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. 2,378 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,378 in last 12 months

Showing 4802148040 of 49,976 recalls

FoodSeptember 25, 2012· Falcon Trading Co., Inc.

Recalled Item: SunRidge Organic Crunchy Peanut Butter with salt Packed in 35 Recalled by...

The Issue: Falcon Trading Company Inc. used peanut butter in their products that is now...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 25, 2012· Falcon Trading Co., Inc.

Recalled Item: SunRidge Candy - Peanut Butter Power Chews. Packed in 10 Recalled by Falcon...

The Issue: Falcon Trading Company Inc. used peanut butter in their products that is now...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 25, 2012· Falcon Trading Co., Inc.

Recalled Item: SunRidge Chocolate Double Decker Chew Packed in 10 pound case. Recalled by...

The Issue: Falcon Trading Company Inc. used peanut butter in their products that is now...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 25, 2012· Falcon Trading Co., Inc.

Recalled Item: SunRidge Candy - Energy Nuggets Recalled by Falcon Trading Co., Inc. Due to...

The Issue: Falcon Trading Company Inc. used peanut butter in their products that is now...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 25, 2012· Chattanooga Bakery Inc

Recalled Item: Moon Pie(R) Crunch Peanut Butter Recalled by Chattanooga Bakery Inc Due to...

The Issue: Peanut Butter Crunch Moon Pies were manufactured with peanut butter supplied...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 25, 2012· Stryker Communications, Inc.

Recalled Item: (l) Visum Halogen Surgical Light Recalled by Stryker Communications, Inc....

The Issue: Stryker has become aware that there is a low likelihood of incomplete...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Alphatec Spine, Inc.

Recalled Item: ILLlCO¿ MIS Posterior Fixation System Recalled by Alphatec Spine, Inc. Due...

The Issue: The firm initiated the recall because the stainless steel guide-wire of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Belmont Instrument Corporation

Recalled Item: Belmont Rapid Infuser Recalled by Belmont Instrument Corporation Due to Leak...

The Issue: Leak from a saline bag caused saline to drip along the back of the Rapid...

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

Class II — Potential Health HazardOngoing