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. 1,070 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
1,070 in last 12 months

Showing 15461–15480 of 49,976 recalls

Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Transport Stretcher 747 - a non-powered Recalled by Stryker Medical Division...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: CUB Pediatric Crib- intended to provide a pediatric patient support Recalled...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime TC-transport chair intended for medical purposes to assist a Recalled...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Stretcher Chair-for use in all acute care hospitals and medical Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: ComfortGel - assists in the prevention and treatment of all Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: GoBed II MedSurg Bed Recalled by Stryker Medical Division of Stryker...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: IsoGel Air - support surface assists in the prevention and Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...

The Issue: Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 12, 2021· American Health Packaging

Recalled Item: Sirolimus Tablets 1 mg Recalled by American Health Packaging Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...

The Issue: Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...

The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...

The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED ANTIMICROBIAL Hand Sanitizer Gel with Aloe Vera Recalled by...

The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...

The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 12, 2021· Hi Tech Pharmaceuticals

Recalled Item: Lipodrene With 25mg Ephedra Extract 100CT Recalled by Hi Tech...

The Issue: The firm was notified by the FDA that the product contains the unapproved...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: novaplus Recalled by Medical Action Industries, Inc. 306 Due to There is a...

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Skytron, Div. The KMW Group, Inc

Recalled Item: Skyton Bracket Flatscreen Recalled by Skytron, Div. The KMW Group, Inc Due...

The Issue: Failure of the FS32 Monitor Brackets from the mounting block could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Exactech, Inc.

Recalled Item: Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT....

The Issue: The HAT trial contains a retaining ring that has shown the potential to...

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

Class II — Potential Health HazardOngoing