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. 936 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
936 in last 12 months

Showing 46181–46200 of 49,976 recalls

DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Day/Night Cold & Cough Recalled by Novartis...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
DrugMay 15, 2013· Novartis Consumer Health

Recalled Item: Theraflu Nighttime Warming Relief Nighttime Multi-Symptom Cold Recalled by...

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 15, 2013· Sysmex America Inc

Recalled Item: pocH-100i Recalled by Sysmex America Inc Due to The data printed on the...

The Issue: The data printed on the thermal printer may omit a digit or decimal point in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Four Lead TUR irrigation Set Recalled by Baxter Healthcare Corp. Due to A...

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Two Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp. Due...

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Biomet, Inc.

Recalled Item: Superior Approach Resection Guide Assembly. Indicated for primary Recalled...

The Issue: Biomet has initiated this action following an investigation which identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· AGFA Corp.

Recalled Item: AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 Recalled by...

The Issue: Customers could potentially experience intermittent, unintended and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Maytex Corp

Recalled Item: Comfort brand Ear-Loop Face Mask Recalled by Maytex Corp Due to Recent Lab...

The Issue: Recent Lab testing conducted in March 2013 indicates that the product does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Tosoh Smd Inc

Recalled Item: AIA Analyzer Pipette Tips used on Tosoh AIA-2000 Recalled by Tosoh Smd Inc...

The Issue: Visual inspection of the pipette tips indicated that some of the tips were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Four Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp....

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
FoodMay 15, 2013· Arthur Schuman Midwest LLC

Recalled Item: GRATED 2/25 GRANA PADANO Recalled by Arthur Schuman Midwest LLC Due to...

The Issue: Grated Grana Padano Hard Italian Cheese was tested and found to be positive...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 14, 2013· GE Healthcare, LLC

Recalled Item: Canister: CO2 canister with GE part numbers 1407-3200-000 Recalled by GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Optovue, Inc.

Recalled Item: Optovue iVue with Normative Database (NDB) with Software Version 3.0...

The Issue: Colors from the NDB comparison for Ganglion Cell Complex thickness in the...

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

Class III — Low RiskOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH Calibrator 6 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur iPTH Calibrator 2 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 100 Tests Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Edwards Lifesciences, LLC

Recalled Item: QuickDraw Venous Cannula with Insertion Kit. ThruPort Systmes. Models QD22...

The Issue: Edwards is recalling the QuickDraw Venous Cannula due to complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 500 Tests Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Artis zeego x-ray Recalled by Siemens Medical Solutions USA,...

The Issue: Siemens issued a customer safety notice about the overlay of system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2013· Life Technologies Corporation

Recalled Item: HSV 2 Primers Recalled by Life Technologies Corporation Due to Firm received...

The Issue: Firm received complaints that HSV-2 primers failed to amplify HSV-2 DNA.

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

Class II — Potential Health HazardOngoing