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 3960139620 of 49,976 recalls

Medical DeviceJanuary 27, 2015· GE Healthcare

Recalled Item: GE Healthcare Engstrom Carestation Recalled by GE Healthcare Due to...

The Issue: Potential failure of the caster mounting hardware, which may result in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...

The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...

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

Class II — Potential Health HazardOngoing
DrugJanuary 26, 2015· AnazaoHealth Corporation

Recalled Item: Compounded Plaquex Recalled by AnazaoHealth Corporation Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an active...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: MediChoice WarmGel Infant Heel Warmer Recalled by CooperSurgical, Inc. Due...

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: CooperSurgical Infant Heel Gel Warmers Recalled by CooperSurgical, Inc. Due...

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: Fisher Brand Gel Infant Heel Gel Warmers Recalled by CooperSurgical, Inc....

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2015· CooperSurgical, Inc.

Recalled Item: NovaPlus Brand Warm Gel Infant Heel Gel Warmer Recalled by CooperSurgical,...

The Issue: Products without expiration date have the remote potential for minor burn

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

Class II — Potential Health HazardOngoing
DrugJanuary 25, 2015· Detox Transforms

Recalled Item: EDGE Amplified Weight Release capsules Recalled by Detox Transforms Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 25, 2015· Detox Transforms

Recalled Item: BtRiM Max capsules Recalled by Detox Transforms Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 25, 2015· Detox Transforms

Recalled Item: iNDiGO capsules Recalled by Detox Transforms Due to Undeclared Phenolphthalein

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 25, 2015· Detox Transforms

Recalled Item: AMPD GOLD Bee Pollen capsules Recalled by Detox Transforms Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 25, 2015· Detox Transforms

Recalled Item: iNSANE Bee Pollen capsules Recalled by Detox Transforms Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 23, 2015· Hospira Inc.

Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 23, 2015· Hospira Inc.

Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 23, 2015· Mylan Institutional LLC

Recalled Item: Nicardipine Hydrochloride Injection Recalled by Mylan Institutional LLC Due...

The Issue: Subpotent Drug and Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
FoodJanuary 23, 2015· Korean Food Co.

Recalled Item: Go hyang Mak Kimchi 32 oz () Product of Recalled by Korean Food Co. Due to...

The Issue: Product contains undeclared shellfish (shrimp)

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 23, 2015· Probar LLC

Recalled Item: PROBAR Frosted Peanut Butter BASE Protein Bar Recalled by Probar LLC Due to...

The Issue: PROBAR, LLC has initiated a voluntary recall of its PROBAR Base Frosted...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 23, 2015· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Passport V Monitor Recalled by Mindray DS USA, Inc. dba Mindray North...

The Issue: An issue has been identified with Passport V Monitors invasive blood...

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

Class II — Potential Health HazardOngoing