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 13411360 of 28,654 recalls

Medical DeviceJuly 3, 2025· Orascoptic Surgical Acuity

Recalled Item: Orascoptic Superior Visualization Phantom Essential kit ( Nose pad Recalled...

The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: X7-2t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Orascoptic Surgical Acuity

Recalled Item: Orascoptic Superior Visualization Custom loupes configured with Phantom...

The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: mC12-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: S7-3t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L17-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: S8-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: 7.5MHZ Endo Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Orascoptic Surgical Acuity

Recalled Item: Orascoptic Superior Visualization Phantom Nose Pad Accessory Kit ( nose...

The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: mL26-8 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C6-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: eL18-4 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: S12-4 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: S7-2t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L8-4 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L10-4LAP Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C10-4ec Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L18-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Orascoptic Surgical Acuity

Recalled Item: Orascoptic Superior Visualization Dragonfly Nose Pad Accessory Kit ( nose...

The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: V6-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing