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. 2,486 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,486 in last 12 months

Showing 2402124040 of 50,914 recalls

Medical DeviceDecember 10, 2018· Signature Orthopedics Pty Limited

Recalled Item: Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement...

The Issue: Product mix up

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 7, 2018· US Pharmaceuticals Inc.

Recalled Item: Soothe & Cool Protect Moisture Guard Skin Protectant (petrolatum 59%)...

The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2018· US Pharmaceuticals Inc.

Recalled Item: Medline Remedy Essential Barrier Skin Protectant Ointment (petrolatum 59%)...

The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2018· US Pharmaceuticals Inc.

Recalled Item: Hydrocortisone Cream 1% MS Anti itch Cream with Intensive Healing 2 oz tubes...

The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Absorica (Isotretinoin) Capsules 30 mg USP Recalled by Sun Pharmaceutical...

The Issue: Subpotent Drug: Isotretinoin content results were lower than the...

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

Class III — Low RiskOngoing
Refund
FoodDecember 7, 2018· Threshold Enterprises Ltd

Recalled Item: Planetary Herbals Mullein Lung Complex Recalled by Threshold Enterprises Ltd...

The Issue: Recall of Mullein Lung Complex due to a labeling error which indicates the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 7, 2018· Moonstruck Chocolate Company

Recalled Item: The Salty Nutty Toffee Bar Recalled by Moonstruck Chocolate Company Due to...

The Issue: the Salty Nutty Toffee Bar is recalled due to undeclared soy lecithin

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: SiemensADVIA Centaur aTG (500 test kit) Siemens Material Number (SMN):...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Atellica IM aTG (100 test kit) Siemens Material Number (SMN):...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM aTG (500 test kit) Siemens Material Number (SMN): 10995462...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur aTG (100 test kit) Siemens Material Number Recalled by...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK STEM with Microporous Surface MP Reconstruction Prosthesis Recalled by...

The Issue: The reaming guide and the guide rod can't be screwed into the intended...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Ethicon Endo-Surgery Inc

Recalled Item: PROXIMATE¿ PPH Hemorrhoidal Circular Stapler Product Code:PPH03 PPH03: The...

The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Ethicon Endo-Surgery Inc

Recalled Item: PROXIMATE¿ HCS Hemorrhoidal Circular Stapler Product Code: PPH01 PPH01: The...

The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 6, 2018· Pfizer Inc.

Recalled Item: Levoxyl (levothyroxine sodium tablets Recalled by Pfizer Inc. Due to...

The Issue: Superpotent Drug.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 6, 2018· Carl Zeiss Meditec, Inc.

Recalled Item: VisuMax Software Version 2.10.13 with activated Software-Module ReLEx...

The Issue: VisuMax devices with software version 2.10.13 and activated SW-Module ReLEx...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2018· Medtronic Navigation, Inc.

Recalled Item: Medtronic Adapter Percutaneous Pin Recalled by Medtronic Navigation, Inc....

The Issue: Under certain circumstances, the percutaneous pin adapter used with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2018· Vygon U.S.A.

Recalled Item: Vygon DUALSTOP Red Cap used for intravascular lines Product Code: Recalled...

The Issue: DualStop Caps defect causing leaks in affected product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2018· Vygon U.S.A.

Recalled Item: Vyon DUALSTOP White Cap used for intravascular lines Product Code: Recalled...

The Issue: DualStop Caps defect causing leaks in affected product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2018· Bard Medical Division

Recalled Item: BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature...

The Issue: Some SureStep" Foley Tray Systems with product catalog number A319418AM and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing