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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,468 in last 12 months

Showing 3038130400 of 49,976 recalls

Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 7245C Recalled by Pentax of America Inc Due to Pentax Medical did not always...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· BioMerieux SA

Recalled Item: ETEST OXACILLIN OX 256 US F100 In vitro diagnostic Recalled by BioMerieux SA...

The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· BioMerieux SA

Recalled Item: ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic Recalled by BioMerieux SA...

The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic PAK NEEDLE BEVELED AND TROCAR TIPS Recalled by Medtronic Sofamor...

The Issue: Product packaging may incorrectly include two bevel-tipped needles or two...

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

Class II — Potential Health HazardOngoing
DrugApril 13, 2017· Spectrum Laboratory Products, Inc.

Recalled Item: Estradiol (17-B-Estradiol Recalled by Spectrum Laboratory Products, Inc. Due...

The Issue: CGMP Deviations: these repackaged and redistributed products are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2017· Standard Homeopathic Company

Recalled Item: Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS...

The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2017· Spectrum Laboratory Products, Inc.

Recalled Item: Levonorgestrel Recalled by Spectrum Laboratory Products, Inc. Due to CGMP...

The Issue: CGMP Deviations: these repackaged and redistributed products are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2017· Standard Homeopathic Company

Recalled Item: Hyland's Baby Teething Tablets [Calcarea Phosporica 6X HPUS Recalled by...

The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 12, 2017· XTANT MEDICAL INC

Recalled Item: 5.5mm Diameter x 500mm CoCr Straight Rod Recalled by XTANT MEDICAL INC Due...

The Issue: The material type on the label may incorrectly state Ti6Al-4V ELI. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure

Recalled Item: Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Recalled by...

The Issue: An unexpected transient mode switch behavior was detected by Medtronic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Vascular Solutions, Inc.

Recalled Item: Dolphin Inflation Device Recalled by Vascular Solutions, Inc. Due to The...

The Issue: The manufacturer of the DOLPHIN inflation device, Perouse Medical, has...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Datascope Corporation

Recalled Item: SENSATION PLUS¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit...

The Issue: Maquet/Getinge is initiating a voluntary product removal involving four lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Sensis Recalled by Siemens Medical Solutions USA, Inc Due to An...

The Issue: An extremely dusty computer can cause problems at system start, or rarely,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Sorin Group Italia SRL - CRF

Recalled Item: PARADYM Models: VR 8250 Recalled by Sorin Group Italia SRL - CRF Due to...

The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Sorin Group Italia SRL - CRF

Recalled Item: OVATIO Models: VR 6250 Recalled by Sorin Group Italia SRL - CRF Due to Sorin...

The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Sorin Group Italia SRL - CRF

Recalled Item: INTENSIA Models: VR 124 Recalled by Sorin Group Italia SRL - CRF Due to...

The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...

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

Class II — Potential Health HazardOngoing
FoodApril 11, 2017· Jimmy's Cookies

Recalled Item: The Bakery Peanut Butter Chocolate Chunk Cookies Recalled by Jimmy's Cookies...

The Issue: The Bakery Peanut Butter Chocolate Chunk Cookies may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 10, 2017· Vertical Pharmaceuticals, Inc.

Recalled Item: Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin Recalled...

The Issue: One (1) lot (21511158) of the OB Complete DHA is being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 10, 2017· B Braun Medical Inc

Recalled Item: CytoGuard Closed Luer Connector Recalled by B Braun Medical Inc Due to B....

The Issue: B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2017· bioMerieux, Inc.

Recalled Item: eMAG System Recalled by bioMerieux, Inc. Due to Some anomalies have been...

The Issue: Some anomalies have been identified during manufacturing controls.

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

Class II — Potential Health HazardOngoing