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. 2,590 recalls have been distributed to Oregon in the last 12 months.
Showing 14381–14400 of 50,914 recalls
Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns XX-large SKU: 9070 Recalled...
The Issue: Potential for open packaging seals compromising the sterility of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartGown Breathable Surgical Gowns with raglan sleeves X-large Recalled by...
The Issue: Potential for open packaging seals compromising the sterility of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns X-large SKU: 9040 Recalled by...
The Issue: Potential for open packaging seals compromising the sterility of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RoyalSilk Non-Reinforced Surgical Gowns XXX-large Recalled by Cardinal...
The Issue: Potential for open packaging seals compromising the sterility of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Steripath Gen2 Blood Collection System Model Number/Description...
The Issue: Due to an uptick of complaints associated with premature needle retraction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetaminophen Oral Suspension Recalled by Precision Dose Inc. Due to cGMP...
The Issue: cGMP Deviations: Product manufactured with contaminated raw ingredient.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Oral Suspension Recalled by Precision Dose Inc. Due to cGMP...
The Issue: cGMP Deviations: Product manufactured with contaminated raw ingredient.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hanger-Bar 2P 45cm Recalled by Human Care USA, Inc. Due to The Hanger-Bar is...
The Issue: The Hanger-Bar is being recalled due to the potential for the set screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hanger-Bar 2P 45cm Recalled by Human Care USA, Inc. Due to The Hanger-Bar is...
The Issue: The Hanger-Bar is being recalled due to the potential for the set screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....
The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...
The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...
The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....
The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol...
The Issue: When calibrating using the standard provided in the kit, the change in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renata Plant-Based Suprema Pizza Recalled by Mi Piace LLC Due to Undeclared Soy
The Issue: Undeclared soy allergen in frozen pizza
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diversatek Health Recalled by Diversatek Healthcare Due to M-Catch Retrieval...
The Issue: M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wireless Footswtich used with the following Philips Allura Xper and Recalled...
The Issue: Wireless foot switch connection issues causing interruption of Fluoroscopy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System:...
The Issue: The Instructions for Use have been updated to include: (1) Clarification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonidine Transdermal System Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MaryRuth's Organic Infants Liquid Probiotic Recalled by MARY RUTH ORGANICS...
The Issue: Internal testing found the presence of Pseudomonas aeruginosa in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.