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. 2,654 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,654 in last 12 months

Showing 62616280 of 49,976 recalls

DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: The GOAT SUBLINGUAL STRIP Recalled by Pyramids Wholesale Inc. Due to...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: libigrow RED DRAGON+ Recalled by Pyramids Wholesale Inc. Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: GoHARD 25000 Recalled by Pyramids Wholesale Inc. Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 19, 2024· TriMed Inc.

Recalled Item: TriMed Recalled by TriMed Inc. Due to Nail system contains an out of...

The Issue: Nail system contains an out of specification driver-socket which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2024· TriMed Inc.

Recalled Item: TriMed Recalled by TriMed Inc. Due to Nail system contains an out of...

The Issue: Nail system contains an out of specification driver-socket which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: LifeVentEVO2 Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Aeris EVO Recalled by Philips Respironics, Inc. Due to Potential for sudden...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Garbin EVO Recalled by Philips Respironics, Inc. Due to Potential for sudden...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Allia IGS 7 OR Recalled by GE Medical Systems, SCS Due to GE...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Interact Discovery RT Recalled by GE Medical Systems, SCS Due...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Innova IGS 5 Recalled by GE Medical Systems, SCS Due to GE...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Allia IGS 7 Recalled by GE Medical Systems, SCS Due to GE...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Innova IGS 6 Recalled by GE Medical Systems, SCS Due to GE...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· XENEX Disinfection Services Inc.

Recalled Item: LightStrike Blackout Curtains Recalled by XENEX Disinfection Services Inc....

The Issue: Blackout curtains are no longer recommended as a protective barrier against...

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

Class II — Potential Health HazardOngoing