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. 2,680 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,680 in last 12 months

Showing 25812600 of 49,976 recalls

FoodApril 17, 2025· May Flower International Inc

Recalled Item: Beijing Soybean Paste Recalled by May Flower International Inc Due to...

The Issue: Product contains undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: Ropivacaine Hydrochloride Injection Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard¿ Single Intragastric Linton Balloon Tube Recalled by C.R. Bard Inc Due...

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· Cook Incorporated

Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2025· Cook Incorporated

Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...

The Issue: Cook Medical identified that devices from the affected device lots may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) Recalled by C.R....

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) Recalled by C.R. Bard...

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard Minnesota Four Lumen Esophagogastric Tamponade Tube Recalled by C.R....

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· C.R. Bard Inc

Recalled Item: Bard Blakemore Esophageal-Nasogastric Tube (Adult) Recalled by C.R. Bard Inc...

The Issue: Due to customer complaints, there is a potential for users to be unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2025· Straumann USA LLC

Recalled Item: WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments....

The Issue: Incorrect blister labelling.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2025· Luminex Corporation

Recalled Item: VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test Recalled by...

The Issue: It was determined that the consumable issue may result in No Call - INT CTL...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2025· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus Pro Patient Monitor Recalled by Remote Diagnostic Technologies Ltd....

The Issue: software issue that causes an error screen on a portable vital signs monitor...

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

Class II — Potential Health HazardOngoing
FoodApril 15, 2025· Optimal Carnivore, LLC

Recalled Item: Bone & Joint Restore. 180 capsules in a plastic bottle. Recalled by Optimal...

The Issue: Potential for contamination with salmonella.

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2025· OurPharma LLC

Recalled Item: HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL) Recalled by OurPharma LLC Due...

The Issue: Superpotent Drug: Assay/potency result for hydromorphone HCl in the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 15, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number:...

The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376....

The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2025· Remote Diagnostic Technologies Ltd.

Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...

The Issue: Patient Monitor software update to address issues:1)May freeze at startup...

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

Class II — Potential Health HazardOngoing
DrugApril 14, 2025· SAINI TRADE INC

Recalled Item: ELECTRO BUZZ Recalled by SAINI TRADE INC Due to Undeclared Chloropretadalafil

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 14, 2025· SAINI TRADE INC

Recalled Item: ULTRA ARMOR Recalled by SAINI TRADE INC Due to Undeclared...

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 14, 2025· SAINI TRADE INC

Recalled Item: Male Ultra Pro Recalled by SAINI TRADE INC Due to Undeclared...

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...

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

Class I — Serious Health HazardOngoing
Refund