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. 2,590 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,590 in last 12 months

Showing 1534115360 of 49,976 recalls

FoodMay 27, 2021· Tiger Nuts

Recalled Item: Tiger Nuts Flour - 2.2 lbs. (1 Kilo) boxes Recalled by Tiger Nuts Due to...

The Issue: Product may be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 27, 2021· Cytocell Ltd.

Recalled Item: Cytocell LPH019-A E2A (TCF3) Breakapart Probe- In Vitro Diagnostic Analyte...

The Issue: May show unexpected locus specific signals in addition to those at 19p13.3....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Stryker GmbH

Recalled Item: Nail Insertion Sleeve Recalled by Stryker GmbH Due to The devices have a...

The Issue: The devices have a different inner diameter than the diameter specified on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Straumann USA LLC

Recalled Item: Straumann SCS Screwdriver Recalled by Straumann USA LLC Due to Tip of the...

The Issue: Tip of the screwdriver does not have the correct configuration / profile...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Stryker GmbH

Recalled Item: Nail Insertion Sleeve Recalled by Stryker GmbH Due to The devices have a...

The Issue: The devices have a different inner diameter than the diameter specified on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: 3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60...

The Issue: Telepack may not power on when using the 3AA battery cradle.

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

Class III — Low RiskOngoing
Medical DeviceMay 27, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS pheno- angiography systems developed for single and biplane diagnostic...

The Issue: Software error VE10B -In case of a fault within the drivetrain of an axis...

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

Class II — Potential Health HazardOngoing
DrugMay 26, 2021· McKesson Corporation dba McKesson Drug Company

Recalled Item: Levetiracetam Tablets USP Recalled by McKesson Corporation dba McKesson Drug...

The Issue: Labeling; Wrong Barcode; error in the machine-readable barcode which could...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 26, 2021· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion systems with software release R1.x Recalled by PHILIPS MEDICAL...

The Issue: In the Azurion system, the user can add a new study to a patient by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Philips Healthcare

Recalled Item: Azurion systems with software release R2.0.x Recalled by Philips Healthcare...

The Issue: In the Azurion system, the user can add a new study to a patient by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Owen Mumford USA, Inc.

Recalled Item: Unifine Pentips Plus Recalled by Owen Mumford USA, Inc. Due to Mixed Up. Two...

The Issue: Mixed Up. Two (2) cases of Unifine Pentips Plus 4mm pen needles have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Flowonix Medical Inc

Recalled Item: Physician Order Form (PL-15400-00 Recalled by Flowonix Medical Inc Due to...

The Issue: Physician Order Form (PL-15400-00 Nov 2018) distributed is discontinued due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2021· Medline Industries Inc

Recalled Item: Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Recalled...

The Issue: Potential for mold contamination (Aspergillus vadensis)

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2021· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus Pro - Patient physiological monitor Recalled by Remote Diagnostic...

The Issue: The Tempus Pro (Trizeps 7 only) when used in combination with a specified...

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

Class II — Potential Health HazardOngoing
DrugMay 21, 2021· Hill Dermaceuticals, Inc.

Recalled Item: DermOtic Oil (fluocinolone acetonide oil) 0.01% Ear Drops 20 mL bottles...

The Issue: Presence of Foreign Substance: Potential for broken glass within the glass...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 21, 2021· Reser's Fine Foods, Inc.

Recalled Item: ***Chicken Street Taco Kit with Trays Recalled by Reser's Fine Foods, Inc....

The Issue: Undeclared egg. The cup of Chipotle Crema in the Chicken Street Taco kits...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 21, 2021· GE Healthcare, LLC

Recalled Item: CARESCAPE PDM-Masimo SpO2. Physiological data monitor. Recalled by GE...

The Issue: Masimo SpO2 Saturation Values can become frozen after an extended length of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Titan 3T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Toshiba Vantage Tiitan 1.5T with Standard gradient Recalled by Canon Medical...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Tiitan 1.5T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing