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. 2,385 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,385 in last 12 months

Showing 4530145320 of 49,976 recalls

Medical DeviceJuly 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker TPS Universal Driver 99 Rx Recalled by Stryker Instruments Div. of...

The Issue: The safety margin values detailed in the Engineering Design were entered...

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

Class II — Potential Health HazardOngoing
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Nata Komplete Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: NataChew Recalled by Stayma Consulting Service, LLC. Due to Subpotent; Beta...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 430 ec Recalled by Stayma Consulting Service, LLC. Due to...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 430 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 400 Recalled by Stayma Consulting Service, LLC. Due to Subpotent;...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA Balanced Recalled by Stayma Consulting Service, LLC. Due to...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
DrugJune 28, 2013· Stayma Consulting Service, LLC.

Recalled Item: Duet DHA 400 ec Recalled by Stayma Consulting Service, LLC. Due to...

The Issue: Subpotent; Beta carotene (Vitamin A)

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

Class III — Low RiskOngoing
Refund
FoodJune 28, 2013· Priester Pecan Company, Inc.

Recalled Item: PRIESTER'S PECANS brand brand ROASTED SALTED PISTACHIOS Recalled by Priester...

The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 28, 2013· Priester Pecan Company, Inc.

Recalled Item: PRIESTER'S PECANS brand FANCY ROASTED NUTS Recalled by Priester Pecan...

The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 28, 2013· Priester Pecan Company, Inc.

Recalled Item: PRIESTER'S PECANS brand NUTTY FAVORITES ASST Recalled by Priester Pecan...

The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 28, 2013· Vinco Inc.

Recalled Item: Vinco's OsteoSheath 4 Enhanced Bone Support Recalled by Vinco Inc. Due to...

The Issue: The soy ingredient used to manufacture certain lots of Vinco's Osteosheath 4...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 28, 2013· Vinco Inc.

Recalled Item: Vinco's Fem-Vite Women's Anti-Oxidant Formula Recalled by Vinco Inc. Due to...

The Issue: The soy ingredient used to manufacture certain lots of Vinco's Fem-Vite was...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 28, 2013· Vinco Inc.

Recalled Item: Vinco's OsteoSheath Enhanced Bone Support Recalled by Vinco Inc. Due to...

The Issue: The soy ingredient used to manufacture certain lots of Vinco's Osteosheath...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 28, 2013· Alphatec Spine, Inc.

Recalled Item: Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico Recalled by...

The Issue: The firm initiated this recall of certain lots of Illico Ti Cannulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Calibrator A. Cat. #04800735 Recalled by Siemens Healthcare...

The Issue: Calibrator A lot CA77 is under-recovering to the assigned target for the...

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

Class III — Low RiskOngoing
Medical DeviceJune 28, 2013· Zimmer, Inc.

Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...

The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2013· Zimmer, Inc.

Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...

The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2013· Medtronic Neurosurgery

Recalled Item: Medtronic Preimplantation Test Kit Recalled by Medtronic Neurosurgery Due to...

The Issue: Medtronic Neurosurgery is recalling the Medtronic Preimplantation Test Kit...

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

Class II — Potential Health HazardOngoing
DrugJune 27, 2013· Fabscout Entertainment, Inc

Recalled Item: Silver Sword capsules Recalled by Fabscout Entertainment, Inc Due to...

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...

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

Class I — Serious Health HazardOngoing
Refund