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. 2,641 recalls have been distributed to Oregon in the last 12 months.
Showing 7301–7320 of 13,369 recalls
Recalled Item: Hydromorphone Recalled by Pfizer Inc. Due to Non-Sterility: Confirmed...
The Issue: Non-Sterility: Confirmed customer complaints of glass product container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azelastine HCl Nasal Solution (Nasal Spray) 0.1% (137 mcg per spray)...
The Issue: Sun Pharmaceutical is recalling Azelastine HCl Nasal Solution, 0.1% (30 mL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORCO (Hydrocodone Bitartrate and Acetaminophen) Tablets Recalled by...
The Issue: Labeling: Not Elsewhere Classified: does not have the required "CII"...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Tablets Recalled by Aurobindo Pharma Ltd. Due to...
The Issue: Presence of Foreign Tablet: Metformin BP 1000mg was found in bottle of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VELCADE (bortezomib) for injection Recalled by Millennium Pharmaceuticals...
The Issue: Defective Container: Confirmed reports of loose vial crimps.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets 20 mg Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets 10 mg Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System. 75 mcg/h Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Megestrol Acetate Oral Suspension Recalled by Mckesson Packaging Services...
The Issue: Subpotent Drug: Out of specification for assay (stability testing)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System. 25 mcg/h Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications: Fentanyl-n-Oxide (FNO)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets 40 mg Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Impurities/Degradations Specifications; out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Limbrel (flavocoxid 500 mg) capsules Recalled by Primus Pharmaceuticals,...
The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Limbrel500 (flavocoxid and citrated zinc bisglycinate) 500 mg/50 mg capsules...
The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Limbrel250 (flavocoxid and citrated zinc bisglycinate) 250 mg/50 mg capsules...
The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Limbrel (flavocoxid 250 mg) capsules Recalled by Primus Pharmaceuticals,...
The Issue: Marketed Without An Approved NDA/ANDA: Based on the labeling claims, these...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets...
The Issue: CGMP deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefuroxime Recalled by JCB Laboratories LLC Due to Subpotent Drug: The...
The Issue: Subpotent Drug: The product is sub-potent prior to its 90-day beyond use date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mycamine (micafungin) for Injection 100 mg/vial Single-Dose Vial Rx only...
The Issue: Labeling: Label Error on Declared Strength
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.