Product Recalls in Oregon
Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,457 recalls have been distributed to Oregon in the last 12 months.
Showing 29101–29120 of 50,914 recalls
Recalled Item: NON-STERILE SAMPLE Recalled by Sorin Group USA, Inc. Due to Medtronic...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NON-STERILE SAMPLE Recalled by Sorin Group USA, Inc. Due to Medtronic...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERILE SAMPLE SORIN GROUP Recalled by Sorin Group USA, Inc. Due to...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Obagi-C Rx System C-Therapy Night Cream Recalled by Valeant Pharmaceuticals...
The Issue: Labeling: Incorrect or Missing Package Insert - Obagi-C Rx System C-Therapy...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: parodontax WHITENING (Stannous fluoride) Daily Fluoride Anticavity and...
The Issue: Presence of Foreign Substance: possibility of the presence of metal in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kettle Brand Krinkle Cut Potato Chips Spicy Queso Recalled by Kettle Foods,...
The Issue: Carbohydrates on nutritional facts panel are stated as 3g/serving when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PB Crave Recalled by Peanut Butter holdings, LLC Due to Mislabeling
The Issue: Product mislabeled. "'Contains " allergen statement under the ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle Recalled...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Deluxe Bone Marrow Biopsy/Aspiration Tray Recalled by Robert Busse &...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laceration Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse Hospital...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...
The Issue: The sterile drape material may contain a pinhole compromising its integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System Recalled by...
The Issue: The sterile drape material may contain a pinhole compromising its integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.