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. 2,588 recalls have been distributed to Oregon in the last 12 months.
Showing 14861–14880 of 50,914 recalls
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium ADVANTA VXT Vascular Graft Recalled by Atrium Medical Corporation Due...
The Issue: The product package may potentially contain a mismatched graft that does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnisound Gel Recalled by Accelerated Care Plus Corporation Due to...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating room table - Product Usage: intended for use during Recalled by...
The Issue: ORT200/300 rotational lock may fail to function such that it cannot change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rompe Pecho Max Multi-Symptoms Maximum Strength Recalled by Efficient...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rompe Pecho Ex Expectorant Recalled by Efficient Laboratories, Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rompe Pecho CF Cold & Flu Advanced Formula Recalled by Efficient...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rompe Pecho DM Recalled by Efficient Laboratories, Inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Firvanq (vancomycin hydrochloride for oral solution) Recalled by Azurity...
The Issue: Product Mix-up: Incorrect diluent component included in the kit.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch Recalled by...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch Recalled by...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...
The Issue: Potential for difficulty in safety mechanism activation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl Recalled by...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Recalled by National...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...
The Issue: Potential for a wire protrusion through the left heart vent catheter tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...
The Issue: Potential for a wire protrusion through the left heart vent catheter tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.