Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cook Spectrum Minocycline/Rifampin Impregnated Double Lumen Central Venous Catheter Tray Recalled by Cook Inc. Due to Cook Medical has received reports of the trays...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Cook Inc. directly.
Affected Products
Cook Spectrum Minocycline/Rifampin Impregnated Double Lumen Central Venous Catheter Tray Cook Spectrum Minocycline/Rifampin Impregnated Triple Lumen Central Venous Catheter Tray
Quantity: 99 units
Why Was This Recalled?
Cook Medical has received reports of the trays containing the incorrect needle, which in some cases could result in the inability to pass a wire guide through the needle. Potential adverse events that may occur as a result of utilizing needles of incorrect size include delay in treatment, which could be critical in an emergent situation. There have been no reports of illness or injury associated with this issue.
Where Was This Sold?
This product was distributed to 16 states: AZ, CA, GA, IL, LA, MN, MS, NV, NY, NC, OK, PA, TN, TX, WI, DC
About Cook Inc.
Cook Inc. has 262 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report