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. 2,480 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,480 in last 12 months

Showing 2584125860 of 49,976 recalls

Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips Medical Systems Gmbh, DMC Due to...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Upgrades (Stitching Patient Support) 712083 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Monitor with one Blood Parameter Module and one HSat Probe Recalled by...

The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood parameter monitoring system 500 H/SAT Recalled by Terumo...

The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...

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

Class II — Potential Health HazardOngoing
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Recalled by World Organix, LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· MAJOR PHARMACEUTICALS

Recalled Item: Enalapril Maleate Tablets Recalled by MAJOR PHARMACEUTICALS Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Sub-recall because this...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Gold Series Ultra Enhanced Indo Recalled by World Organix,...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Kratom+CBD CBD infused Maeng Da Recalled by World Organix,...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 26, 2018· MAJOR PHARMACEUTICALS

Recalled Item: Enalapril Maleate Tablets Recalled by MAJOR PHARMACEUTICALS Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Sub-recall because this...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2018· World Organix, LLC

Recalled Item: Blissful Remedies Red Maeng Da Recalled by World Organix, LLC Due to...

The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...

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

Class I — Serious Health HazardOngoing
Refund