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.

50,914 total recalls
2,641 in last 12 months

Showing 74017420 of 13,369 recalls

DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: Labetalol HCl in all strengths Recalled by Pharmedium Services, LLC Due to...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: Ketamine HCl in 0.9% Sodium Chloride in all strengths Recalled by Pharmedium...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: Dexamethasone Sodium Phosphate added to 0.9% Sodium Chloride in all...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: Bupivacaine HCl in 0.9% Sodium Chloride in all doses Recalled by Pharmedium...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: HYDROmorphone HCl Injection in all strengths Recalled by Pharmedium...

The Issue: Lack of sterility assurance.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2017· Hetero Labs Limited Unit V

Recalled Item: Famciclovir Tablets Recalled by Hetero Labs Limited Unit V Due to...

The Issue: Temperature Abuse: Complaints of tablets being wet and stuck together with...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2017· Hetero Labs, Ltd. - Unit III

Recalled Item: Simvastatin Tablets Recalled by Hetero Labs, Ltd. - Unit III Due to Presence...

The Issue: Presence of foreign substance: metallic razor blade was found in one bottle.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 21, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Clobetasol Propionate Cream USP Recalled by Taro Pharmaceuticals U.S.A.,...

The Issue: Failed Content Uniformity Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 20, 2017· Odan Laboratories Ltd

Recalled Item: Dry to Normal Skin Starter Kit Recalled by Odan Laboratories Ltd Due to...

The Issue: Failed Stability Specifications:stability failure at 12 months, long term RT...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2017· Odan Laboratories Ltd

Recalled Item: Day Cream SPF15 Cr¿me de jour FPS 15 Recalled by Odan Laboratories Ltd Due...

The Issue: Failed Stability Specifications:stability failure at 12 months, long term RT...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 19, 2017· Unichem Pharmaceuticals Usa Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets USP Recalled by Unichem...

The Issue: Cross Contamination With Other Products: metronidazole powder was found in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2017· Osmotica Pharmaceutical Corp

Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 18, 2017· Osmotica Pharmaceutical Corp

Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 15, 2017· Akorn Inc

Recalled Item: Gabapentin Oral Solution Recalled by Akorn Inc Due to CGMP Deviations:...

The Issue: CGMP Deviations: Inadvertent release of a drug product with unapproved...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 15, 2017· B. Braun Medical Inc

Recalled Item: 0.25% Acetic Acid Irrigation USP Recalled by B. Braun Medical Inc Due to...

The Issue: Presence of Particulate Matter: identified as polyethylene, which is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 15, 2017· Amneal Pharmaceuticals

Recalled Item: Fosphenytoin Sodium Injection Recalled by Amneal Pharmaceuticals Due to...

The Issue: Presence of particulate matter

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· Teva Pharmaceuticals USA

Recalled Item: Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP Recalled by...

The Issue: Failed Impurities/Degradation Specifications: High out of specification test...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Discovery Set contains SPF 50+ (octinoxate 4.9%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ Recalled...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund