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. 2,404 recalls have been distributed to Oregon in the last 12 months.
Showing 43061–43080 of 50,914 recalls
Recalled Item: MIC PLUS B12 Recalled by John W Hollis Inc Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Papaverine HCl 30 mg Recalled by John W Hollis Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mannitol 5% Solution for injection Recalled by John W Hollis Inc Due to Lack...
The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polidocanol 1% Solution for Injection Recalled by John W Hollis Inc Due to...
The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate for Injection Recalled by John W Hollis Inc Due to...
The Issue: Lack of Assurance of Sterility: Lack of sterility assurance in compounded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000...
The Issue: Physio-Control has become aware of incidents where customers have attempted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilett XP Digital Mobile X-ray System Product Usage: The Recalled...
The Issue: There is a potential fire hazard of certain Lithium-Ion batteries in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Ventilator Flexport Interface Recalled by Spacelabs...
The Issue: Spacelabs Healthcare is voluntarily recalling the Hamilton Galileo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Ysio Systems Product Usage: The Ysio (New RAD-FAMILY) systems...
The Issue: Excessive usage of cleaning liquid on Siemens Ysio Systems may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marissa Collection Tangerine Appetizer Plate Set (set of 2). distributed...
The Issue: Plates leaching cadmium above the specified acceptable level
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Anspach Pneumatic and Electric Motor Systems. Intended for cutting and...
The Issue: Several attachments and handpieces failed to meet the expected sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Devon Supine Recalled by Covidien LLC Due to Straps may separate from the...
The Issue: Straps may separate from the foam pad.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACROLYTE Premie Dispersive Electrode Recalled by ConMed Corporation Due to...
The Issue: ConMed Corporation has received complaints regarding sparking, no output and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROMETHAZINE HYDROCHLORIDE Tablets Recalled by Zydus Pharmaceuticals USA Inc...
The Issue: Presence of Foreign Tablets: Presence of atenolol 25 mg tablet mixed into...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Rod Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Post Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens LANTIS System Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There is a potential risk when using LANTIS OIS System client software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visitec Anterior Chamber Cannula Recalled by Beaver-Visitec International...
The Issue: Contains a sharp tip needle when the product should contain a blunt tip cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVOCATE Redi-Code+ BMB-BA006A Blood Glucose test strips Product Usage: The...
The Issue: "Advocate Redi-Code + BMB-BA006A Blood Glucose test strips" are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Medical Imaging It is a medical image and information Recalled by...
The Issue: The firm has identified a software issue which may cause a discrepancy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.