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. 2,642 recalls have been distributed to Oklahoma in the last 12 months.
Showing 8981–9000 of 28,654 recalls
Recalled Item: VIDAS Lyme IgM II (LYM) Recalled by bioMerieux, Inc. Due to bioMerieux has...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS B.R.A.H.M.S. PROCALCITONIN PCT Recalled by bioMerieux, Inc. Due to...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Mumps IgG (MPG) Recalled by bioMerieux, Inc. Due to bioMerieux has...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS SARS-COV-2 IgG Recalled by bioMerieux, Inc. Due to bioMerieux has been...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation/RayPlan versions 4 - 11A Recalled by RAYSEARCH LABORATORIES AB...
The Issue: An issue where the combined density in a dose grid voxel partially covered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS TOXO IgG Avidity (TXGA) Recalled by bioMerieux, Inc. Due to bioMerieux...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The da Vinci Xi and X surgical systems (IS4000 and Recalled by Intuitive...
The Issue: Incorrect expiration date on its package labeling (shipper box and inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Li-Ion Battery Pack Recalled by Datascope Corp. Due to A...
The Issue: A Cardiosave Lithium-Ion Battery Pack used during protocol testing failed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASC PneumoLiner device Recalled by Olympus Corporation of the Americas Due...
The Issue: Due to manufacturing error, the Pneumoliner Bag Distal Tab that exits the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...
The Issue: The firm has confirmed the potential for Atellica CH Urinary/Cerebrospinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5MMX165MM CANNULATED SCREW Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The product label incorrectly indicated that the screws are fully threaded,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advia Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...
The Issue: The firm has confirmed the potential for ADVIA Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIO-RAD BioPlex 2200 Syphilis Total & RPR Calibrator Recalled by Bio-Rad...
The Issue: Due to two issues: 1) Customer complaints associated with greater than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Medical Linear Accelerator (EMLA) Recalled by Elekta, Inc. Due to...
The Issue: There is a risk that the Diode D1 in the Modulator can fail in a destructive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIO-RAD BioPlex 2200 SYPH T PACK Syphilis Total Recalled by Bio-Rad...
The Issue: Due to two issues: 1) Customer complaints associated with greater than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Monaco - Product Usage: used to make treatment plans Recalled by...
The Issue: Contour changes can be saved on an unintended image set. In addition, these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.