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. 2,509 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,509 in last 12 months

Showing 2084120860 of 49,976 recalls

DrugSeptember 3, 2019· Coast Quality Pharmacy, LLC dba Anazao Health

Recalled Item: Clonidine HCL and Baclofen and Fentanyl Citrate in all strengths Recalled by...

The Issue: Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 3, 2019· GE Healthcare, LLC

Recalled Item: Achilles Express Bone Sonometer Recalled by GE Healthcare, LLC Due to...

The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2019· GE Healthcare, LLC

Recalled Item: Achilles Insight Bone Sonometer Recalled by GE Healthcare, LLC Due to...

The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...

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

Class II — Potential Health HazardOngoing
DrugAugust 30, 2019· Plastikon Healthcare LLC

Recalled Item: Milk of Magnesia USP Recalled by Plastikon Healthcare LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: product failed bioburden...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 30, 2019· Diamond Crystal Brands Inc

Recalled Item: Chef's Companion Instant Chocolate Mousse Mix Net Wt. 1 lb 14 oz (851 g)...

The Issue: Products were made with a cocoa powder that contained soy lecithin but soy...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2019· Diamond Crystal Brands Inc

Recalled Item: Madrona Market Delicatessen Hot Cocoa Mix Recalled by Diamond Crystal Brands...

The Issue: Products were made with a cocoa powder that contained soy lecithin but soy...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2019· Diamond Crystal Brands Inc

Recalled Item: Gridestone Cafe Swiss Style Cocoa Mix Recalled by Diamond Crystal Brands Inc...

The Issue: Products were made with a cocoa powder that contained soy lecithin but soy...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2019· Hiland Dairy Foods

Recalled Item: One-Half Gallon Hiland Dairy Lemonade packaged in plastic Recalled by Hiland...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 30, 2019· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Central Recalled by Spacelabs Healthcare, Inc. Due to The firm...

The Issue: The firm received reports of loss of audio alarm after a power failure or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S8-3t UDI (01)00884838073524 Can be used as Recalled by Philips...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S7-3t UDI (01)00884838061439 Can be used with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S8-3t UDI (01)00884838067523 Can be used with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S7-3t UDI (01)00884838067530 Used as accessory with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Pajunk GmbH

Recalled Item: SPROTTE Lumbar with Introducer Recalled by Pajunk GmbH Due to Problem with...

The Issue: Problem with packaging sealing process which affects sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· GE Healthcare, LLC

Recalled Item: ApexPro Telemetry Server System. Also identified as Modification To: ApexPro...

The Issue: May not provide visual and/or audible alarms at the CARESCAPE Central...

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

Class II — Potential Health HazardOngoing
DrugAugust 29, 2019· Johnson Matthey Inc.

Recalled Item: Fentanyl Citrate Active Pharmaceutical Ingredient Recalled by Johnson...

The Issue: cGMP Deviations: Potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2019· Johnson Matthey Inc.

Recalled Item: Cisplatin Active Pharmaceutical Ingredient Recalled by Johnson Matthey Inc....

The Issue: cGMP Deviations: Potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2019· Johnson Matthey Inc.

Recalled Item: Oxaliplatin Active Pharmaceutical Ingredient Recalled by Johnson Matthey...

The Issue: cGMP Deviations: Potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 29, 2019· LABSTYLE INNOVATIONS

Recalled Item: Dario Blood Glucose Monitoring System Recalled by LABSTYLE INNOVATIONS Due...

The Issue: The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may...

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

Class II — Potential Health HazardOngoing
DrugAugust 28, 2019· AVKARE Inc.

Recalled Item: AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg Recalled...

The Issue: Failed Stability Specifications.

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

Class II — Potential Health HazardOngoing
Refund