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. 2,642 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,642 in last 12 months

Showing 91419160 of 28,654 recalls

Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: OctoStretch with Stretch Leveller - The combination of this products...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Elition X-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Ambition S-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T CX-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T- a Magnetic Resonance Medical Electrical Systems indicated for...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: SmartPath to dStream for XR and 3.0T-a Magnetic Resonance Medical Recalled...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Ambition X- Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 3.0T CX-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T Evolution-a Magnetic Resonance Medical Electrical Systems...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Elition S-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T S-a Magnetic Resonance Medical Electrical Systems indicated for...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: SmartPath to dStream for 1.5T-a Magnetic Resonance Medical Electrical...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Vitrectomy Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Ear Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Basic Cataract tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Newborn Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Core Biopsy Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Ultrasound Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Stereotactic Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing