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. 2,592 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,592 in last 12 months

Showing 1430114320 of 49,976 recalls

Medical DeviceOctober 15, 2021· GE Healthcare, LLC

Recalled Item: GE Centricity Universal Viewer Zero Footprint Client Recalled by GE...

The Issue: There is a potential to display incomplete patient imaging study.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2021· Medtronic Vascular, Inc.

Recalled Item: Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT...

The Issue: Due to, during stent graft deployment, the spindle may detach from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2021· Medtronic Vascular, Inc.

Recalled Item: Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT...

The Issue: During stent graft deployment, the spindle may detach from the distal end of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2021· Medtronic Vascular, Inc.

Recalled Item: Endurant IIs Stent Graft System REF/Description: ESBF2814C103EE STENT GRAFT...

The Issue: Due to, during stent graft deployment, the spindle may detach from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products Anti-HBc IgM Controls Recalled by...

The Issue: Ortho Clinical Diagnostics confirmed a complaint that some VITROS...

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

Class III — Low RiskOngoing
FoodOctober 14, 2021· KEURIG DR PEPPER

Recalled Item: Target Good & Gather Coconut Pineapple Sparkling Water 8 pack Recalled by...

The Issue: The company has received off flavor and off aroma complaints identified with...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 14, 2021· KEURIG DR PEPPER

Recalled Item: 7UP Zero Sugar Lemon Lime Soda 12 pack of 12 Recalled by KEURIG DR PEPPER...

The Issue: The company has received off flavor and off aroma complaints identified with...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 14, 2021· KEURIG DR PEPPER

Recalled Item: Polar Black Cherry Premium Seltzer 12 pack of 12oz cans Recalled by KEURIG...

The Issue: The company has received off flavor and off aroma complaints identified with...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 14, 2021· KEURIG DR PEPPER

Recalled Item: Target Good & Gather Mixed Berry Sparkling Water 8 pack Recalled by KEURIG...

The Issue: The company has received off flavor and off aroma complaints identified with...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 14, 2021· SEDECAL SA

Recalled Item: MobileDiagnost wDR Recalled by SEDECAL SA Due to While cleaning or...

The Issue: While cleaning or disinfecting the system, if the process is not followed as...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2021· Hill-Rom Inc.

Recalled Item: These are communication systems Recalled by Hill-Rom Inc. Due to An...

The Issue: An unrecoverable error may occur where a component will fail to complete the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2021· Lumenis, Inc.

Recalled Item: IPL Coupling Gel Recalled by Lumenis, Inc. Due to Ultrasound gels and...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 14, 2021· FujiFilm Healthcare Americas Corporation

Recalled Item: Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3 Recalled by...

The Issue: Diagnostic ultrasound system with the specified software version and used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2021· FujiFilm Healthcare Americas Corporation

Recalled Item: Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3 Recalled by...

The Issue: Diagnostic ultrasound system with the specified software version and used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2021· FujiFilm Healthcare Americas Corporation

Recalled Item: Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3 Recalled by...

The Issue: Diagnostic ultrasound system with the specified software version and used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2021· FujiFilm Healthcare Americas Corporation

Recalled Item: Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0 Recalled by...

The Issue: When the ultrasound system is used in combination with a Fujifilm (formally...

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

Class II — Potential Health HazardOngoing
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: Advance Formula Pain Reliever (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: Afassco Pain Free Plus X-STRENGTH PAIN RELIEVER (Acetaminophen 250...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg Recalled by...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund