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. 2,638 recalls have been distributed to Oklahoma in the last 12 months.
Showing 10161–10180 of 28,654 recalls
Recalled Item: SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray Recalled by...
The Issue: The product may be contaminated with Burkholderia cepacia
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...
The Issue: Customers are being notified of results from a Toxicological Risk Assessment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 4-(Calibrator values for TIBC...
The Issue: Potential total iron-binding capacity (TIBC) results. The VITROS TIBC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct...
The Issue: Teleflex is voluntarily recalling the products above due to customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedSchenker Smart Transport Medium (STM) System: CULTURE MEDIA Recalled by...
The Issue: Discoloration and turbidity were present in the specified lots of STMs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for Recalled by...
The Issue: Contact lenses may be mislabeled with the incorrect lens power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream Dental CS 3600 Single Use Normal Tips Recalled by CARESTREAM...
The Issue: The mirror may become detached and fall from the unit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRECICE PLATE - Product Usage: intended for limb lengthening Recalled by...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRECICE STRYDE - Product Usage: intended for limb lengthening Recalled by...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precice Bone Transport - Product Usage: intended for limb lengthening...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PLEUR-EVAC Thoracic Catheters (CATHETER Recalled by TELEFLEX MEDICAL INC Due...
The Issue: Teleflex is recalling this product due to a lack of assurance of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS SARS-CoV-2 Antigen Reagent Pack - The VITROS Immunodiagnostic...
The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent- In Vitro...
The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valiant Navion Thoracic Stent Graft System. For endovascular repair of...
The Issue: Due to the presence of type IIIb endoleaks, stent fractures, and stent ring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and...
The Issue: The tube holder can separate from the barrier that secures the device to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.