distributed in California, Nevada, Oregon, Utah, and Washington.
- 2026-04-01FDA-FoodMangalmClass IIStop using Tops GOLD Stuffed Red Chilli Pickle
Tops GOLD Stuffed Red Chilli Pickle (31.74 oz cans) may contain elevated levels of erucic acid from the mustard oil ingredient. Erucic acid in high amounts can pose health risks with prolonged consumption. The affected product was distributed in California, Nevada, Oregon, Utah, and Washington.
- 2026-04-01FDA-FoodMangalmClass IIStop using Tops GOLD Khatta Meetha Pickle
Tops GOLD Khatta Meetha Pickle (33.51 oz cans) may contain high levels of erucic acid, a harmful substance sometimes found in mustard oil. The affected product was distributed in California, Nevada, Oregon, Utah, and Washington. No injuries have been reported.
- 2026-04-01FDA-FoodMangalmClass IIDo not eat Tops GOLD Lime Pickle
Tops GOLD Lime Pickle (31.74 oz cans, made in India) may contain elevated levels of erucic acid from the mustard oil ingredient. Erucic acid in high amounts can pose health risks if consumed regularly. The recall affects 40 cases distributed in California, Nevada, Oregon, Utah, and Washington.
- 2026-04-01FDA-FoodMangalmClass IIStop using Tops GOLD Mango Pickle
Tops GOLD Mango Pickle made with mustard oil may contain elevated levels of erucic acid, a compound that can pose health risks if consumed regularly in high amounts. The recalled products were distributed in California, Nevada, Oregon, Utah, and Washington. No illnesses have been reported.
- 2026-04-01FDA-FoodMangalmClass IIDon't eat Tops GOLD Mixed Pickle
Tops GOLD Mixed Pickle may contain erucic acid from the mustard oil ingredient. Erucic acid can be harmful if consumed in high amounts over time. This recall affects two sizes sold in the Western U.S.
- 2026-04-01FDA-FoodRose and ShoreClass IIStop using Rose and Shore Margarita pizza
Rose and Shore frozen margarita thin crust pizza may contain metal pieces from contaminated tomatoes. The affected product was distributed to retailers in California, Oregon, Arizona, Idaho, and Texas. No injuries have been reported.
- 2026-04-01FDA-FoodPacific Coast FreshClass IIStop using King Harvest Spinach Hummus
King Harvest brand Spinach Hummus (10 oz tubs) may contain small aluminum pieces. The affected product was distributed in Oregon and Washington and has a best-by date of 2/27/2026. No injuries have been reported.
- 2026-04-01FDA-FoodPacific Coast FreshClass IIStop eating King Harvest Black Olive Hummus
King Harvest brand Black Olive Hummus (10 oz tubs, UPC 025726 311216) may contain small aluminum pieces. The affected products were distributed in Oregon and Washington with a best-by date of 3/2/2026. No injuries have been reported.
- 2026-04-01FDA-FoodPacific Coast FreshClass IIStop eating King Harvest Balsamic Hummus
King Harvest brand Balsamic Hummus (10 oz containers, best by 3/2/2026) may contain small aluminum pieces. The hummus was distributed in Oregon and Washington. No injuries have been reported.
- 2026-04-01FDA-FoodPacific Coast FreshClass IIStop eating King Harvest Sundried Tomato Hummus
King Harvest brand Sundried Tomato Hummus (10 oz containers, UPC 025726 311186) may contain small aluminum pieces. The affected product was distributed in Oregon and Washington with a best-by date of 3/2/2026. No injuries have been reported.
- 2026-04-01FDA-FoodPacific Coast FreshClass IIStop eating King Harvest Roasted Red Pepper Hummus
King Harvest brand Roasted Red Pepper Hummus may contain small aluminum pieces. The affected products are 10 oz and 17 oz tubs with a Best By date of 3/2/2026, distributed in Oregon and Washington. No injuries have been reported.
Get notified about new Oregon recalls
Free weekly digest. Add Oregon to your profile to filter alerts to your state.
Get the Sunday Brief