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. 2,465 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,465 in last 12 months

Showing 3288132900 of 49,976 recalls

FoodAugust 9, 2016· Rabbit Creek Products Inc.

Recalled Item: White Chocolate Cranberry Quick Bread Mix Recalled by Rabbit Creek Products...

The Issue: Bread, muffin, and brownie mixes may have been manufactured with flour...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 9, 2016· Rabbit Creek Products Inc.

Recalled Item: Million Dollar Brownie Mix Recalled by Rabbit Creek Products Inc. Due to...

The Issue: Bread, muffin, and brownie mixes may have been manufactured with flour...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 8, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Calibrator U Recalled by Siemens Healthcare...

The Issue: Failure of analytical sensitivity with Calibrator U kit lots ending in 63...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Syringe Module Model 8110 with software version 9.15 The Recalled by...

The Issue: A software anomaly with the Alaris Syringe module software version 9.15 may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Arrow International Inc

Recalled Item: Arterial Line Catheterization Kit with Sharps Safety Features Permits access...

The Issue: Shipping carton labeling error.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Becton Dickinson & Company

Recalled Item: BD 23 G x .75 in. BD Vacutainer¿ Push Button Recalled by Becton Dickinson &...

The Issue: BD has received multiple reports of units associated with the 23 G x .75 in....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Nidek Inc

Recalled Item: SPECULAR MICROSCOPE CEM-530 Recalled by Nidek Inc Due to Software version...

The Issue: Software version 1.08 and 1.09 for the Specular Microscope CEM 530 included...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2016· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit with Sharps Safety Features Permits access...

The Issue: Shipping carton labeling error.

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Aller-Chlor (chlorpheniramine maleate) Syrup Recalled by Pharmatech LLC Due...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Diocto Syrup (docusate sodium) Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Sennazon (sennosides) Syrup Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Ninjacof (chlophedianol HCl and pyrilamine maleate) Liquid Recalled by...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Senexon Liquid (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Ninjacof-A (acetaminophen Recalled by Pharmatech LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2016· Pharmatech LLC

Recalled Item: Senna Syrup (sennosides) 8.8 mg Recalled by Pharmatech LLC Due to CGMP...

The Issue: CGMP Deviations: Recall initiated as a precautionary measure due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 5, 2016· Teva North America

Recalled Item: Claravis (isotretinoin capsules USP) Recalled by Teva North America Due to...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 5, 2016· Medtronic Inc.

Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...

The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.x picture archiving and communication system Syngo.x is a software...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Riverpoint Medical, LLC

Recalled Item: Polypropylene Surgical Sutures Recalled by Riverpoint Medical, LLC Due to...

The Issue: Polypropylene Surgical Sutures are recalled because the seals may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam and Symbia E gamma camera systems with patient beds Recalled by...

The Issue: "We have received reports of patients hair being caught in the e.cam and...

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

Class II — Potential Health HazardOngoing