Product Recalls in Oklahoma

Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,496 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,496 in last 12 months

Showing 2374123760 of 49,976 recalls

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
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
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· 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· 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
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· 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 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· 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
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· Hologic, Inc.

Recalled Item: I-View¿ Contrast Enhanced Digital Mammography Recalled by Hologic, Inc. Due...

The Issue: Calibration issue not possible to visualize contrast uptake in 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: 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
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
DrugDecember 5, 2018· Pharmedium Services, LLC

Recalled Item: Fentanyl Citrate 2 mcg per mL (100 mcg per 50 Recalled by Pharmedium...

The Issue: Sub-potent

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2018· Pharmedium Services, LLC

Recalled Item: Fentanyl Citrate 2 mcg per mL (200 mcg per 100 Recalled by Pharmedium...

The Issue: Sub-potent

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 5, 2018· Medela Inc

Recalled Item: Breast Milk Transfer Lid for use with Oral Syringe Connectors Model:...

The Issue: The sterility may be compromised due to a potential breach in the packaging,...

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

Class III — Low RiskOngoing
Medical DeviceDecember 5, 2018· Sage Products Inc

Recalled Item: Toothete Oral Care Sodium Bicarbonate Mouthpaste Recalled by Sage Products...

The Issue: A voluntary recall of a lot (67924) of Independent Care System due to the...

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

Class II — Potential Health HazardOngoing