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. 2,414 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,414 in last 12 months

Showing 4198142000 of 49,976 recalls

Medical DeviceJune 3, 2014· Instrumentation Laboratory Co.

Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...

The Issue: Potential for sample misidentification.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing Recalled...

The Issue: Swollen acid bottles due to a trace metal contamination in the Acid Reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Recalled...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: Recalled by...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus...

The Issue: Springs contained in the access door hinge assembly on the Walk Away Plus...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid Suture (blue/white) Product Recalled...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Ability Dynamics LLC

Recalled Item: RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use Recalled...

The Issue: Ability Dynamics is recalling RUSH81 Prosthetic Foot because the existing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra S Double Loaded Suture Product Code: 72203854 Fastener...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2014· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Blue Product Recalled by...

The Issue: Sterility of device is compromised due to breach in sterile barrier

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

Class II — Potential Health HazardOngoing
FoodJune 2, 2014· Frito-Lay, Inc

Recalled Item: Oven Baked Lay's BBQ flavor crisps in 1 1/8 oz package Recalled by...

The Issue: Printing error by the packaging manufacturer erroneously added a "GF" symbol...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2014· Alexion Pharmaceuticals, Inc.

Recalled Item: Soliris (eculizumab) Recalled by Alexion Pharmaceuticals, Inc. Due to...

The Issue: Presence of Particulate Matter: Product failed the appearance for the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 30, 2014· Carestream Health Inc.

Recalled Item: KODAK DirectView DR 9000 System Recalled by Carestream Health Inc. Due to A...

The Issue: A control system failure may cause the U-Arm to move downward unexpectedly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Alere San Diego, Inc.

Recalled Item: Alere Triage BNP Calibrators for the Beckman Coulter Access Family Recalled...

The Issue: Alere San Diego is recalling Alere Triage BNP Calibrators for the Beckman...

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

Class III — Low RiskOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2014· Instrumed International, Inc.

Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...

The Issue: Additional caution statements have been added to the Instructions For Use...

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

Class II — Potential Health HazardOngoing