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. 2,431 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,431 in last 12 months

Showing 3964139660 of 49,976 recalls

Medical DeviceJanuary 16, 2015· Halyard Health

Recalled Item: KimVent Closed Suction System for Adults Recalled by Halyard Health Due to...

The Issue: Defect: A hole or crack was found which may cause air to leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2015· CME America, LLC

Recalled Item: BodyGuard 323 pump Recalled by CME America, LLC Due to CME America is...

The Issue: CME America is recalling the BodyGuard and BodyGuard 323 Infusion pumps due...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists that the monitor may fail and requires a power circle...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2015· Brainlab AG

Recalled Item: The Brainlab Offset Cup Impactor Universal. Part of the Brainlab Recalled by...

The Issue: The recommended sterilization and drying parameters are not effective to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HeartWare Controller) Product Usage:...

The Issue: The affected clinical trial Controllers exhibit a higher susceptibility to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 16, 2015· Halyard Health

Recalled Item: KimVent Wet Pak Recalled by Halyard Health Due to Defect: A hole or crack...

The Issue: Defect: A hole or crack was found which may cause air to leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2015· Halyard Health

Recalled Item: KimVent Closed Suction System for Adults Recalled by Halyard Health Due to...

The Issue: Defect: A hole or crack was found which may cause air to leak.

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

Class II — Potential Health HazardOngoing
FoodJanuary 16, 2015· Aron Streit Inc.

Recalled Item: Streit's Kids Dark CHOCOLATE Coins Recalled by Aron Streit Inc. Due to...

The Issue: State of New York Department of Agriculture and Markets tested revealed...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2015· Brinkhoff & Monoson Inc

Recalled Item: Dark Chili Powder packaged in the following configurations: (1) a Recalled...

The Issue: The products contain cumin that may be contaminated with undeclared peanut...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2015· Brinkhoff & Monoson Inc

Recalled Item: Archer Farms Cumin Recalled by Brinkhoff & Monoson Inc Due to Undeclared Peanut

The Issue: The products contain cumin that may be contaminated with undeclared peanut...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2015· classic cooking llc

Recalled Item: Garden Lites Kale & Quinoa Souffle Recalled by classic cooking llc Due to...

The Issue: Cumin contains undeclared peanut protein

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2015· Brinkhoff & Monoson Inc

Recalled Item: HT Traders Blue Cheese Jalapeno Spicy & Unique Seasoning Blend Recalled by...

The Issue: The products contain cumin that may be contaminated with undeclared peanut...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2015· classic cooking llc

Recalled Item: classic cooking Kale and Quinoa Cake Recalled by classic cooking llc Due to...

The Issue: Cumin contains undeclared peanut protein

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2015· classic cooking llc

Recalled Item: Garden Lites Veggie Bites Kale & Brown Rice Recalled by classic cooking llc...

The Issue: Cumin contains undeclared peanut protein

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2015· classic cooking llc

Recalled Item: garden lites Southwestern Souffle Recalled by classic cooking llc Due to...

The Issue: Cumin contains undeclared peanut protein

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2015· classic cooking llc

Recalled Item: garden lites Veggie Chili & Cornbread Melt Recalled by classic cooking llc...

The Issue: Cumin contains undeclared peanut protein.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 15, 2015· Churchill Medical Systems, Inc.

Recalled Item: Bifircated Extension Set Recalled by Churchill Medical Systems, Inc. Due to...

The Issue: Potential for leaking caused by insufficient bond between needleless device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2015· Churchill Medical Systems, Inc.

Recalled Item: 6" Trifurcated set with Bionectors Recalled by Churchill Medical Systems,...

The Issue: Potential for leaking caused by insufficient bond between needleless device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2015· Churchill Medical Systems, Inc.

Recalled Item: 8" Standard Bore Ext Set Recalled by Churchill Medical Systems, Inc. Due to...

The Issue: Potential for leaking caused by insufficient bond between needleless device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2015· Churchill Medical Systems, Inc.

Recalled Item: 4" Microbore Trifurcated Ext set Recalled by Churchill Medical Systems, Inc....

The Issue: Potential for leaking caused by insufficient bond between needleless device...

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

Class II — Potential Health HazardOngoing