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. 2,511 recalls have been distributed to Oregon in the last 12 months.
Showing 20461–20480 of 50,914 recalls
Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 60 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 30 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 100 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% SODIUM CHLORIDE INJECTION Recalled by ICU Medical Inc Due to Presence...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LACTATED RINGER'S Injection Recalled by ICU Medical Inc Due to Presence of...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument - Product Usage: The...
The Issue: During the firm's review of May 2019 complaint data, a significant increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Knee Replacement System Model Number: TCR-111-1111-010102 -...
The Issue: Medial and lateral polyethylene inserts did not securely fit into the cobalt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taspen's Organics Respiratory Tea Recalled by Green Water, LLC Due to The...
The Issue: The products contain Coltsfoot, which is not to be used internally.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement Recalled...
The Issue: The products contain Coltsfoot, which is not to be used internally.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dragonfly Botanicals Full spectrum Breathe Deep 1000mg/oz Dietary Supplement...
The Issue: The products contain Coltsfoot, which is not to be used internally.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Python Embolectomy Catheters Recalled by Applied Medical Resources Corp Due...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical Dual Lumen Graft Cleaning Catheter & 1cc SYRINGE...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Embolectomy Catheter & 1 ml SYRINGE Recalled by Applied Medical...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene...
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide....
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rebel Monorail PtCr Coronary Stent System Recalled by Boston Scientific...
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide....
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - Recalled by...
The Issue: Sterile packaging incomplete seals may compromise sterility of the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...
The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.