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. 1,141 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
1,141 in last 12 months

Showing 861–880 of 49,976 recalls

Medical DeviceOctober 31, 2025· Philips Ultrasound, LLC

Recalled Item: Lumify Diagnostic Ultrasound System models : 795005 Recalled by Philips...

The Issue: Ultrasound system compatibility issues with Apple devices running iOS 18 may...

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: Dynagel Recalled by Blossom Pharmaceuticals Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Blossom Pharmaceuticals

Recalled Item: WeCare Recalled by Blossom Pharmaceuticals Due to cGMP deviations

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP30. Product Number: M8002A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP50. Product Number: M8004A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX850. Product Number: 866470. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX400. Product Number: 866060. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Aizu Olympus Co., Ltd.

Recalled Item: Olympus OER-Pro Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...

The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: darby dental supply Recalled by Novocol Pharmaceutical of Canada, Inc. Due...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: Benco dental Graham CHEMICAL CO. Recalled by Novocol Pharmaceutical of...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP90. Product Number: M8010A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP2. Product Number: M8102A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP80. Product Number: M8008A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: 3% Polocaine DENTAL Recalled by Novocol Pharmaceutical of Canada, Inc. Due...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: Lidocaine HCI 2% and Epinephrine 1:100 Recalled by Novocol Pharmaceutical of...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Multi Measurement Server X2. Product Number: M3002A. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
FoodOctober 31, 2025· HANA GROUP

Recalled Item: Mai California Roll WR - .9 oz (167g) Recalled by HANA GROUP Due to Wheat...

The Issue: Wheat and Soy missing allergens from the product Contains Statement.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX550. Product Number: 866066. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
FoodOctober 31, 2025· Blonde Beard's

Recalled Item: Blonde Beard's Dojo Asian Wing Sauce Recalled by Blonde Beard's Due to...

The Issue: Undeclared Soy

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2025· Novocol Pharmaceutical of Canada, Inc.

Recalled Item: Cook-Walte Recalled by Novocol Pharmaceutical of Canada, Inc. Due to...

The Issue: Defective container: cracked/broken cartridges

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

Class II — Potential Health HazardOngoing
Refund