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. 2,379 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,379 in last 12 months

Showing 4696146980 of 49,976 recalls

FoodMarch 1, 2013· Jans Enterprises Corp. dba WIRA Corp.

Recalled Item: Jasmine Brand Garlic Flavored Crackers (Krupuk Bawang) Recalled by Jans...

The Issue: Wira Corp. is recalling Jasmine Garlic Flavored Crackers because of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bumble Bee International

Recalled Item: Bumble Bee Brand 5oz Chunk Light Tuna in Vegetable Oil Recalled by Bumble...

The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bumble Bee International

Recalled Item: Brunswick and Bumble Bee Brand 5oz Chunk Light Tuna in Water. Recalled by...

The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bumble Bee International

Recalled Item: Bumble Bee Brand 5oz Chunk White Albacore in Water Recalled by Bumble Bee...

The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bay Valley Foods LLC/ TreeHouse Foods, Inc

Recalled Item: 55613130643 Our Specialty Linguini & Parmesan Recalled by Bay Valley Foods...

The Issue: Bay Valley Foods is voluntarily recalling approximately 430,227 cases of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bay Valley Foods LLC/ TreeHouse Foods, Inc

Recalled Item: 55613210946 Western Family Recalled by Bay Valley Foods LLC/ TreeHouse...

The Issue: Bay Valley Foods is voluntarily recalling approximately 430,227 cases of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bay Valley Foods LLC/ TreeHouse Foods, Inc

Recalled Item: 556132100582 Meijer Recalled by Bay Valley Foods LLC/ TreeHouse Foods, Inc...

The Issue: Bay Valley Foods is voluntarily recalling approximately 430,227 cases of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bay Valley Foods LLC/ TreeHouse Foods, Inc

Recalled Item: 55613205218 Pasta on the Side Recalled by Bay Valley Foods LLC/ TreeHouse...

The Issue: Bay Valley Foods is voluntarily recalling approximately 430,227 cases of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 1, 2013· American Medical Systems, Inc.

Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...

The Issue: American Medical Systems, Inc. is initiating a recall on two components of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· American Medical Systems, Inc.

Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...

The Issue: American Medical Systems, Inc. is initiating a recall on two components of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· B. Braun Medical, Inc.

Recalled Item: Diacap(R) Ultra Dialysis Fluid Filter Recalled by B. Braun Medical, Inc. Due...

The Issue: There is the potential of the residual moisture of the Diacap Ultra membrane...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir Recalled...

The Issue: Certain lots of Reagent reservoirs, may not have a separation in the lower...

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

Class II — Potential Health HazardOngoing
FoodFebruary 28, 2013· See's Candies Inc.

Recalled Item: See's Candies Recalled by See's Candies Inc. Due to One code of 1.7 oz...

The Issue: One code of 1.7 oz Divinity Easter Eggs with Walnuts may actually contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 28, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mammomat Inspiration - full-field digital mammography Product Usage:...

The Issue: Firm became aware of an unintended behavior when using the Mammomat...

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

Class II — Potential Health HazardOngoing
DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: FIBRICOR (fenofibric acid) Tablets Recalled by Mutual Pharmaceutical...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2013· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Labeling Wrong Barcode; It may display wrong product code 0.9% Sodium...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2013· Hospira Inc.

Recalled Item: The PCA 3 infusion pump allows clinicians Recalled by Hospira Inc. Due to...

The Issue: The infusion pump has a clear plastic door that, due to its design, allows...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2013· Hospira Inc.

Recalled Item: The LifeCare PCA infusion system with Hospira MedNet software allows...

The Issue: The infusion pump has a clear plastic door that, due to its design, allows...

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

Class II — Potential Health HazardOngoing