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 31161–31180 of 50,914 recalls
Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...
The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metronidazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is...
The Issue: Product shipped proximate to or past the expiration date listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...
The Issue: In April 2015, HeartWare, now a part of Medtronic, notified users of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW Recalled by Smith &...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...
The Issue: The expiration dates on the labeling are incorrect, the actual expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURESTEP Tray Recalled by C.R. Bard, Inc. Due to Misbranded: Product...
The Issue: Misbranded: Product labeled, Not made with natural rubber latex, may in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: hydrALAZINE HYDROCHLORIDE INJECTION Recalled by Mckesson Medical Surgical...
The Issue: Temperature Abuse: Certain pieces of these lots distributed by McKesson...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone 40 mg/mL 2 mL Single-Dose Vial for Injection Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gerber¿ Pasta Pick-Ups Cheese Ravioli Net Wt 6 oz (170g) Recalled by Gerber...
The Issue: Gerber Products Company is recalling Cheese Ravioli Gerber¿ Pasta Pick-Ups¿...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 03896216 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 02419937 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 09010686 Recalled by Siemens...
The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adalat CC (nifedipine) Extended Release Tablets 30 mg Recalled by Alvogen,...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adalat CC (nifedipine) Extended Release Tablets Recalled by Alvogen, Inc Due...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...
The Issue: Cross Contamination with another product:residual powder found in inlet air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.